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FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation
The ubiquitin ligase SCF(FBXO38) controls centromeric chromatin by promoting the degradation of the ZXDB protein. To determine the importance of this pathway during development, Fbxo38-deficient mice were generated. The loss of FBXO38 resulted in growth retardation affecting several organs, includin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234700/ https://www.ncbi.nlm.nih.gov/pubmed/35769260 http://dx.doi.org/10.3389/fcell.2022.914053 |
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author | Dibus, Nikol Zobalova, Eliska Monleon, Mario A. M. Korinek, Vladimir Filipp, Dominik Petrusova, Jana Sedlacek, Radislav Kasparek, Petr Cermak, Lukas |
author_facet | Dibus, Nikol Zobalova, Eliska Monleon, Mario A. M. Korinek, Vladimir Filipp, Dominik Petrusova, Jana Sedlacek, Radislav Kasparek, Petr Cermak, Lukas |
author_sort | Dibus, Nikol |
collection | PubMed |
description | The ubiquitin ligase SCF(FBXO38) controls centromeric chromatin by promoting the degradation of the ZXDB protein. To determine the importance of this pathway during development, Fbxo38-deficient mice were generated. The loss of FBXO38 resulted in growth retardation affecting several organs, including the male reproductive system. A detailed analysis of the mutant testes revealed pathological changes in the seminiferous tubules, accompanied by a significant decrease in sperm production and reduced fertility. In adult testes, FBXO38 was specifically expressed in Sertoli cells, a somatic population essential for spermatogenesis initiation and progression. Sertoli cells lacking FBXO38 exhibited stabilized ZXDB protein and upregulated centromeric chromatin. Furthermore, the gene expression profile revealed that the absence of FBXO38 led to a defect in Sertoli cell maturation, specifically characterized by dysregulation in genes controlling retinoic acid metabolism and intercellular communication. Consequently, we documented significant changes in their ability to initiate spermatogonial differentiation. In conclusion, we show that FBXO38 acts as a Sertoli cell maturation factor, affecting the Sertoli cell transcription program, centromere integrity, and, subsequently, the ability to control spermatogenesis. |
format | Online Article Text |
id | pubmed-9234700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92347002022-06-28 FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation Dibus, Nikol Zobalova, Eliska Monleon, Mario A. M. Korinek, Vladimir Filipp, Dominik Petrusova, Jana Sedlacek, Radislav Kasparek, Petr Cermak, Lukas Front Cell Dev Biol Cell and Developmental Biology The ubiquitin ligase SCF(FBXO38) controls centromeric chromatin by promoting the degradation of the ZXDB protein. To determine the importance of this pathway during development, Fbxo38-deficient mice were generated. The loss of FBXO38 resulted in growth retardation affecting several organs, including the male reproductive system. A detailed analysis of the mutant testes revealed pathological changes in the seminiferous tubules, accompanied by a significant decrease in sperm production and reduced fertility. In adult testes, FBXO38 was specifically expressed in Sertoli cells, a somatic population essential for spermatogenesis initiation and progression. Sertoli cells lacking FBXO38 exhibited stabilized ZXDB protein and upregulated centromeric chromatin. Furthermore, the gene expression profile revealed that the absence of FBXO38 led to a defect in Sertoli cell maturation, specifically characterized by dysregulation in genes controlling retinoic acid metabolism and intercellular communication. Consequently, we documented significant changes in their ability to initiate spermatogonial differentiation. In conclusion, we show that FBXO38 acts as a Sertoli cell maturation factor, affecting the Sertoli cell transcription program, centromere integrity, and, subsequently, the ability to control spermatogenesis. Frontiers Media S.A. 2022-06-13 /pmc/articles/PMC9234700/ /pubmed/35769260 http://dx.doi.org/10.3389/fcell.2022.914053 Text en Copyright © 2022 Dibus, Zobalova, Monleon, Korinek, Filipp, Petrusova, Sedlacek, Kasparek and Cermak. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Dibus, Nikol Zobalova, Eliska Monleon, Mario A. M. Korinek, Vladimir Filipp, Dominik Petrusova, Jana Sedlacek, Radislav Kasparek, Petr Cermak, Lukas FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation |
title | FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation |
title_full | FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation |
title_fullStr | FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation |
title_full_unstemmed | FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation |
title_short | FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation |
title_sort | fbxo38 ubiquitin ligase controls sertoli cell maturation |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234700/ https://www.ncbi.nlm.nih.gov/pubmed/35769260 http://dx.doi.org/10.3389/fcell.2022.914053 |
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