| Literature DB >> 26919432 |
Wen Tang1, Shikui Tu2, Heng-Chi Lee1, Zhiping Weng2, Craig C Mello3.
Abstract
Piwi-interacting RNAs (piRNAs) engage Piwi proteins to suppress transposons and are essential for fertility in diverse organisms. An interesting feature of piRNAs is that, while piRNA lengths are stereotypical within a species, they can differ widely between species. For example, piRNAs are mainly 29 and 30 nucleotides in humans, 24 to 30 nucleotides in D. melanogaster, and uniformly 21 nucleotides in C. elegans. However, how piRNA length is determined and whether length impacts function remains unknown. Here, we show that C. elegans deficient for PARN-1, a conserved RNase, accumulate untrimmed piRNAs with 3' extensions. Surprisingly, these longer piRNAs are stable and associate with the Piwi protein PRG-1 but fail to robustly recruit downstream silencing factors. Our findings identify PARN-1 as a key regulator of piRNA length in C. elegans and suggest that length is regulated to promote efficient transcriptome surveillance.Entities:
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Year: 2016 PMID: 26919432 PMCID: PMC4785802 DOI: 10.1016/j.cell.2016.02.008
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582