SNPC-1.3 is a sex-specific transcription factor that drives male piRNA expression in C. elegans

Author:

Choi Charlotte P1ORCID,Tay Rebecca J1ORCID,Starostik Margaret R1ORCID,Feng Suhua23,Moresco James J4,Montgomery Brooke E5,Xu Emily1,Hammonds Maya A1,Schatz Michael C16,Montgomery Taiowa A5ORCID,Yates John R7ORCID,Jacobsen Steven E28,Kim John K1ORCID

Affiliation:

1. Department of Biology, Johns Hopkins University, Baltimore, United States

2. Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, United States

3. Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California, Los Angeles, Los Angeles, United States

4. Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, United States

5. Department of Biology, Colorado State University, Fort Collins, United States

6. Department of Computer Science, Johns Hopkins University, Baltimore, United States

7. Department of Molecular Medicine, The Scripps Research Institute, La Jolla, United States

8. Howard Hughes Medical Institute, University of California, Los Angeles, Los Angeles, United States

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 inCaenorhabditis 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 ofsnpc-1.3leads to depletion of male piRNAs and defects in male-dependent fertility. Furthermore, TRA-1, a master regulator of sex determination, binds to thesnpc-1.3promoter and represses its expression during oogenesis. Loss of TRA-1 targeting causes ectopic expression ofsnpc-1.3and male piRNAs during oogenesis. Thus, sexually dimorphic regulation ofsnpc-1.3expression coordinates male and female piRNA expression during germline development.

Funder

National Science Foundation

National Institute of General Medical Sciences

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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