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Dnajb8, a target gene of SOX30, is dispensable for male fertility in mice
BACKGROUND: The DNAJ family of molecular chaperones maintains protein homeostasis in mitotic and postmeiotic cells, especially germ cells. Recently, we found that the transcription factor SOX30 initiates transcription of Dnajb8 during late meiosis and spermiogenesis in mouse testes. METHODS: We used...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759119/ https://www.ncbi.nlm.nih.gov/pubmed/33391882 http://dx.doi.org/10.7717/peerj.10582 |
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author | Wang, Fengsong Kong, Shuai Hu, Xuechun Li, Xin Xu, Bo Yue, Qiuling Fu, Kaiqiang Ye, Lan Bai, Shun |
author_facet | Wang, Fengsong Kong, Shuai Hu, Xuechun Li, Xin Xu, Bo Yue, Qiuling Fu, Kaiqiang Ye, Lan Bai, Shun |
author_sort | Wang, Fengsong |
collection | PubMed |
description | BACKGROUND: The DNAJ family of molecular chaperones maintains protein homeostasis in mitotic and postmeiotic cells, especially germ cells. Recently, we found that the transcription factor SOX30 initiates transcription of Dnajb8 during late meiosis and spermiogenesis in mouse testes. METHODS: We used the CRISPR/Cas9 system to generate Dnajb8 mutant mice and analyze the phenotype of the Dnajb8 mutants. RESULTS: AlthoughDnajb8 is an evolutionarily conserved gene, it is not essential for spermatogenesis and male fertility. We provide this phenotypic information, which could prevent duplicative work by other groups. |
format | Online Article Text |
id | pubmed-7759119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77591192020-12-31 Dnajb8, a target gene of SOX30, is dispensable for male fertility in mice Wang, Fengsong Kong, Shuai Hu, Xuechun Li, Xin Xu, Bo Yue, Qiuling Fu, Kaiqiang Ye, Lan Bai, Shun PeerJ Developmental Biology BACKGROUND: The DNAJ family of molecular chaperones maintains protein homeostasis in mitotic and postmeiotic cells, especially germ cells. Recently, we found that the transcription factor SOX30 initiates transcription of Dnajb8 during late meiosis and spermiogenesis in mouse testes. METHODS: We used the CRISPR/Cas9 system to generate Dnajb8 mutant mice and analyze the phenotype of the Dnajb8 mutants. RESULTS: AlthoughDnajb8 is an evolutionarily conserved gene, it is not essential for spermatogenesis and male fertility. We provide this phenotypic information, which could prevent duplicative work by other groups. PeerJ Inc. 2020-12-21 /pmc/articles/PMC7759119/ /pubmed/33391882 http://dx.doi.org/10.7717/peerj.10582 Text en ©2020 Wang 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, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Developmental Biology Wang, Fengsong Kong, Shuai Hu, Xuechun Li, Xin Xu, Bo Yue, Qiuling Fu, Kaiqiang Ye, Lan Bai, Shun Dnajb8, a target gene of SOX30, is dispensable for male fertility in mice |
title | Dnajb8, a target gene of SOX30, is dispensable for male fertility in mice |
title_full | Dnajb8, a target gene of SOX30, is dispensable for male fertility in mice |
title_fullStr | Dnajb8, a target gene of SOX30, is dispensable for male fertility in mice |
title_full_unstemmed | Dnajb8, a target gene of SOX30, is dispensable for male fertility in mice |
title_short | Dnajb8, a target gene of SOX30, is dispensable for male fertility in mice |
title_sort | dnajb8, a target gene of sox30, is dispensable for male fertility in mice |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759119/ https://www.ncbi.nlm.nih.gov/pubmed/33391882 http://dx.doi.org/10.7717/peerj.10582 |
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