| Literature DB >> 33587037 |
Charlotte P Choi1, Rebecca J Tay1, Margaret R Starostik1, Suhua Feng2,3, James J Moresco4, Brooke E Montgomery5, Emily Xu1, Maya A Hammonds1, Michael C Schatz1,6, Taiowa A Montgomery5, John R Yates7, Steven E Jacobsen2,8, John K Kim1.
Abstract
Piwi-interacting RNAs (piRNAs) play essential roles in silencing repetitive elements to promote fertility in metazoans. Studies in worms, flies, and mammals reveal that piRNAs are expressed in a sex-specific manner. However, the mechanisms underlying this sex-specific regulation are unknown. Here we identify SNPC-1.3, a male germline-enriched variant of a conserved subunit of the small nuclear RNA-activating protein complex, as a male-specific piRNA transcription factor in Caenorhabditis elegans. SNPC-1.3 colocalizes with the core piRNA transcription factor, SNPC-4, in nuclear foci of the male germline. Binding of SNPC-1.3 at male piRNA loci drives spermatogenic piRNA transcription and requires SNPC-4. Loss of snpc-1.3 leads to depletion of male piRNAs and defects in male-dependent fertility. Furthermore, TRA-1, a master regulator of sex determination, binds to the snpc-1.3 promoter and represses its expression during oogenesis. Loss of TRA-1 targeting causes ectopic expression of snpc-1.3 and male piRNAs during oogenesis. Thus, sexually dimorphic regulation of snpc-1.3 expression coordinates male and female piRNA expression during germline development.Entities:
Keywords: C. elegans; TRA-1; chromosomes; gene expression; genetics; genomics; germline development; piRNA; sex determination; spermatogenesis; transcription
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Year: 2021 PMID: 33587037 PMCID: PMC7884074 DOI: 10.7554/eLife.60681
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.713