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Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori

Sex determination pathways are astoundingly diverse in insects. For instance, the silk moth Bombyx mori uniquely use various components of the piRNA pathway to produce the Fem signal for specification of the female fate. In this study, we identified BmGTSF1 as a novel piRNA factor which participates...

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Autores principales: Chen, Kai, Yu, Ye, Yang, Dehong, Yang, Xu, Tang, Linmeng, Liu, Yujia, Luo, Xingyu, R. Walter, James, Liu, Zulian, Xu, Jun, Huang, Yongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660909/
https://www.ncbi.nlm.nih.gov/pubmed/33137136
http://dx.doi.org/10.1371/journal.pgen.1009194
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author Chen, Kai
Yu, Ye
Yang, Dehong
Yang, Xu
Tang, Linmeng
Liu, Yujia
Luo, Xingyu
R. Walter, James
Liu, Zulian
Xu, Jun
Huang, Yongping
author_facet Chen, Kai
Yu, Ye
Yang, Dehong
Yang, Xu
Tang, Linmeng
Liu, Yujia
Luo, Xingyu
R. Walter, James
Liu, Zulian
Xu, Jun
Huang, Yongping
author_sort Chen, Kai
collection PubMed
description Sex determination pathways are astoundingly diverse in insects. For instance, the silk moth Bombyx mori uniquely use various components of the piRNA pathway to produce the Fem signal for specification of the female fate. In this study, we identified BmGTSF1 as a novel piRNA factor which participates in B. mori sex determination. We found that BmGtsf1 has a distinct expression pattern compared to Drosophila and mouse. CRISPR/Cas9 induced mutation in BmGtsf1 resulted in partial sex reversal in genotypically female animals by shifting expression of the downstream targets BmMasc and Bmdsx to the male pattern. As levels of Fem piRNAs were substantially reduced in female mutants, we concluded that BmGtsf1 plays a critical role in the biogenesis of the feminizing signal. We also demonstrated that BmGTSF1 physically interacted with BmSIWI, a protein previously reported to be involved in female sex determination, indicating BmGTSF1 function as the cofactor of BmSIWI. BmGtsf1 mutation resulted in piRNA pathway dysregulation, including piRNA biogenesis defects and transposon derepression, suggesting BmGtsf1 is also a piRNA factor in the silkworm. Furthermore, we found that BmGtsf1 mutation leads to gametogenesis defects in both male and female. Our data suggested that BmGtsf1 is a new component involved in the sex determination pathway in B. mori.
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spelling pubmed-76609092020-11-18 Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori Chen, Kai Yu, Ye Yang, Dehong Yang, Xu Tang, Linmeng Liu, Yujia Luo, Xingyu R. Walter, James Liu, Zulian Xu, Jun Huang, Yongping PLoS Genet Research Article Sex determination pathways are astoundingly diverse in insects. For instance, the silk moth Bombyx mori uniquely use various components of the piRNA pathway to produce the Fem signal for specification of the female fate. In this study, we identified BmGTSF1 as a novel piRNA factor which participates in B. mori sex determination. We found that BmGtsf1 has a distinct expression pattern compared to Drosophila and mouse. CRISPR/Cas9 induced mutation in BmGtsf1 resulted in partial sex reversal in genotypically female animals by shifting expression of the downstream targets BmMasc and Bmdsx to the male pattern. As levels of Fem piRNAs were substantially reduced in female mutants, we concluded that BmGtsf1 plays a critical role in the biogenesis of the feminizing signal. We also demonstrated that BmGTSF1 physically interacted with BmSIWI, a protein previously reported to be involved in female sex determination, indicating BmGTSF1 function as the cofactor of BmSIWI. BmGtsf1 mutation resulted in piRNA pathway dysregulation, including piRNA biogenesis defects and transposon derepression, suggesting BmGtsf1 is also a piRNA factor in the silkworm. Furthermore, we found that BmGtsf1 mutation leads to gametogenesis defects in both male and female. Our data suggested that BmGtsf1 is a new component involved in the sex determination pathway in B. mori. Public Library of Science 2020-11-02 /pmc/articles/PMC7660909/ /pubmed/33137136 http://dx.doi.org/10.1371/journal.pgen.1009194 Text en © 2020 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chen, Kai
Yu, Ye
Yang, Dehong
Yang, Xu
Tang, Linmeng
Liu, Yujia
Luo, Xingyu
R. Walter, James
Liu, Zulian
Xu, Jun
Huang, Yongping
Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori
title Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori
title_full Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori
title_fullStr Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori
title_full_unstemmed Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori
title_short Gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, Bombyx mori
title_sort gtsf1 is essential for proper female sex determination and transposon silencing in the silkworm, bombyx mori
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660909/
https://www.ncbi.nlm.nih.gov/pubmed/33137136
http://dx.doi.org/10.1371/journal.pgen.1009194
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