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Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice

Infertility affects 10–15% of couples worldwide, and male factors account for 50%. Spermatogenesis is precisely regulated by genetic factors, and the mutations of genes result in abnormal spermatogenesis and eventual male infertility. The aim of this study was to explore the role and transcriptional...

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Autores principales: Wang, Hong, Yuan, Qingqing, Niu, Minghui, Zhang, Wenhui, Wen, Liping, Fu, Hongyong, Zhou, Fan, He, Zuping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833356/
https://www.ncbi.nlm.nih.gov/pubmed/29362488
http://dx.doi.org/10.1038/s41419-017-0046-z
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author Wang, Hong
Yuan, Qingqing
Niu, Minghui
Zhang, Wenhui
Wen, Liping
Fu, Hongyong
Zhou, Fan
He, Zuping
author_facet Wang, Hong
Yuan, Qingqing
Niu, Minghui
Zhang, Wenhui
Wen, Liping
Fu, Hongyong
Zhou, Fan
He, Zuping
author_sort Wang, Hong
collection PubMed
description Infertility affects 10–15% of couples worldwide, and male factors account for 50%. Spermatogenesis is precisely regulated by genetic factors, and the mutations of genes result in abnormal spermatogenesis and eventual male infertility. The aim of this study was to explore the role and transcriptional regulation of P63 in the apoptosis and mouse spermatogenesis. P63 protein was decreased in male germ cells of P63((+/−)) mice compared with wild-type mice. There was no obvious difference in testis weight, sperm motility, and fecundity between P63((+/−)) and wild-type mice. However, abnormal germ cells were frequently observed in P63((+/−)) mice at 2 months old. Notably, apoptotic male germ cells and the percentage of abnormal sperm were significantly enhanced in P63((+/−)) mice compared to wild-type mice. Spermatogonia, pachytene spermatocytes and round spermatids were isolated from P63((+/−)) and wild-type mice using STA-PUT velocity sedimentation, and they were identified phenotypically with high purities. RNA sequencing demonstrated distinct transcription profiles in spermatogonia, pachytene spermatocytes, and round spermatids between P63((+/−)) mice and wild-type mice. In total, there were 645 differentially expressed genes (DEGs) in spermatogonia, 106 DEGs in pachytene spermatocytes, and 1152 in round spermatids between P63((+/−)) mice and wild-type mice. Real time PCR verified a number of DEGs identified by RNA sequencing. Gene ontology annotation and pathway analyzes further indicated that certain key genes, e.g., Ccnd2, Tgfa, Hes5, Insl3, Kit, Lef1, and Jun were involved in apoptosis, while Dazl, Kit, Pld6, Cdkn2d, Stra8, and Ubr2 were associated with regulating spermatogenesis. Collectively, these results implicate that P63 mediates the apoptosis of male germ cells and regulates three stages of spermatogenesis transcriptionally. This study could provide novel targets for the diagnosis and treatment of male infertility.
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spelling pubmed-58333562018-03-05 Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice Wang, Hong Yuan, Qingqing Niu, Minghui Zhang, Wenhui Wen, Liping Fu, Hongyong Zhou, Fan He, Zuping Cell Death Dis Article Infertility affects 10–15% of couples worldwide, and male factors account for 50%. Spermatogenesis is precisely regulated by genetic factors, and the mutations of genes result in abnormal spermatogenesis and eventual male infertility. The aim of this study was to explore the role and transcriptional regulation of P63 in the apoptosis and mouse spermatogenesis. P63 protein was decreased in male germ cells of P63((+/−)) mice compared with wild-type mice. There was no obvious difference in testis weight, sperm motility, and fecundity between P63((+/−)) and wild-type mice. However, abnormal germ cells were frequently observed in P63((+/−)) mice at 2 months old. Notably, apoptotic male germ cells and the percentage of abnormal sperm were significantly enhanced in P63((+/−)) mice compared to wild-type mice. Spermatogonia, pachytene spermatocytes and round spermatids were isolated from P63((+/−)) and wild-type mice using STA-PUT velocity sedimentation, and they were identified phenotypically with high purities. RNA sequencing demonstrated distinct transcription profiles in spermatogonia, pachytene spermatocytes, and round spermatids between P63((+/−)) mice and wild-type mice. In total, there were 645 differentially expressed genes (DEGs) in spermatogonia, 106 DEGs in pachytene spermatocytes, and 1152 in round spermatids between P63((+/−)) mice and wild-type mice. Real time PCR verified a number of DEGs identified by RNA sequencing. Gene ontology annotation and pathway analyzes further indicated that certain key genes, e.g., Ccnd2, Tgfa, Hes5, Insl3, Kit, Lef1, and Jun were involved in apoptosis, while Dazl, Kit, Pld6, Cdkn2d, Stra8, and Ubr2 were associated with regulating spermatogenesis. Collectively, these results implicate that P63 mediates the apoptosis of male germ cells and regulates three stages of spermatogenesis transcriptionally. This study could provide novel targets for the diagnosis and treatment of male infertility. Nature Publishing Group UK 2018-01-23 /pmc/articles/PMC5833356/ /pubmed/29362488 http://dx.doi.org/10.1038/s41419-017-0046-z Text en © The Author(s) 2018 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
Wang, Hong
Yuan, Qingqing
Niu, Minghui
Zhang, Wenhui
Wen, Liping
Fu, Hongyong
Zhou, Fan
He, Zuping
Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice
title Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice
title_full Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice
title_fullStr Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice
title_full_unstemmed Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice
title_short Transcriptional regulation of P63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice
title_sort transcriptional regulation of p63 on the apoptosis of male germ cells and three stages of spermatogenesis in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833356/
https://www.ncbi.nlm.nih.gov/pubmed/29362488
http://dx.doi.org/10.1038/s41419-017-0046-z
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