pre-piRNA trimming and 2′-O-methylation protect piRNAs from 3′ tailing and degradation in C. elegans

被引:25
|
作者
Pastore, Benjamin [1 ,2 ,3 ]
Hertz, Hannah L. [1 ,2 ]
Price, Ian F. [1 ,2 ,3 ]
Tang, Wen [1 ,2 ]
机构
[1] Dept Biol Chem & Pharmacol, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr RNA Biol, Columbus, OH 43210 USA
[3] Ohio State Biochem Program, Columbus, OH 43210 USA
来源
CELL REPORTS | 2021年 / 36卷 / 09期
关键词
PIWI-INTERACTING RNAS; EPIGENETIC MEMORY; BIOGENESIS; GERMLINE; ZUCCHINI; MICRORNAS; REVEALS; IDENTIFICATION; POLYMERASE; 21U-RNAS;
D O I
10.1016/j.celrep.2021.109640
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Piwi-interacting RNA (piRNA) pathway suppresses transposable elements and promotes fertility in diverse organisms. Maturation of piRNAs involves pre-piRNA trimming followed by 2'-O-methylation at their 30 termini. Here, we report that the 3' termini of Caenorhabditis elegans piRNAs are subject to nontemplated nucleotide addition, and piRNAs with 3' addition exhibit extensive base-pairing interaction with their target RNAs. Animals deficient for PARN-1 (pre-piRNA trimmer) and HENN-1 (2'-O-methyltransferase) accumulate piRNAs with 3' nontemplated nucleotides. In henn-1 mutants, piRNAs are shortened prior to 3' addition, whereas long isoforms of untrimmed piRNAs are preferentially modified in parn-1 mutant animals. Loss of either PARN-1 or HENN-1 results in modest reduction in steady-state levels of piRNAs. Deletion of both enzymes leads to depletion of piRNAs, desilenced piRNA targets, and impaired fecundity. Together, our findings suggest that pre-piRNA trimming and 2'-O-methylation act collaboratively to protect piRNAs from tailing and degradation.
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页数:19
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