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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...

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Autores principales: Dibus, Nikol, Zobalova, Eliska, Monleon, Mario A. M., Korinek, Vladimir, Filipp, Dominik, Petrusova, Jana, Sedlacek, Radislav, Kasparek, Petr, Cermak, Lukas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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.
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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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