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EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis
EXOSC10 is a catalytic subunit of the exosome that processes biologically active transcripts, degrades aberrant mRNAs and targets certain long non-coding RNAs (lncRNAs). The yeast orthologue Rrp6 is required for efficient growth and gametogenesis, and becomes unstable during meiosis. However, nothin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678167/ https://www.ncbi.nlm.nih.gov/pubmed/29118343 http://dx.doi.org/10.1038/s41598-017-14643-y |
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author | Jamin, Soazik P. Petit, Fabrice G. Kervarrec, Christine Smagulova, Fatima Illner, Doris Scherthan, Harry Primig, Michael |
author_facet | Jamin, Soazik P. Petit, Fabrice G. Kervarrec, Christine Smagulova, Fatima Illner, Doris Scherthan, Harry Primig, Michael |
author_sort | Jamin, Soazik P. |
collection | PubMed |
description | EXOSC10 is a catalytic subunit of the exosome that processes biologically active transcripts, degrades aberrant mRNAs and targets certain long non-coding RNAs (lncRNAs). The yeast orthologue Rrp6 is required for efficient growth and gametogenesis, and becomes unstable during meiosis. However, nothing is known about the localization, stability and function of EXOSC10 in the rodent male germline. We detect the protein in nucleoli and the cytoplasm of mitotic and meiotic germ cells, and find that it transiently associates with the XY body, a structure targeted by meiotic sex chromosome inactivation (MSCI). Finally, EXOSC10 becomes unstable at later stages of gamete development. To determine Exosc10’s meiotic function, we inactivated the gene specifically in male germ cells using cre recombinase controlled by Stra8 or Ddx4/Vasa promoters. Mutant mice have small testes, show impaired germ cell differentiation and are subfertile. Our results demonstrate that EXOSC10 is post-translationally regulated in germ cells, associate the protein with epigenetic chromosome silencing, and reveal its essential role in germ cell growth and development. |
format | Online Article Text |
id | pubmed-5678167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56781672017-11-17 EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis Jamin, Soazik P. Petit, Fabrice G. Kervarrec, Christine Smagulova, Fatima Illner, Doris Scherthan, Harry Primig, Michael Sci Rep Article EXOSC10 is a catalytic subunit of the exosome that processes biologically active transcripts, degrades aberrant mRNAs and targets certain long non-coding RNAs (lncRNAs). The yeast orthologue Rrp6 is required for efficient growth and gametogenesis, and becomes unstable during meiosis. However, nothing is known about the localization, stability and function of EXOSC10 in the rodent male germline. We detect the protein in nucleoli and the cytoplasm of mitotic and meiotic germ cells, and find that it transiently associates with the XY body, a structure targeted by meiotic sex chromosome inactivation (MSCI). Finally, EXOSC10 becomes unstable at later stages of gamete development. To determine Exosc10’s meiotic function, we inactivated the gene specifically in male germ cells using cre recombinase controlled by Stra8 or Ddx4/Vasa promoters. Mutant mice have small testes, show impaired germ cell differentiation and are subfertile. Our results demonstrate that EXOSC10 is post-translationally regulated in germ cells, associate the protein with epigenetic chromosome silencing, and reveal its essential role in germ cell growth and development. Nature Publishing Group UK 2017-11-08 /pmc/articles/PMC5678167/ /pubmed/29118343 http://dx.doi.org/10.1038/s41598-017-14643-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jamin, Soazik P. Petit, Fabrice G. Kervarrec, Christine Smagulova, Fatima Illner, Doris Scherthan, Harry Primig, Michael EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis |
title | EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis |
title_full | EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis |
title_fullStr | EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis |
title_full_unstemmed | EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis |
title_short | EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis |
title_sort | exosc10/rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678167/ https://www.ncbi.nlm.nih.gov/pubmed/29118343 http://dx.doi.org/10.1038/s41598-017-14643-y |
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