 | This article may be confusing or unclear to readers. (August 2016) |
isomiRs (from iso- + miR) are miRNA sequences that have variations with respect to the reference sequence. The term was coined by Morin et al in 2008.[1] It has been found that isomiR expression profiles can also exhibit race, population, and sex dependencies.[2]
There are four main variation types:
miRBase is considered to be the gold-standard miRNA database—it stores miRNA sequences detected by thousand of experiments. In this database each miRNA is associated with a miRNA precursor and with one or two mature miRNA (-5p and -3p). In the past it had always been said that the same miRNA precursor generates the same miRNA sequences. However, the advent of deep sequencing has now allowed researchers to detect a huge variability in miRNA biogenesis, meaning that from the same miRNA precursor many different sequences can be generated potentially have different targets,[3][4][5] or even lead to opposite changes in mRNA expression.[4]
The advent of sequencing has permitted scientists to elucidate a huge landscape of new miRNAs, to increase our knowledge of the biogenesis involved and to discover putative post-transcriptional editing processes in miRNAs ignored until now. These processes mostly generate variations of the current miRNAs that are annotated in miRBase in the 3' and 5' terminus and in minor frequencies, nucleotide substitution along the miRNA length.[6][7][8][9] The variations are mainly generated by a shift of Drosha and Dicer in the cleavage site, but also by nucleotide additions at the 3'-end,[10] resulting in new sequences different from the annotated miRNA. These were named "isomiRs" by Morin et al., 2008. IsomiRs have been well established along different species in metazoa[11][12][13][14][15] and deeply described for the first time in human stem cells and human brain samples.[8][9] Moreover, it has been proven that isomiRs are not caused by RNA degradation during sample preparation for next generation sequencing.[16] Some studies have tried to explain the miRNA diversity by structural bases of precursors but without clear results.[17] The functionality of adenylation or uridynilation at the 3'end (3'addition isomiRs) has been related to alterations in the miRNA-3'-UTR stability.[18] Furthermore, differential expression of isomiRs has been detected during development in D. melanogaster and Hippoglossus hippoglossus L., suggesting a biological function.[15][19]
