| Literature DB >> 24699545 |
Priscilla M Van Wynsberghe1, Emily F Finnegan2, Thomas Stark3, Evan P Angelus4, Kathryn E Homan4, Gene W Yeo5, Amy E Pasquinelli6.
Abstract
MicroRNAs (miRNAs) are small RNAs that post-transcriptionally regulate gene expression in many multicellular organisms. They are encoded in the genome and transcribed into primary (pri-) miRNAs before two processing steps that ultimately produce the mature miRNA. In order to generate the appropriate amount of a particular miRNA in the correct location at the correct time, proper regulation of miRNA biogenesis is essential. Here we identify the Period protein homolog LIN-42 as a new regulator of miRNA biogenesis in Caenorhabditis elegans. We mapped a spontaneous suppressor of the normally lethal let-7(n2853) allele to the lin-42 gene. Mutations in this allele (ap201) or a second lin-42 allele (n1089) caused increased mature let-7 miRNA levels at most time points when mature let-7 miRNA is normally expressed. Levels of pri-let-7 and a let-7 transcriptional reporter were also increased in lin-42(n1089) worms. These results indicate that LIN-42 normally represses pri-let-7 transcription and thus the accumulation of let-7 miRNA. This inhibition is not specific to let-7, as pri- and mature levels of lin-4 and miR-35 were also increased in lin-42 mutants. Furthermore, small RNA-seq analysis showed widespread increases in the levels of mature miRNAs in lin-42 mutants. Thus, we propose that the period protein homolog LIN-42 is a global regulator of miRNA biogenesis.Entities:
Keywords: C. elegans; Let-7; Lin-42; MicroRNA; Period
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Year: 2014 PMID: 24699545 PMCID: PMC4077587 DOI: 10.1016/j.ydbio.2014.03.017
Source DB: PubMed Journal: Dev Biol ISSN: 0012-1606 Impact factor: 3.582