Cargando…
ZDHHC19 Is Dispensable for Spermatogenesis, but Is Essential for Sperm Functions in Mice
Spermatogenesis is a complicated process involving mitotically proliferating spermatogonial cells, meiotically dividing spermatocytes, and spermatid going through maturation into spermatozoa. The post-translational modifications of proteins play important roles in this biological process. S-palmitoy...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396176/ https://www.ncbi.nlm.nih.gov/pubmed/34445597 http://dx.doi.org/10.3390/ijms22168894 |
_version_ | 1783744312259903488 |
---|---|
author | Wang, Shuai Qiao, Hongjie Wang, Pengxiang Wang, Yuan Qin, Danian |
author_facet | Wang, Shuai Qiao, Hongjie Wang, Pengxiang Wang, Yuan Qin, Danian |
author_sort | Wang, Shuai |
collection | PubMed |
description | Spermatogenesis is a complicated process involving mitotically proliferating spermatogonial cells, meiotically dividing spermatocytes, and spermatid going through maturation into spermatozoa. The post-translational modifications of proteins play important roles in this biological process. S-palmitoylation is one type of protein modifications catalyzed by zinc finger Asp-His-His-Cys (ZDHHC)-family palmitoyl S-acyltransferases. There are 23 mammalian ZDHHCs that have been identified in mouse. Among them, Zdhhc19 is highly expressed in adult testis. However, the in vivo function of Zdhhc19 in mouse spermatogenesis and fertility remains unknown. In this study, we knocked out the Zdhhc19 gene by generating a 2609 bp deletion from exon 3 to exon 6 in mice. No differences were found in testis morphology and testis/body weight ratios upon Zdhhc19 deletion. Spermatogenesis was not disrupted in Zdhhc19 knockout mice, in which properly developed TRA98+ germ cells, SYCP3+ spermatocytes, and TNP1+ spermatids/spermatozoa were detected in seminiferous tubules. Nevertheless, Zdhhc19 knockout mice were male infertile. Zdhhc19 deficient spermatozoa exhibited multiple defects including abnormal morphology of sperm tails and heads, decreased motility, and disturbed acrosome reaction. All of these led to the inability of Zdhhc19 mutant sperm to fertilize oocytes in IVF assays. Taken together, our results support the fact that Zdhhc19 is a testis enriched gene dispensable for spermatogenesis, but is essential for sperm functions in mice. |
format | Online Article Text |
id | pubmed-8396176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83961762021-08-28 ZDHHC19 Is Dispensable for Spermatogenesis, but Is Essential for Sperm Functions in Mice Wang, Shuai Qiao, Hongjie Wang, Pengxiang Wang, Yuan Qin, Danian Int J Mol Sci Article Spermatogenesis is a complicated process involving mitotically proliferating spermatogonial cells, meiotically dividing spermatocytes, and spermatid going through maturation into spermatozoa. The post-translational modifications of proteins play important roles in this biological process. S-palmitoylation is one type of protein modifications catalyzed by zinc finger Asp-His-His-Cys (ZDHHC)-family palmitoyl S-acyltransferases. There are 23 mammalian ZDHHCs that have been identified in mouse. Among them, Zdhhc19 is highly expressed in adult testis. However, the in vivo function of Zdhhc19 in mouse spermatogenesis and fertility remains unknown. In this study, we knocked out the Zdhhc19 gene by generating a 2609 bp deletion from exon 3 to exon 6 in mice. No differences were found in testis morphology and testis/body weight ratios upon Zdhhc19 deletion. Spermatogenesis was not disrupted in Zdhhc19 knockout mice, in which properly developed TRA98+ germ cells, SYCP3+ spermatocytes, and TNP1+ spermatids/spermatozoa were detected in seminiferous tubules. Nevertheless, Zdhhc19 knockout mice were male infertile. Zdhhc19 deficient spermatozoa exhibited multiple defects including abnormal morphology of sperm tails and heads, decreased motility, and disturbed acrosome reaction. All of these led to the inability of Zdhhc19 mutant sperm to fertilize oocytes in IVF assays. Taken together, our results support the fact that Zdhhc19 is a testis enriched gene dispensable for spermatogenesis, but is essential for sperm functions in mice. MDPI 2021-08-18 /pmc/articles/PMC8396176/ /pubmed/34445597 http://dx.doi.org/10.3390/ijms22168894 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Shuai Qiao, Hongjie Wang, Pengxiang Wang, Yuan Qin, Danian ZDHHC19 Is Dispensable for Spermatogenesis, but Is Essential for Sperm Functions in Mice |
title | ZDHHC19 Is Dispensable for Spermatogenesis, but Is Essential for Sperm Functions in Mice |
title_full | ZDHHC19 Is Dispensable for Spermatogenesis, but Is Essential for Sperm Functions in Mice |
title_fullStr | ZDHHC19 Is Dispensable for Spermatogenesis, but Is Essential for Sperm Functions in Mice |
title_full_unstemmed | ZDHHC19 Is Dispensable for Spermatogenesis, but Is Essential for Sperm Functions in Mice |
title_short | ZDHHC19 Is Dispensable for Spermatogenesis, but Is Essential for Sperm Functions in Mice |
title_sort | zdhhc19 is dispensable for spermatogenesis, but is essential for sperm functions in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396176/ https://www.ncbi.nlm.nih.gov/pubmed/34445597 http://dx.doi.org/10.3390/ijms22168894 |
work_keys_str_mv | AT wangshuai zdhhc19isdispensableforspermatogenesisbutisessentialforspermfunctionsinmice AT qiaohongjie zdhhc19isdispensableforspermatogenesisbutisessentialforspermfunctionsinmice AT wangpengxiang zdhhc19isdispensableforspermatogenesisbutisessentialforspermfunctionsinmice AT wangyuan zdhhc19isdispensableforspermatogenesisbutisessentialforspermfunctionsinmice AT qindanian zdhhc19isdispensableforspermatogenesisbutisessentialforspermfunctionsinmice |