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IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene
Meiosis initiation and progression are regulated by both germ cells and gonadal somatic cells. However, little is known about what genes or proteins connecting somatic and germ cells are required for this regulation. Our results show that deficiency for adhesion molecule IGSF11, which is expressed i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448346/ https://www.ncbi.nlm.nih.gov/pubmed/34491997 http://dx.doi.org/10.1371/journal.pgen.1009778 |
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author | Chen, Bo Zhu, Gengzhen Yan, An He, Jing Liu, Yang Li, Lin Yang, Xuerui Dong, Chen Kee, Kehkooi |
author_facet | Chen, Bo Zhu, Gengzhen Yan, An He, Jing Liu, Yang Li, Lin Yang, Xuerui Dong, Chen Kee, Kehkooi |
author_sort | Chen, Bo |
collection | PubMed |
description | Meiosis initiation and progression are regulated by both germ cells and gonadal somatic cells. However, little is known about what genes or proteins connecting somatic and germ cells are required for this regulation. Our results show that deficiency for adhesion molecule IGSF11, which is expressed in both Sertoli cells and germ cells, leads to male infertility in mice. Combining a new meiotic fluorescent reporter system with testicular cell transplantation, we demonstrated that IGSF11 is required in both somatic cells and spermatogenic cells for primary spermatocyte development. In the absence of IGSF11, spermatocytes proceed through pachytene, but the pericentric heterochromatin of nonhomologous chromosomes remains inappropriately clustered from late pachytene onward, resulting in undissolved interchromosomal interactions. Hi-C analysis reveals elevated levels of interchromosomal interactions occurring mostly at the chromosome ends. Collectively, our data elucidates that IGSF11 in somatic cells and germ cells is required for pericentric heterochromatin dissociation during diplotene in mouse primary spermatocytes. |
format | Online Article Text |
id | pubmed-8448346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84483462021-09-18 IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene Chen, Bo Zhu, Gengzhen Yan, An He, Jing Liu, Yang Li, Lin Yang, Xuerui Dong, Chen Kee, Kehkooi PLoS Genet Research Article Meiosis initiation and progression are regulated by both germ cells and gonadal somatic cells. However, little is known about what genes or proteins connecting somatic and germ cells are required for this regulation. Our results show that deficiency for adhesion molecule IGSF11, which is expressed in both Sertoli cells and germ cells, leads to male infertility in mice. Combining a new meiotic fluorescent reporter system with testicular cell transplantation, we demonstrated that IGSF11 is required in both somatic cells and spermatogenic cells for primary spermatocyte development. In the absence of IGSF11, spermatocytes proceed through pachytene, but the pericentric heterochromatin of nonhomologous chromosomes remains inappropriately clustered from late pachytene onward, resulting in undissolved interchromosomal interactions. Hi-C analysis reveals elevated levels of interchromosomal interactions occurring mostly at the chromosome ends. Collectively, our data elucidates that IGSF11 in somatic cells and germ cells is required for pericentric heterochromatin dissociation during diplotene in mouse primary spermatocytes. Public Library of Science 2021-09-07 /pmc/articles/PMC8448346/ /pubmed/34491997 http://dx.doi.org/10.1371/journal.pgen.1009778 Text en © 2021 Chen et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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, Bo Zhu, Gengzhen Yan, An He, Jing Liu, Yang Li, Lin Yang, Xuerui Dong, Chen Kee, Kehkooi IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene |
title | IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene |
title_full | IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene |
title_fullStr | IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene |
title_full_unstemmed | IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene |
title_short | IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene |
title_sort | igsf11 is required for pericentric heterochromatin dissociation during meiotic diplotene |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448346/ https://www.ncbi.nlm.nih.gov/pubmed/34491997 http://dx.doi.org/10.1371/journal.pgen.1009778 |
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