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piRNA-mediated gene regulation and adaptation to sex-specific transposon expression in D. melanogaster male germline

Small noncoding piRNAs act as sequence-specific guides to repress complementary targets in Metazoa. Prior studies in Drosophila ovaries have demonstrated the function of the piRNA pathway in transposon silencing and therefore genome defense. However, the ability of the piRNA program to respond to di...

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Autores principales: Chen, Peiwei, Kotov, Alexei A., Godneeva, Baira K., Bazylev, Sergei S., Olenina, Ludmila V., Aravin, Alexei A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168559/
https://www.ncbi.nlm.nih.gov/pubmed/33985970
http://dx.doi.org/10.1101/gad.345041.120
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author Chen, Peiwei
Kotov, Alexei A.
Godneeva, Baira K.
Bazylev, Sergei S.
Olenina, Ludmila V.
Aravin, Alexei A.
author_facet Chen, Peiwei
Kotov, Alexei A.
Godneeva, Baira K.
Bazylev, Sergei S.
Olenina, Ludmila V.
Aravin, Alexei A.
author_sort Chen, Peiwei
collection PubMed
description Small noncoding piRNAs act as sequence-specific guides to repress complementary targets in Metazoa. Prior studies in Drosophila ovaries have demonstrated the function of the piRNA pathway in transposon silencing and therefore genome defense. However, the ability of the piRNA program to respond to different transposon landscapes and the role of piRNAs in regulating host gene expression remain poorly understood. Here, we comprehensively analyzed piRNA expression and defined the repertoire of their targets in Drosophila melanogaster testes. Comparison of piRNA programs between sexes revealed sexual dimorphism in piRNA programs that parallel sex-specific transposon expression. Using a novel bioinformatic pipeline, we identified new piRNA clusters and established complex satellites as dual-strand piRNA clusters. While sharing most piRNA clusters, the two sexes employ them differentially to combat the sex-specific transposon landscape. We found two piRNA clusters that produce piRNAs antisense to four host genes in testis, including CG12717/pirate, a SUMO protease gene. piRNAs encoded on the Y chromosome silence pirate, but not its paralog, to exert sex- and paralog-specific gene regulation. Interestingly, pirate is targeted by endogenous siRNAs in a sibling species, Drosophila mauritiana, suggesting distinct but related silencing strategies invented in recent evolution to regulate a conserved protein-coding gene.
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spelling pubmed-81685592021-12-01 piRNA-mediated gene regulation and adaptation to sex-specific transposon expression in D. melanogaster male germline Chen, Peiwei Kotov, Alexei A. Godneeva, Baira K. Bazylev, Sergei S. Olenina, Ludmila V. Aravin, Alexei A. Genes Dev Research Paper Small noncoding piRNAs act as sequence-specific guides to repress complementary targets in Metazoa. Prior studies in Drosophila ovaries have demonstrated the function of the piRNA pathway in transposon silencing and therefore genome defense. However, the ability of the piRNA program to respond to different transposon landscapes and the role of piRNAs in regulating host gene expression remain poorly understood. Here, we comprehensively analyzed piRNA expression and defined the repertoire of their targets in Drosophila melanogaster testes. Comparison of piRNA programs between sexes revealed sexual dimorphism in piRNA programs that parallel sex-specific transposon expression. Using a novel bioinformatic pipeline, we identified new piRNA clusters and established complex satellites as dual-strand piRNA clusters. While sharing most piRNA clusters, the two sexes employ them differentially to combat the sex-specific transposon landscape. We found two piRNA clusters that produce piRNAs antisense to four host genes in testis, including CG12717/pirate, a SUMO protease gene. piRNAs encoded on the Y chromosome silence pirate, but not its paralog, to exert sex- and paralog-specific gene regulation. Interestingly, pirate is targeted by endogenous siRNAs in a sibling species, Drosophila mauritiana, suggesting distinct but related silencing strategies invented in recent evolution to regulate a conserved protein-coding gene. Cold Spring Harbor Laboratory Press 2021-06 /pmc/articles/PMC8168559/ /pubmed/33985970 http://dx.doi.org/10.1101/gad.345041.120 Text en © 2021 Chen et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research Paper
Chen, Peiwei
Kotov, Alexei A.
Godneeva, Baira K.
Bazylev, Sergei S.
Olenina, Ludmila V.
Aravin, Alexei A.
piRNA-mediated gene regulation and adaptation to sex-specific transposon expression in D. melanogaster male germline
title piRNA-mediated gene regulation and adaptation to sex-specific transposon expression in D. melanogaster male germline
title_full piRNA-mediated gene regulation and adaptation to sex-specific transposon expression in D. melanogaster male germline
title_fullStr piRNA-mediated gene regulation and adaptation to sex-specific transposon expression in D. melanogaster male germline
title_full_unstemmed piRNA-mediated gene regulation and adaptation to sex-specific transposon expression in D. melanogaster male germline
title_short piRNA-mediated gene regulation and adaptation to sex-specific transposon expression in D. melanogaster male germline
title_sort pirna-mediated gene regulation and adaptation to sex-specific transposon expression in d. melanogaster male germline
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168559/
https://www.ncbi.nlm.nih.gov/pubmed/33985970
http://dx.doi.org/10.1101/gad.345041.120
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