RT Journal Article
SR Electronic
T1 Interplay of target site architecture and miRNA abundance determine miRNA activity and specificity
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 214817
DO 10.1101/214817
A1 Giovanna Brancati
A1 Sarah H. Carl
A1 Helge Großhans
YR 2017
UL http://biorxiv.org/content/early/2017/11/21/214817.abstract
AB The recognition that the miRNA seed sequence is a major determinant of miRNA activity has greatly advanced the ability to predict miRNA targets. However, it has remained unclear to what extent miRNAs act redundantly when they are members of the same family and thus share a common seed. Using in vivo studies in C. elegans, we uncover features that drive specific target repression by individual miRNA family members. We find that seed-distal complementarity to a specific family member promotes specificity. However, the extent and robustness of specificity are greatly increased by seed match ‘imperfections’, such as bulges and G:U wobble base pairs. Depending on the seed match architecture, specificity may be overcome by increasing the levels of a miRNA lacking seed-distal complementarity. Hence, in contrast to a binary distinction between functional and non-functional target sites, our data support a model where functionality depends on a combination of target site quality and miRNA abundance. This emphasizes the importance of studying miRNAs under physiological conditions in their endogenous contexts.