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House mouse
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House mouse
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Rodentia
Family: Muridae
Genus: Mus
Subgenus: Mus
Species:
M. musculus
Binomial name
Mus musculus
Subspecies
House mouse range (note: distribution is incomplete)
Synonyms

Mus abbotti

The house mouse (Mus musculus) is a small mammal of the rodent family Muridae, characteristically having a pointed snout, large rounded ears, and a long and almost hairless tail. It is one of the most abundant species of the genus Mus. Although a wild animal, the house mouse has benefited significantly from associating with human habitation to the point that truly wild populations are significantly less common than the synanthropic populations near human activity.

The house mouse has been domesticated as the pet or fancy mouse, and as the laboratory mouse, which is one of the most important model organisms in biology and medicine. The complete mouse reference genome was sequenced in 2002.[3][4]

Characteristics

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The house mouse is best identified by the sharp notch in its upper front teeth.
Skull of Mus musculus - MHNT

House mice have an adult body length (nose to base of tail) of 7.5–10 centimetres (3–4 in) and a tail length of 5–10 cm (2–4 in). The weight is typically 11–30 g (38–1 oz). In the wild they vary in color from grey and light brown to black (individual hairs are actually agouti coloured), but domesticated fancy mice and laboratory mice are produced in many colors ranging from white to champagne to pink. They have short hair and some, but not all, sub-species have a light belly.[5] The ears and tail have little hair. The hind feet are short compared to Apodemus mice, only 15–19 mm (91634 in) long; the normal gait is a run with a stride of about 4.5 cm (1+34 in), though they can jump vertically up to 45 cm (18 in).[6] The voice is a high-pitched squeak.[7][8] House mice thrive under a variety of conditions; they are found in and around homes and commercial structures, as well as in open fields and agricultural lands.[9]

Newborn males and females can be distinguished on close examination as the anogenital distance in males is about double that of the female.[10] From the age of about 10 days, females have five pairs of mammary glands and nipples; males have no nipples.[11] When sexually mature, the most striking and obvious difference is the presence of testicles on the males. These are large compared to the rest of the body and can be retracted into the body.[12]

The tail, which is used for balance,[13][14][15] has only a thin covering of hair as it is the main peripheral organ of heat loss in thermoregulation[14] along with—to a lesser extent—the hairless parts of the paws and ears. Blood flow to the tail can be precisely controlled in response to changes in ambient temperature using a system of arteriovenous anastomoses to increase the temperature of the skin on the tail by as much as 10 °C (10 K; 18 °F) to lose body heat.[16] Tail length varies according to the environmental temperature of the mouse during postnatal development, so mice living in colder regions tend to have shorter tails.[5] The tail is also used for balance when the mouse is climbing or running, or as a base when the animal stands on its hind legs (a behaviour known as tripoding), and to convey information about the dominance status of an individual in encounters with other mice.[17]

In addition to the regular pea-sized thymus organ in the chest, house mice have a second functional pinhead-sized thymus organ in the neck next to the trachea.[18]

Taxonomy and subspecies

[edit]
Euarchontoglires
Glires

Rodentia (rodents)

Lagomorpha (rabbits, hares, pikas)

Euarchonta
Japanese house mouse (M. m. molossinus)

Mice are boreoeutherian placental mammals of the Glires clade, which means they are amongst the closest relatives of humans other than lagomorphs, treeshrews, flying lemurs and other primates.

The three widely accepted subspecies are increasingly treated as distinct species by some:[19][20]

  • Southeastern Asian house mouse (M. m. castaneus) (southern and southeastern Asia)
  • Western European house mouse (M. m. domesticus); includes the fancy mouse and the laboratory mouse (Western Europe, North America, South America, Africa and Oceania)
  • Eastern European house mouse (M. m. musculus) (Eastern Europe and northern Asia)

Two additional subspecies have been recognized more recently:[20]

  • Southwestern Asian house mouse (M. m. bactrianus) (southwestern and Central Asia). However, due to significant genetic similarity observed between M. m. bactrianus and M. m. castaneus, the subspecies designation for M. m. bactrianus has now been questioned.[2]
  • Pygmy house mouse (M. m. gentilulus) (the Arabian Peninsula and Madagascar)[21]

Many more subspecies' names have been given to house mice, but these are now regarded as synonyms of the five subspecies. Some populations are hybrids of different subspecies, including the Japanese house mouse (M. m. molossinus).[20] A notable region of hybridization is a region in general Europe where M. m. domesticus and M. m. musculus are often found to hybridize.[22] However, male hybrid mice typically experience hybrid sterility, which maintains reproductive separation between the two subspecies.[23]

Chromosomal races

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The standard species karyotype is composed of 40 chromosomes. Within Western Europe there are numerous populations – chromosomal races – with a reduced chromosome count arising from Robertsonian fusion.

Evolution

[edit]

Suzuki et al., 2013 confirms the theory that M. musculus originates in Southwestern Asia and identifies 5 subspecies and their origins: musculus in northern Eurasia, castaneus in India and Southeast Asia, a previously unknown subspecies from Nepal, domesticus in western Europe, and gentilulus in Yemen.[24]

A recent study using 89 whole-genome sequences revealed that the modern day M. m. castaneus emerged from an ancestral M. musculus population in Indian subcontinent some time around 700 kya. From there, this ancestral population migrated to Iran around 360 kya to form M. m. domesticus and then to Afghanistan around 260 kya to form M. m. musculus.[25]

Behavior

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A house mouse feeding

House mice usually run, walk, or stand on all fours, but when eating, fighting, or orienting themselves, they rear up on their hind legs with additional support from the tail – a behavior known as "tripoding". Mice are good jumpers, climbers, and swimmers, and are generally considered to be thigmotactic, i.e. usually attempt to maintain contact with vertical surfaces.[citation needed]

Mice are mostly crepuscular or nocturnal; they are averse to bright lights. The average sleep time of a captive house mouse is reported to be 12.5 hours per day.[citation needed] They live in a wide variety of hidden places near food sources, and construct nests from various soft materials. Mice are territorial, and one dominant male usually lives together with several females and young mice. Dominant males respect each other's territories and normally enter another's territory only if it is vacant. If two or more males are housed together in a cage, they often become aggressive unless they have been raised together from birth.[citation needed]

House mice primarily feed on plant matter, but are omnivorous.[26] They eat their own faeces to acquire nutrients produced by bacteria in their intestines.[27] House mice, like most other rodents, do not vomit.[28]

Mice are generally afraid of rats which often kill and eat them, a behavior known as muricide. Despite this, free-living populations of rats and mice do exist together in forest areas in New Zealand, North America, and elsewhere. House mice are generally poor competitors and in most areas cannot survive away from human settlements in areas where other small mammals, such as wood mice, are present.[29] However, in some areas (such as Australia), mice are able to coexist with other small rodent species.[30]

Social behavior

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The social behavior of the house mouse is not rigidly fixed into species-specific patterns but is instead adaptable to the environmental conditions, such as the availability of food and space.[31][32] This adaptability allows house mice to inhabit diverse areas ranging from sandy dunes to apartment buildings.[31]

House mice have two forms of social behaviour, the expression of which depends on the environmental context. House mice in buildings and other urbanized areas with close proximity to humans are known as commensal.[31] Commensal mice populations often have an excessive food source resulting in high population densities and small home ranges. This causes a switch from territorial behaviour to a hierarchy of individuals.[31][33] When populations have an excess of food, there is less female-female aggression, which usually occurs to gain access to food or to prevent infanticide.[31] Male-male aggression occurs in commensal populations, mainly to defend female mates and protect a small territory.[31][32] The high level of male-male aggression, with a low female-female aggression level is common in polygamous populations.[34] The social unit of commensal house mouse populations generally consists of one male and two or more females, usually related.[34][35] These groups breed cooperatively, with the females communally nursing. This cooperative breeding and rearing by related females helps increase reproductive success. When no related females are present, breeding groups can form from non-related females.[35]

In open areas such as shrubs and fields, the house mouse population is known as noncommensal. These populations are often limited by water or food supply and have large territories.[32] Female-female aggression in the noncommensal house mouse populations is much higher, reaching a level generally attributed to free-ranging species. Male aggression is also higher in noncommensal populations. In commensal populations, males come into contact with other males quite frequently due to high population densities and aggression must be mediated or the risk of injury becomes too great.[31]

Both commensal and noncommensal house mouse males aggressively defend their territory and act to exclude all intruders. Males mark their territory by scent marking with urine. In marked territories, intruders showed significantly lower aggression than the territory residents.[32] House mice show a male-biased dispersal; males generally leave their birth sites and migrate to form new territories whereas females generally stay and are opportunistic breeders rather than seasonal.[36]

Senses and communication

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Vision

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An adult house mouse

The visual apparatus of mice is basically similar to that of humans but differs in that they are dichromats and have only two types of cone cells whereas humans are trichromats and have three. This means that mice do not perceive some of the colors in the human visual spectrum.[37] However, the ventral area of the mouse retina has a much greater density of ultraviolet-sensitive cones than other areas of the retina, although the biological significance of this structure is unknown.[38][39][40] In 2007, mice genetically engineered to produce the third type of cone were shown to be able to distinguish a range of colors similar to that perceived by tetrachromats.[37]

Olfaction

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House mice also rely on pheromones for social communication, some of which are produced by the preputial glands of both sexes. The tear fluid and urine of male mice also contains pheromones, such as major urinary proteins.[41][42] Mice detect pheromones mainly with the vomeronasal organ (Jacobson's organ), located at the bottom of the nose.

The urine of house mice, especially that of males, has a characteristic strong odor. At least 10 different compounds, such as alkanes, alcohols, etc., are detectable in the urine. Among them, five compounds are specific to males, namely 3-cyclohexene-1-methanol, aminotriazole (3-amino-s-triazole), 4-ethyl phenol, 3-ethyl-2,7-dimethyl octane and 1-iodoundecane.[43]

Odours from adult males or from pregnant or lactating females can speed up or retard sexual maturation in juvenile females and synchronise reproductive cycles in mature females (i.e. the Whitten effect). Odours of unfamiliar male mice may terminate pregnancies, i.e. the Bruce effect.

Tactile

[edit]

Mice can sense surfaces and air movements with their whiskers which are also used during thigmotaxis. If mice are blind from birth, super-normal growth of the vibrissae occurs presumably as a compensatory response.[44] Conversely, if the vibrissae are absent, the use of vision is intensified.[45]

Life cycle and reproduction

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A newborn mouse
A two-week-old fancy mouse, just about to open its eyes

Female house mice have an estrous cycle about four to six days long, with estrus itself lasting less than a day. If several females are held together under crowded conditions, they will often not have an estrus at all. If they are then exposed to male urine, they will come into estrus after 72 hours.[citation needed]

Male house mice court females by emitting characteristic ultrasonic calls in the 30 kHz–110 kHz [citation needed] range. The calls are most frequent during courtship when the male is sniffing and following the female; however, the calls continue after mating has begun, at which time the calls are coincident with mounting behaviour. Males can be induced to emit these calls by female pheromones. The vocalizations appear to differ between individuals and have been compared to bird songs because of their complexity.[46] While females have the capability to produce ultrasonic calls, they typically do not do so during mating behaviour.[citation needed]

Following copulation, female mice will normally develop a mating plug which prevents further copulation. The plug is not necessary for pregnancy initiation, as this will also occur without the plug. The presence or absence of the plug will not affect litter size either.[47] This plug stays in place for some 24 hours. The gestation period is about 19–21 days, and they give birth to a litter of 3–14 young (average six to eight). One female can have 5 to 10 litters per year, so the mouse population can increase very quickly. Breeding occurs throughout the year. (However, animals living in the wild do not reproduce in the colder months, even though they do not hibernate.)[citation needed]

The pups are born blind and without fur or ears. The ears are fully developed by the fourth day, fur begins to appear at about six days and the eyes open around 13 days after birth; the pups are weaned at around 21 days. Females reach sexual maturity at about six weeks of age and males at about eight weeks, but both can copulate as early as five weeks.[48]

Polygamy

[edit]

Although house mice can be either monogamous or polygamous, they are most commonly polygamous. They generally show characteristics of mate-defense polygyny in that males are highly territorial and protective of their mates, while females are less agonistic.[49] The communal nursing groups that result from these behaviors lead to lower numbers of infanticide since more females are able to protect greater numbers of offspring.[50]

Evolutionary and behavioural consequences

[edit]

Both evolutionary and behavioral consequences result from the polygamous nature of the house mouse. One consequence is the paternal investment, which is lower in polygamous mice than in mice that are monogamous.[51] This occurs due to the fact that males spend more time involved in sexual competition than do females, leaving less time for paternal care.[51] Polygamous male house mice spend less time alone with pups.[51] They are also less likely and slower to retrieve lost pups than males of monogamous mice.[51] In contrast, the maternal investment is similar between female mice that have mated once versus multiply.[51]

The polygamous behavior of female house mice promotes sperm competition, which affects both male and female evolutionary fitness.[47] Females who mate with multiple males tend to produce both pups in greater numbers,[47] and with higher survival rates,[52] increasing female fitness. Sperm competition that arises from polygamy favors males with faster, more motile sperm in higher numbers, increasing male fitness.[47] The competitive aspect of insemination increases the frequency of polyandrous events and fertilizations. Polyandry has evolved to increase reproductive success.[53] Male mating behavior is also affected in response to the practice of polygamous behavior. Compared to monogamous house mice, polygamous house mice mate for longer periods of time.[54] This behaviour allows for an increase in both the transfer of sperm and paternity success, which in turn increases male fitness.[54]

Polyandry

[edit]

As opposed to polygyny, polyandrous behavior in females is the act of breeding with several males in the same season.[55] Variation in number of males that females mate with occurs among a population. Polyandrous behavior is a common mating pattern in the subspecies M. m. musculus as well as its relative M. m. domesticus.[55]

Polyandry occurs in 30% of all wild populations of house mice.[56] Litters from multiple sires tend to be more genetically diverse than litters of single sires.[55] Multiple paternity is also more common in larger populations than smaller populations, because there is a larger number of mates and more diverse mates to choose from.[56] Within a population, males and females show different levels of multiple mating. Females show bias toward unrelated males rather than related males during sexual selection, resulting in more genetically diverse offspring and a reduction of inbreeding depression. Inbreeding depression increases genetic incompatibilities, levels of homozygosity, and the chance of expression of deleterious recessive alleles.[53] Polyandry has been shown to increase offspring survival compared to monandry.

Evolutionary consequences

[edit]

The fitness of females increases in polyandrous lines due to more genetic diversity and greater litter size.[47]

Due to polyandry, males can be confused by the identity of new offspring. Multiple mating by females and paternity confusion can decrease rates of infanticide. If the males are uncertain if the offspring are theirs, they are less likely to kill the offspring.[57]

Intrauterine insemination causes an evolutionary consequence resulting from polyandrous behavior. When multiple males mate with one female, there are multiple sets of sperm gametes in a female mouse. Offspring fertilized by multiple males can compete more strongly for mother's resources and can lead to a decrease in body size and variation in body size.[58]

Inbreeding avoidance

[edit]

Since inbreeding is detrimental, it tends to be avoided. In the house mouse, the major urinary protein (MUP) gene cluster provides a highly polymorphic scent signal of genetic identity that appears to underlie kin recognition and inbreeding avoidance. Thus there are fewer matings between mice sharing MUP haplotypes than would be expected if there were random mating.[59] Another mechanism for avoiding inbreeding is evident when a female house mouse mates with multiple males. In such a case, there appears to be egg-driven sperm selection against sperm from related males.[60]

Genetics

[edit]

As a model organism, a great deal is known about mouse genetics, with a major tool being the knockout mouse technique.

Life expectancy

[edit]
In both agricultural and urban environments house mice are often preyed upon by the domestic cat, as with this ragdoll, seen here playing with a mouse it has caught.

House mice usually live less than one year in the wild, due to a high level of predation and exposure to harsh environments.[61] In protected environments, however, they often live two to three years. The Methuselah Mouse Prize is a competition to breed or engineer extremely long-lived laboratory mice. As of 2005, the record holder was a genetically engineered mouse that lived for 1,819 days (7 days short of 5 years).[62] Another record holder that was kept in an enriched environment but did not receive any genetic, pharmacological, or dietary treatment lived for 1,551 days (4 years, 90 days).[63][64]

Aging

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In several different mouse strains, a significant increase was observed with age in 8-Oxo-2'-deoxyguanosine (8-oxo-dG) levels in nuclear DNA from liver, heart, brain, kidney, skeletal muscle and spleen. This increase in DNA damage was attributed to an age related increase in the sensitivity of these tissues to oxidative stress. Dietary restriction is known to increase the lifespan of rodents and to retard aging. Dietary restriction was found to significantly reduce the age-related accumulation of 8-oxo-dG levels in nuclear DNA of all tissues studied in mice.[65] Thus it was suggested that oxidative DNA damages that arise from normal cellular metabolism could be highly relevant to aging and the diseases of aging.[65] In another study, two types of DNA damage (8-hydroxy-2'-deoxyguanosine and DNA-protein crosslinks) were found to increase with age in mouse brain and liver.[66]

Mice and humans

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History

[edit]

House mice usually live in proximity to humans, in or around houses and/or fields. They are native to India,[67][68] and later they spread to the eastern Mediterranean about 13,000 BC, only spreading into the rest of Europe around 1000 BC. This time lag is thought to be because the mice require agrarian human settlements above a certain size.[69] The house mouse first arrived in the Americas in the early sixteenth century. It was carried aboard on the ships of Spanish explorers and Conquistadors. About one hundred years later, it arrived in North America with French fur traders and English colonists. They have since been spread to all parts of the globe by humans.[70]

Many studies have been done on mouse phylogenies to reconstruct early human movements. For example, one study suggests the possibility of a previously unsuspected early link between Northern Europe and Madeira on the basis of the origin of Madeiran mice.[71] House mice were thought to be the primary reason for the domestication of cats.[72]

As pets

[edit]
Fancy mice may be of colours and/or have markings not found in wild mice

The first written reference to mice kept as pets occurs in the Erya, the oldest extant Chinese dictionary, from a mention in an 1100 BC version.[73] Human domestication led to numerous strains of "fancy" or hobby mice with a variety of colours and a docile temperament. Domestic varieties of the house mouse are bred as a food source for some carnivorous pet reptiles, birds, arthropods, and fish.[74] The effects of domestication can be rapid, with captive-reared mice differing in boldness and activity patterns compared to wild-caught mice after 4–5 generations in recent research.[75][76]

Mice as pests

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Infestation of mice. Taxidermy display, Staatliches Museum für Naturkunde Karlsruhe, Germany.

Mice are widespread pest organisms, and one of the most common rodents to infest human buildings. They commonly forage outdoors during the spring and summer, but retreat into buildings through the autumn and winter to seek warmth and food. They typically feed on unattended food, leftovers and garden produce. Their foraging risks the contamination and degradation of food supplies, and can also spread other pests such as fleas, ticks, lice and mites.[77]

When infesting homes, house mice may pose a risk of damaging and compromising the structure of furniture and the building itself. They gnaw various materials to file down their growing teeth and keep the length under control. Common damage includes gnawed electrical wires, marks on wooden furniture and construction supporting elements, and textile damage.[78]

Mice and diseases

[edit]

House mice can sometimes transmit diseases, contaminate food, and damage food packaging. Although the Centers for Disease Control and Prevention provides a list with diseases transmitted by rodents,[79] only a few of the diseases are transmitted through the house mouse.[80]

Lymphocytic choriomeningitis (LCMV) can be transmitted by mice, but is not a commonly reported infection in humans, though most infections are mild and are often never diagnosed.[81][82][83] Some concern exists that women should not be infected with LCMV during pregnancy.[84][85]

House mice are not usually a vector of human plague (bubonic plague) because they have fewer infestations with fleas than do rats, and because the fleas which house mice normally carry exhibit little tendency to bite humans rather than their natural host.[86]

Rickettsialpox, caused by the bacterium Rickettsia akari and similar to chickenpox, is spread by mice in general, but is very rare and generally mild and resolves within two or three weeks if untreated. No known deaths have resulted from the disease. Murine typhus (also called endemic typhus), caused by the bacterium Rickettsia typhi, is transmitted by the fleas that infest rats. While rat fleas are the most common vectors, cat fleas and mouse fleas are less common modes of transmission.[87] Endemic typhus is highly treatable with antibiotics. The U.S. CDC currently does not mention rickettsialpox or murine typhus on its website about diseases directly transmitted by rodents (in general).[79]

Leptospirosis is carried by a variety of wild and domestic animals including dogs, rats, swine, cattle, mice in general, and can be transmitted by the urine of an infected animal and is contagious as long as the urine is still moist.[88]

In Central Europe, the Dobriva sequence of hantavirus has been found in house mice. This is the most serious type of hanta that can infect humans.[89]

Mice contribute indirectly to the transmission of Lyme disease by acting as hosts for tick larvae.[90] When young ticks feed on infected mice, they acquire the bacteria responsible for the disease. As these ticks mature, they can transmit the infection to humans and other animals through subsequent bites, thereby playing a crucial role in the disease's ecological cycle.[91]

Invasive species

[edit]

Mice have become an invasive species on islands to where they have spread during the period of European exploration and colonisation.[92]

New Zealand had no land mammals other than two species of bat prior to human occupation, and the house mouse is one of many species that have been introduced. Mice are responsible for a reduction in native bird species since they eat some of the same foods as birds. They are also known to kill lizards and have a large effect on native insects.[93]

Gough Island in the South Atlantic is used by 20 species of seabirds for breeding, including almost all of the world's Tristan albatross (Diomedea dabbenena) and Atlantic petrel (Pterodroma incerta). Until house mice arrived on the island in the 19th century with sailors, the birds did not have any mammalian predators. The mice have since grown unusually large and have learned to attack albatross chicks, which can be 90 cm tall, but are largely immobile, by working in groups and gnawing on them until they bleed to death.[94]

In the grain belt of southeastern Australia, the introduced subspecies M. m. domesticus breed so successfully, every three years or so they reach plague proportions, achieving densities of 1000 per hectare and causing massive disruption to communities, and losses to agriculture of A$36 million annually.[95]

As a model organism

[edit]
An individually ventilated and sealed cage for laboratory mice

Mice are the most commonly used mammalian laboratory animal, due to their relatively close relationship, and associated high homology, with humans, their ease in maintenance and handling, and their high rate of reproduction. Laboratory mice typically belong to standardized inbred strains selected for the stability or clarity of specific harmful mutations. This allows research with laboratory mice to easily restrict genetic and biological variables, making them very useful model organisms in genetic and medicinal research.[96] Mice have been used in scientific research since the 1650s.[97]

In folk culture

[edit]

Importance of mice as a house and agricultural pest resulted in a development of a variety of mouse-related rituals and stories in world's cultures. The Ancient Egyptians had a story about "The mouse as vizier".[98]

Many South Slavs had a traditional annual "Mouse Day" celebration. In the eastern Balkans (most of Bulgaria, North Macedonia, the Torlak districts of Serbia), the "Mouse Day" (Bulgarian: Миши ден, Мишин ден) was celebrated on 9 October of the Julian calendar (corresponds to 27 October of the Gregorian calendar in the 20th and 21st centuries), the next day after the feast of Saint Demetrius. In the western Balkans (Bosnia, Croatia), the Mouse Day would usually be celebrated in the spring, during the Maslenitsa week or early in the Lent.[99]

See also

[edit]

References

[edit]

Further reading

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
The house mouse (Mus musculus) is a small belonging to the family , characterized by a body length of 65–95 , a nearly as long (60–105 ), and a weight of 12–30 g, with fur typically light brown to black on the upper body and white or buffy on the underparts, along with large rounded ears and a pointed snout. Native to regions from the Mediterranean to , it has become a cosmopolitan through human-mediated dispersal, thriving as a commensal in structures worldwide. This adaptability, combined with its short generation time and genetic similarity to humans (sharing about 85–95% of genes), makes it one of the most important model organisms in biomedical research for studying , , and diseases. House mice prefer habitats closely associated with humans, such as homes, barns, warehouses, and agricultural fields, where they commonly nest in burrows, wall voids, or sheltered spots using materials like grass, cloth, or paper. In wall cavities and voids, they can survive and thrive by opportunistically consuming insects (such as cockroaches, beetle larvae, and caterpillars) and other available scraps, particularly when preferred food sources are limited. They can also occupy natural environments like grasslands, forests, and deserts, ranging from sea level to elevations over 4,000 m and across diverse climates from tropical to subarctic, though they rarely persist far from human influence in undisturbed wild areas. Omnivorous feeders, they consume seeds, grains, insects, and occasionally carrion in the wild, but in human settings, they target stored foods, crumbs, and even non-food items like glue or soap, often storing excess in hidden caches. Behaviorally, house mice are primarily nocturnal and exhibit a mix of territoriality and colonial living, with males establishing dominance hierarchies and females forming looser social groups; they communicate via ultrasonic vocalizations, pheromones, and scent marking. is prolific, occurring year-round in favorable conditions with 5–14 litters annually, each producing 3–12 young after a 19–21 day ; offspring reach in 5–7 weeks, contributing to lifespans averaging 1–2 years in the wild but up to 6 years in captivity. As pests, house mice cause significant economic damage by contaminating food supplies, gnawing on structures, and transmitting diseases such as salmonellosis, lymphocytic choriomeningitis (LCMV), and murine typhus through urine, feces, or bites. Conversely, their utility in laboratory settings has revolutionized fields like , , and , with inbred strains enabling precise genetic manipulations and over 25,000 mouse-related publications annually advancing human health insights.

Taxonomy and evolution

Classification and subspecies

The house mouse (Mus musculus Linnaeus, 1758) is a species within the genus Mus and the family Muridae, part of the order Rodentia in the class Mammalia. This classification places it among the Old World rats and mice, characterized by its association with human habitats and adaptability to diverse environments. The species is divided into several subspecies, primarily distinguished by geographic ranges and genetic markers, with three main ones widely recognized: M. m. domesticus, M. m. musculus, and M. m. castaneus. M. m. domesticus, known as the Western European house mouse, is native to , , and the , from where it has been introduced globally, often thriving in commensal settings near human settlements. M. m. musculus, the Eastern house mouse, occupies , , and extends into , typically in cooler, more continental climates. M. m. castaneus, the Southeastern Asian house mouse, is distributed across southern and southeastern , including , southern , and Southeast Asian islands, showing the highest genetic diversity among the subspecies. These subspecies display subtle morphological variations, such as differences in relative tail length (longer in M. m. domesticus compared to M. m. castaneus) and ear size proportions, which correlate with their adaptive ranges but are less pronounced than genetic distinctions. Chromosomal variations, including karyotypic differences, further delineate subspecies boundaries. Recent genetic studies in the , leveraging whole-genome sequencing and phylogenomic analyses, have affirmed the divergence of these core around 0.3–0.5 million years ago while revealing ongoing hybridization in contact zones that challenge strict boundaries. For instance, investigations across have identified patterns and potential new lineages, such as M. m. gyirongus in the Tibetan region, refining taxonomic understanding without overturning the primary classifications. These findings underscore the role of human-mediated dispersal in shaping distributions.

Chromosomal races

The house mouse (Mus musculus) typically possesses a standard diploid chromosome number of 2n=40, comprising 38 acrocentric autosomes and one pair of , with all autosomes featuring centromeres positioned near one end. This baseline is widespread, but cytogenetic diversity is prominent due to Robertsonian (Rb) fusions, a common rearrangement in which the long arms of two acrocentric s fuse at their centromeres, resulting in a single metacentric with the short arms often lost. Each such fusion reduces the diploid number by one, leading to homozygous Rb races with 2n ranging from 22 to 40, while hybrid zones exhibit intermediate counts in heterozygotes, such as 2n=24 to 32, where metacentric and acrocentric chromosomes coexist and form multivalent configurations during . These variations underscore the role of chromosomal polymorphisms in population differentiation. In European hybrid zones, this cytogenetic variability is particularly evident, with distinct races interbreeding and producing offspring with mixed morphologies. For example, in the Danish hybrid zone, standard 2n=40 acrocentric mice from M. m. domesticus overlap with Rb races carrying multiple metacentric fusions, resulting in heterozygotes that display reduced fertility due to meiotic complications from trivalent or quadrivalent pairings. Similarly, in the Aeolian near , , multiple Rb races with unique combinations of metacentrics, such as fusions involving chromosomes 1, 6, 8, 10, 12, 13, 15, and 18, form staggered hybrid zones where acrocentric and metacentric forms hybridize, contributing to a of karyotypes from 2n=24 to 40. These zones highlight how Rb polymorphisms maintain genetic structure despite . Recent studies from 2023 to 2025 have elucidated the mechanisms by which these rearrangements promote , emphasizing their impact on and fertility. A 2025 analysis of spermatocytes revealed significantly lower crossover frequencies in Rb homozygotes (2n=24; average 20.1 crossovers per cell) and heterozygotes (2n=32; 22.4 crossovers) compared to standard homozygotes (2n=40; 26 crossovers), attributed to pericentromeric interference that suppresses recombination and elevates by up to 66% in heterozygotes, thereby reducing hybrid viability. Complementing this, a 2024 study showed that Rb fusions interact with allelic variation in the Prdm9 gene to reshape genome-wide recombination landscapes, suppressing exchanges in fused regions and facilitating the accumulation of incompatible alleles that strengthen postzygotic barriers. Specific fusions like Rb(16.17), which joins the long arms of chromosomes 16 and 17 into a metacentric, exemplify this by causing meiotic instability in heterozygotes, further driving in hybrid zones. These findings are most prevalent in M. m. domesticus, where Rb races with elevated fusion rates predominate.

Evolutionary origins

The house mouse (Mus musculus) belongs to the Mus within the Muridae, with its lineage diverging from other Mus species, such as M. spretus and M. spicilegus, approximately 1.5–2 million years ago based on estimates from mitochondrial and nuclear DNA analyses. This divergence occurred during the Pliocene-Pleistocene transition, reflecting broader rodent radiations in amid climatic shifts that fragmented habitats and promoted . The M. musculus species itself emerged from wild ancestors in around 500,000 years ago, with phylogroups tracing back to regions like northern , , and , where arid steppes and semi-desert environments favored small, adaptable murids. Key evolutionary milestones for M. musculus involve the transition to , beginning approximately 15,000 years ago in the during the Epipaleolithic period, when settled communities like the Natufians created stable food stores that attracted wild mice. This association intensified around 10,000–12,000 years ago with the advent of agriculture in the , providing abundant cereal grains and shelter that selected for traits enabling close human proximity, such as reduced fear responses and enhanced foraging in anthropogenic niches. Human migrations subsequently facilitated the global dispersal of these commensal populations, with house mice hitching rides on trade routes, ships, and settlements from to , , and the over the past 10,000 years. Genetic studies have illuminated admixture events shaping M. musculus to human environments, revealing between eastern and western phylogroups during post-glacial expansions that gave rise to modern . These findings underscore how human-induced ecological pressures drove rapid genomic changes, with admixture contributing to hybrid vigor and broader environmental tolerance in house mouse populations.

Physical characteristics

Morphology and size

The house mouse (Mus musculus) is a small with an adult body length ranging from 7.5 to 10 cm (nose to base of tail), a tail length of 5 to 10 cm, and a weight typically between 12 and 30 grams. These measurements can vary slightly by and population, with adults averaging around 17 to 25 grams in weight. There is modest in size, with males generally larger than females, though the difference is subtle and often less pronounced in commensal populations. Key anatomical features include large, rounded ears. The tail is long and nearly hairless, covered in scales, serving functions in balance during movement and by adjusting blood flow to control heat loss, though its contribution to overall body heat dissipation is relatively modest at 5-8%. Prominent sharp incisors, characteristic of , are chisel-shaped with hardened enamel on the front surfaces, enabling effective gnawing on hard materials to maintain length as they continuously grow. Locomotion is primarily quadrupedal, supporting rapid running, jumping, and swimming, with notable agility in climbing vertical surfaces due to flexible limbs and strong gripping claws. Size variations in house mice often follow ecogeographic patterns, such as , where individuals in colder climates exhibit larger body sizes to conserve heat, as observed in introduced populations across latitudes. This is driven more by genetic selection than environmental plasticity, highlighting the ' responsiveness to climatic gradients.

Coloration and adaptations

The house mouse (Mus musculus) typically displays a grayish-brown on the dorsal surface with a paler, often white or gray, ventral side, creating effective in varied environments. This coloration arises from the wild-type pattern, characterized by individual hairs that are banded with alternating yellow pheomelanin and black eumelanin pigments, produced under the influence of the . The dorsal-ventral contrast results from region-specific expression of the agouti gene, which modulates pigment deposition during development. Color variations occur due to genetic mutations, particularly in laboratory strains. Albino variants, lacking melanin production due to mutations in the tyrosinase gene (Tyr), result in white fur and pink eyes, as seen in strains like BALB/c. Black coats, caused by recessive alleles at the agouti locus (a/a) combined with dominant black pigment genes, are prominent in strains such as C57BL/6. These mutations, while rare in wild populations, highlight the genetic plasticity underlying coat diversity. A 2023 study analyzing haplotypes in a gene-rich region including Mc1r (melanocortin 1 receptor) revealed genetic structure associated with dorsal coat color variation in Asian house mouse subspecies, suggesting evolutionary divergence in pigmentation. Physiological adaptations enhance survival across habitats. The dense underfur traps air for thermal insulation, reducing heat loss and aiding thermoregulation in fluctuating temperatures. Long, specialized whiskers (vibrissae) on the snout and face, embedded in highly innervated follicles, serve as tactile sensors for spatial navigation in confined or dark spaces. The skeleton's flexibility, facilitated by a compressible ribcage and reduced clavicles, allows the body to deform and pass through openings as small as 6 mm—roughly the diameter of a pencil—enabling exploitation of narrow crevices in urban and natural settings.

Sensory and communication systems

Vision

The house mouse (Mus musculus) possesses dichromatic vision, relying on two types of cone photoreceptors: short-wavelength-sensitive (SWS) cones tuned to (UV) light around 360 nm and medium-wavelength-sensitive (MWS) cones sensitive to light around 508 nm. This UV sensitivity is facilitated by the SWS1 gene, which enables detection of UV wavelengths that are invisible to humans, while the overall color discrimination is limited to distinguishing between these short (UV) and medium () spectra, analogous to a blue-yellow axis in other dichromats. The eyes are proportionally large relative to the head size, a common in nocturnal and crepuscular mammals that enhances capture in dim environments. The retinal structure of the house mouse is optimized for low-light conditions, featuring a high of rod photoreceptors that constitute approximately 97% of all photoreceptors, with rod densities averaging around 437,000 cells per mm². This rod dominance supports scotopic (night) vision but results in poor , estimated at about 0.5 cycles per degree—roughly 1/100th to 1/120th the resolution of human vision (30–60 cycles per degree)—limiting the ability to resolve fine spatial details. Consequently, house mice exhibit limited color beyond the UV-green dichotomy and prioritize motion detection over static fine detail in their visual processing. Behavioral studies highlight the functional role of this , particularly the UV sensitivity confirmed by analyses of , which aids in detecting UV-reflective trails left by conspecifics for and territorial marking. This visual cue integrates briefly with olfactory signals to facilitate trail following in low-light settings.

Olfaction and pheromones

The dominates sensory perception in house mice, enabling them to navigate complex environments, identify food sources, and mediate social interactions through chemical cues far more effectively than vision or other senses. This reliance on olfaction is supported by a encoding over 1,000 olfactory receptor genes, which allow for the detection of thousands of distinct odorants. The main , located in the , processes general volatile scents from the environment, while the , an accessory structure in the , specializes in detecting pheromones and non-volatile chemical signals critical for reproductive and agonistic behaviors. Pheromones play a central role in chemical communication among house mice, with urinary signals serving as key markers for territory defense and individual recognition. Major urinary proteins (MUPs), lipocalin family members abundant in male urine, bind and release volatile ligands to signal dominance and provoke in conspecific males; for instance, a specific cluster of four MUP isoforms elicits aggressive responses via vomeronasal detection. These urinary pheromones also facilitate , as females preferentially select males based on scent profiles indicating genetic compatibility, and enable to avoid through discrimination of familial odors. Recent research has elucidated the genetic underpinnings of variation, identifying volatile organic compounds (VOCs) in and body s that differ systematically by , strain, and genetic background. A 2024 study analyzing inbred and wild mouse conspecific scents via revealed that specific VOCs, such as branched-chain fatty acids and sulfur-containing compounds, discriminate individuals and populations, with profiles influenced by (MHC) haplotypes that link diversity to immune gene variation for enhanced mate selection. These MHC-associated profiles underscore how genetic factors shape chemical signaling, providing a heritable basis for social discrimination in house mice.

Tactile and auditory senses

The house mouse (Mus musculus) possesses highly specialized tactile senses, primarily mediated by its mystacial vibrissae, a array of long, stiff arranged in rows on the . These vibrissae are embedded in deeply rooted follicles containing mechanoreceptors, such as rapidly adapting and slowly adapting types, that detect deflections caused by contact with objects during exploratory whisking behaviors. This sensory input enables precise object localization in three dimensions, allowing the mouse to map its immediate environment even in low-light conditions. Recent research has elucidated the innervation patterns of whisker follicles, revealing that Aδ-low threshold mechanoreceptive neurons form competitive receptive fields through homotypic interactions, ensuring targeted sensory coverage for fine tactile discrimination. In addition to vibrissae, the house mouse's guard hairs—coarse, longer body hairs—contribute to tactile sensing by detecting subtle air currents and vibrations through associated mechanoreceptors in the skin. These guard hairs, part of the pelage's stratified follicle types, transduce low-amplitude airflow displacements into neural signals, aiding in the detection of nearby disturbances or approaching threats without direct contact. This distributed tactile network complements the vibrissae, providing a broad-field sensitivity to environmental dynamics essential for in cluttered habitats. The of the house mouse is adapted for high-frequency sensitivity, with a spanning approximately 1 to 90 kHz, far exceeding that of humans and enabling detection of ultrasonic sounds inaudible to predators. The features a lightweight ossicular chain and a resonant bulla that optimize transmission of high frequencies, minimizing energy loss and enhancing sensitivity above 40 kHz through efficient to the . This structure supports the processing of brief, rapid acoustic cues critical for spatial awareness. House mice produce ultrasonic vocalizations in the 40-110 kHz range, which serve as a form of non-chemical communication, particularly in social contexts such as courtship, maternal care, territorial defense, and distress signaling. These vocalizations, often emitted during active exploration, facilitate interactions with conspecifics and convey emotional states. Auditory cues, including these ultrasounds, also play a role in social interactions, such as coordinating group activities.

Behavior

Daily activity patterns

House mice (Mus musculus) are primarily nocturnal or crepuscular, exhibiting heightened activity during the night with distinct peaks around dawn and under natural light-dark cycles. This pattern aligns with their aversion to bright light, allowing them to minimize predation risks while foraging in low-light conditions. In wild populations, activity levels increase throughout most of the night but sharply decline 3–4 hours before dawn, reflecting adaptations to diurnal predators. Their home range in typically spans approximately 3–10 m, particularly in high-density commensal populations where resources are abundant, though this can vary with environmental factors such as food availability and . In or semi-natural settings, observed ranges are often larger due to controlled environments with fewer constraints, sometimes exceeding 300 in experimental enclosures. These spatial patterns support efficient resource use within demes, or social units, where mice maintain territories for shelter and foraging. Foraging behavior is opportunistic and omnivorous, centered on seeds, grains, insects (such as beetle larvae, caterpillars, and cockroaches), and human food scraps in both urban and rural habitats. In commensal settings, particularly within wall voids and other structural cavities where mice commonly nest, they can sustain themselves on available insects when primary food sources are scarce, supplementing their diet with opportunistic protein and fat intake from such sources. Mice frequently cache excess food in secure, hidden sites such as burrows or structural voids to buffer against scarcity, a that enhances in fluctuating environments. In urban settings, they adapt by exploiting anthropogenic resources while displaying —a fear of novel objects or foods—that limits risky exploration and reduces exposure to traps or toxins. Recent studies highlight how artificial light disrupts these patterns, altering circadian rhythms in urban house mice. Exposure to constant or dim light at night suppresses nocturnal activity and desynchronizes clock , potentially leading to physiological stress and reduced foraging efficiency. A 2025 investigation using ultradian lighting cycles confirmed that such disruptions maintain some behavioral rhythms but impair overall entrainment to natural photoperiods.

Social structures

House mice form social groups known as demes, typically comprising 5-20 individuals centered around related females and their offspring, with one or more dominant males. These matrilineal structures arise from strong female , where approximately 77% of females preferentially breed within their natal group alongside their mothers, fostering cooperative affiliations among kin. Dominance hierarchies within these groups are sex-specific: males establish rank through aggressive interactions, such as fighting and chasing, to secure territorial control and access, while females maintain looser hierarchies based on affiliation and tolerance rather than overt . Subordinate males often face or reduced , whereas female kin bonds promote group stability and shared nursing of young. Territoriality is maintained through scent marking, primarily via urine deposits containing volatile proteins and pheromones, supplemented by secretions from sebaceous and preputial glands, which advertise dominance and deter intruders. Dominant males mark extensively to delineate boundaries, with marking rates increasing in response to rivals, thereby reducing intrusions and supporting hierarchical stability. Olfactory cues from these marks play a key role in territory establishment. Unrelated intruding males frequently commit against pups in established demes to eliminate competitors and accelerate the breeding cycle for their own offspring, a observed in 80-90% of unmated males but inhibited post-mating in sires. This tactic enhances the infanticidal male's reproductive fitness by prompting females to resume estrus sooner. Recent 2024 observations in semi-natural enclosures simulating high-density urban environments reveal flexible in house mice, with females driving denser, more dynamic networks that include temporary alliances for resource sharing and reduced isolation, adapting to fluctuating densities beyond rigid kin-based demes.

Reproduction and life history

Mating systems

House mice (Mus musculus) exhibit a promiscuous characterized by both males and females engaging with multiple partners during reproductive periods, driven by intense postcopulatory . Males compete primarily through , where the of multiple males vie for fertilization within the female's reproductive tract, a process facilitated by the ' hooked morphology that enhances competitive displacement. Female choice plays a complementary role, with females actively selecting mates based on traits such as dominance and genetic compatibility, often resulting in multiple paternity rates of 30-46% in wild litters. This multimale mating behavior promotes , allowing females to mate with several males, which can enhance in offspring by incorporating varied paternal contributions within litters. Polygyny is prevalent in house mouse social groups, where dominant territorial males typically monopolize access to multiple females within their demes, excluding subordinate males from breeding opportunities. These dominant males defend resources and mates aggressively, leading to hierarchical structures that favor high-ranking individuals in . However, females' polyandrous strategies counterbalance this by seeking copulations from non-dominant or novel males, potentially to avoid through mechanisms like mate preference for dissimilar genotypes. The evolutionary drivers of these mating systems yield mixed fitness outcomes. Multiple mating increases in litters, which may bolster offspring viability against environmental stressors, as evidenced by higher heterozygosity in multiply sired young. Yet, it also elevates the risk of , particularly when new dominant males enter groups and kill unrelated pups to accelerate female re-entry into estrus, though females may mitigate this via paternity confusion from .

Reproductive cycles

The reproductive cycle of the house mouse (Mus musculus) is characterized by a short lasting 4-6 days, during which females exhibit spontaneous but experience a reflex surge in triggered by pheromones, facilitating rapid fertilization. Following copulation, typically lasts 19-21 days, though it may extend slightly if the female is lactating from a previous . Litters average 5-6 pups but can range from 3-12, with females capable of producing up to 10 litters per year under optimal conditions, enabling high reproductive output. The promiscuous of house mice further supports this elevated by allowing multiple sires per litter. Pups are born altricial, hairless, deaf, and blind, weighing about 1 gram each. Postnatal development progresses rapidly: fur emerges by 2-4 days, ears open at 3-5 days, and eyes open at 12-14 days, marking the transition to increased mobility and sensory awareness. occurs around 21 days, when pups begin independent feeding, and is reached at 6-8 weeks, allowing females to breed soon after. In wild populations, breeding is influenced by environmental factors such as photoperiod, with peaking in spring and summer ( to ) under longer day lengths, though constant darkness or short photoperiods can suppress activity in some strains. Recent 2025 observations indicate that in resource-rich urban human habitats, warmer temperatures and abundant food supplies have accelerated , leading to year-round breeding cycles and increased litter frequencies compared to rural or seasonal wild settings.

Lifespan and aging

In the wild, house mice (Mus musculus) typically have a short lifespan, with a survival of about 130 days and 90% mortality occurring by approximately 280 days, though some individuals may survive up to 1-2 years under favorable conditions. In laboratory settings, where threats are minimized, their lifespan extends to an average of 2-3 years. The primary causes of mortality in wild populations include predation, infectious diseases, and , often exacerbated by environmental stressors such as harsh . Aging in house mice involves several physiological declines, including progressive telomere shortening, which contributes to and age-related pathologies like and organ dysfunction. accumulates with age due to imbalances in production and defenses, leading to macromolecular damage in tissues such as muscles and the . begins to decline after 6-12 months of age, with reduced oocyte quality and litter sizes reflecting broader reproductive . Recent interventions have demonstrated potential to modulate lifespan in laboratory house mice. Caloric restriction, implemented as a 40% reduction in intake, extends median lifespan by 20-50% across diverse strains, depending on the degree of restriction and genetic background, while also improving markers like immune function. Genetic models, such as the LmnaG609G/G609G , recapitulate human syndromes, exhibiting accelerated aging phenotypes including shortened lifespan, skeletal abnormalities, and premature death typically within 4-6 months. These models highlight the role of lamin A mutations in driving rapid aging processes.

Genetics

Genome structure

The house mouse (Mus musculus) spans approximately 2.7 billion base pairs, containing around 22,000 protein-coding genes. This compact structure facilitates extensive synteny with the , where about 90% of regions show conserved gene order despite rearrangements at breakpoints, enabling comparative genomic studies for identifying functional elements and disease-related loci. Chromosomally, the genome comprises 19 pairs of autosomes plus the X and Y, totaling 40 chromosomes in diploid cells. Key organizational features include four paralogous clusters (HoxA on , HoxB on 11, HoxC on 15, and HoxD on 2), which span roughly 100-200 kilobases each and encode transcription factors critical for embryonic patterning and . The initial draft of the house mouse reference genome, based on the C57BL/6J strain, was completed in 2002 through a collaborative effort that achieved over 90% coverage and highlighted mammalian evolutionary conservation. Subsequent assemblies in the 2010s, such as GRCm38 (2012) and GRCm39 (2020), refined contiguity and annotation, incorporating long-read sequencing to resolve repetitive regions. In 2025, high-quality chromosome-scale assemblies of subspecies like M. m. domesticus and M. m. musculus added over 200 megabases of novel sequence, including 500+ protein-coding genes, while GENCODE updates enhanced regulatory element identification for improved functional genomics.

Genetic diversity

House mice (Mus musculus) exhibit relatively high levels of genetic heterozygosity, attributable to their large effective sizes, estimated at around 10^5 individuals in wild populations, which maintain substantial diversity across the . This heterozygosity supports adaptive potential in commensal environments, with average expected heterozygosity values around 0.12 in Eurasian populations based on allozyme and analyses. The reference house mouse serves as a foundational tool for quantifying this variation through comparative sequencing. In hybrid zones where subspecies such as M. m. domesticus and M. m. musculus interbreed, admixture often leads to reduced , particularly on the , due to selective barriers and Dobzhansky-Muller incompatibilities that limit in hybrid genomes. Northern expansion fronts show even lower nucleotide diversity in admixed populations, reflecting ongoing hybridization dynamics and potential bottlenecks at contact edges. Prominent genetic variants in house mouse populations include the t-haplotype on chromosome 17, a selfish genetic element that causes transmission ratio distortion by favoring its own transmission to up to 99% of offspring through interactions between multiple distorter loci and a responder locus, despite reducing male fertility in homozygotes. This variant persists at frequencies of 10-30% in wild populations due to its meiotic drive advantage. Another key adaptation is the prevalence of warfarin resistance alleles in urban house mouse populations, primarily mutations in the Vkorc1 gene (e.g., Y139C and L128S variants) that confer resistance to anticoagulant rodenticides, with resistance documented in over 50% of sampled European urban populations exposed to human pest control. These alleles have spread rapidly in commensal settings, highlighting urban selection pressures. Recent genomic studies from 2023-2025, including genome-wide association analyses in wild-derived strains, have identified loci influencing behavioral traits such as anxiety and activity—proxies for —and immune responses to environmental stressors, revealing signatures of genetic bottlenecks associated with human . For instance, introductions to new continents like resulted in a severe bottleneck, reducing to 60% of European levels and fewer rare alleles, as inferred from whole-genome sequencing of invasive populations. Similarly, analyses of western European house mice confirm demographic contractions linked to historical human-mediated dispersal, with effective population sizes dropping during colonization events around 500-1500 years ago. These bottlenecks, driven by commensal reliance on human settlements, have shaped trait-associated variation, including potential adaptations to pathogens in altered habitats.

Human interactions

Historical and cultural roles

The house mouse (Mus musculus) has maintained a close commensal relationship with humans since the , with the earliest archaeological evidence originating from Natufian sites in the , such as Ain Mallaha in modern-day , dating to approximately 15,000 years ago. These remains indicate that house mice began exploiting settlements for food and shelter long before the full development of , marking the onset of their domestication-like adaptation to human environments. This association deepened with the around 12,000 years ago, as house mice co-evolved alongside early farming communities in the , thriving on stored grains and spreading via and trade routes across . Genetic and archaeological analyses of ancient remains confirm that house mice colonized human agricultural sites even prior to large-scale grain storage, highlighting their role in the ecological shifts accompanying sedentism. Recent studies, including those examining , further support this intertwined evolutionary history, showing adaptations in mouse populations that mirrored human agricultural expansion. Human dispersal facilitated the global spread of the house mouse, which reached the via European trade routes and ships following Christopher Columbus's voyages in 1492, establishing populations in the by the early 16th century. In cultural narratives, the house mouse often embodies cleverness and resourcefulness, as seen in from , where it appears as a trickster-like figure outwitting larger threats, such as in "The Lion and the Mouse" or "The Town Mouse and the Country Mouse." During the medieval era in , the house mouse symbolized devastation and impurity, frequently depicted in and literature as a harbinger of plague, particularly during the pandemics of the , where it represented disease transmission amid . In contrast, modern has reframed the house mouse positively through Walt Disney's , introduced in 1928, which evolved into a enduring icon of whimsy, resilience, and American optimism, influencing global entertainment and merchandise. With the rise of , this historical companionship transitioned into perceptions of the house mouse as a common household pest.

As pets and pests

House mice, particularly the domesticated fancy varieties, have been selectively bred as pets since the , with enthusiasts developing a wide array of coat colors, patterns, and even specific behavioral traits through careful genetic selection. These fancy mice, derived from the wild house mouse (Mus musculus), are prized for their docility and adaptability to captive life, making them popular companions in households worldwide. Proper care for pet mice emphasizes enriched environments to promote natural behaviors such as burrowing, climbing, and nesting. Cages should be spacious, secure, and multi-level, with at least 2 cm (0.8 inches) deep safe bedding material like paper-based substrates to allow and tunnel-building, alongside hiding spots, chew toys, and nesting materials to reduce stress and encourage activity. Habitats must be placed in quiet, draft-free areas away from direct , predators, and extreme temperatures, with daily spot-cleaning and full weekly changes to maintain . In contrast, wild house mice often become significant pests, infesting homes and causing damage through gnawing on structural materials, , and storage containers, which can lead to costly repairs and fire hazards. They contaminate food supplies and pantry items with , , and hair, rendering them unsafe for consumption and necessitating frequent disposal, while also spoiling non-food items like books and clothing. A single sighting of a house mouse in a human dwelling is uncommon as an isolated occurrence. Such sightings, particularly during the daytime when mice are primarily nocturnal, usually indicate the presence of additional mice—often several or many more. This is because house mice are social animals that live in groups or colonies, and females can produce multiple litters per year, enabling rapid population growth and leading to larger hidden populations in structures. Management of house mouse infestations typically involves integrated approaches prioritizing sanitation and exclusion, such as sealing entry points, removing food sources by storing pantry items in sealed containers, cleaning up crumbs, and taking out trash regularly, as well as reducing access to water by fixing leaks. After trapping or population reduction, thoroughly clean droppings, urine, and nests by first spraying with a disinfectant or bleach solution and wearing protective gear including gloves and a mask to safely remove waste and eliminate scent trails and attractants that could draw more mice. This is followed by population reduction using traps or rodenticides. Snap traps and glue boards are effective for small infestations, placed along walls and runways where mice travel, offering a non-toxic option safer around children and pets compared to chemical baits. For larger problems, second-generation anticoagulant rodenticides like brodifacoum are used in tamper-resistant bait stations to prevent secondary poisoning, though they require careful placement to minimize risks to non-target wildlife. The economic toll of house mouse pests is substantial, with global costs from invasive rodents—including house mice—totaling over $3.6 billion from 1930 to 2022, with annual costs averaging $38.7 million between 1980 and 2022, encompassing direct damage to , structures, and stored , as well as control expenses. In 2025, innovations in eco-friendly traps, such as the Goodnature self-resetting humane trap, have gained recognition for their toxin-free, reusable design that dispatches mice instantly and alerts users via app, reducing environmental impact while effectively managing infestations.

Disease vectors and invasive impacts

House mice (Mus musculus) are generally not as unhealthy or dangerous to human health as rats, though both can serve as vectors for zoonotic diseases through contamination of environments with urine, feces, droppings, or saliva, as well as via bites in rare cases. Both house mice and rats can transmit salmonellosis through fecal contamination of food and surfaces. However, rats pose greater health risks due to their larger size (producing greater volumes of urine and feces), more aggressive behavior (higher likelihood of biting), and stronger association with severe diseases such as leptospirosis, rat-bite fever, and plague. House mice are more specifically linked to lymphocytic choriomeningitis virus (LCMV) and are less commonly associated with hantavirus, which is primarily carried by deer mice. Overall, while both rodents are hazardous and should be controlled, rats are considered more dangerous to human health. Hantavirus, which can cause hantavirus pulmonary syndrome in humans, is transmitted mainly through inhalation of aerosolized particles from infected rodent excreta or nesting materials, but is primarily associated with deer mice rather than house mice. Salmonellosis, a bacterial infection leading to gastroenteritis, spreads when humans ingest food or water contaminated by mouse feces containing Salmonella bacteria. Lymphocytic choriomeningitis virus (LCMV), which can result in flu-like symptoms or more severe neurological complications, is primarily carried by house mice and transmitted through exposure to their urine, droppings, saliva, or direct contact via bites or scratches. As , house mice have profound ecological impacts, particularly on islands where they lack natural predators and outcompete native for resources, leading to declines in endemic populations. In , house mice dominate in predator-free areas such as islands and fenced sanctuaries, suppressing native small mammals and through competition and predation. Their disrupts vegetation regeneration; for instance, mice consume seeds of native plants like kauri () and pingao (Desmoschoenus spiralis), altering forest and coastal ecosystems. On in the South Atlantic, house mice prey on chicks and even adults, prompting large-scale eradication efforts in the 2020s, including a major operation in 2021 that, despite extensive baiting, ultimately failed due to incomplete coverage and logistical challenges like invasive slugs interfering with bait distribution. Recent surveillance efforts have highlighted house mice's role in harboring antibiotic-resistant in urban settings, posing risks to . A 2025 study on wild , including house mice, found high prevalence of antimicrobial-resistant pathogens such as extended-spectrum beta-lactamase-producing in urban and peri-urban populations, attributing this to their proximity to and antibiotic-polluted environments. These findings underscore the need for integrated monitoring of rodent reservoirs to track the spread of resistance genes in densely populated areas.

Use as model organisms

The house mouse (Mus musculus) serves as a in biomedical due to its genetic similarity to humans, short generation time, and ease of manipulation, enabling precise modeling of physiological and pathological processes. Inbred strains, such as , have been developed through over 200 generations of brother-sister mating to achieve genetic uniformity, minimizing variability in experimental outcomes and facilitating reproducible results across studies. This strain, often referred to as "Black 6," is the most widely used in the world for its robust health, well-characterized , and suitability for long-term experiments. Genetic engineering techniques have further enhanced the utility of house mice as model organisms, particularly through models that disrupt specific to elucidate their functions. Since 2013, CRISPR/Cas9 technology has revolutionized this process by enabling rapid, efficient creation of targeted mutations, allowing researchers to generate knockouts and knock-ins with high precision and reduced off-target effects compared to earlier methods like . These models are instrumental in studying roles in development, , and , with applications spanning from to therapeutic development. House mice are extensively employed in modeling complex diseases, including , , and , where their and neural architecture closely parallel human counterparts. In , syngeneic tumor models using immunocompetent mice like help evaluate immunotherapies and tumor-immune interactions, providing insights into checkpoint inhibitors and adoptive cell therapies. studies leverage mouse models to investigate , neurodegeneration, and behavioral disorders, often using in knockouts to map neural circuits. In , models—engrafted with human hematopoietic stem cells and immune components—simulate human immune responses, aiding development and infectious disease . These applications have contributed to numerous breakthroughs, with animal models, including mice, involved in over 80% of s in Physiology or Medicine since 1901, underscoring their pivotal role in advancing human health. For instance, the 2025 in Physiology or Medicine, awarded for discoveries on regulatory T cells and the in , utilized mouse models to identify key mechanisms of prevention. Recent ethical advancements emphasize the 3Rs principles (replacement, reduction, refinement) to minimize use, with 2024 guidelines from regulatory bodies promoting alternatives like organoids—three-dimensional cell cultures derived from stem cells that mimic organ structures—for preliminary and testing. These organoids reduce the number of mice needed in screening by providing human-relevant data without whole- experimentation. Concurrently, models continue to evolve for transplant research, incorporating patient-specific immune cells to predict graft rejection and optimize donor matching, balancing scientific necessity with welfare considerations. The genetic tractability of house mice, including their sequenced and ease of transgenesis, underpins these modeling capabilities, allowing targeted perturbations that mirror human genetic variations.

References

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