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Homeodomain protein HOMEZ is dispensable for male fertility in mice

BACKGROUND: Homeodomain (HD) proteins contain an evolutionarily conserved helix-turn-helix (HTH) DNA-binding motif and act as transcription factors to control gene expression. A previous study showed that the HD gene Homez is highly enriched in adult testes. However, the role of HOMEZ in spermatogen...

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Autores principales: Yue, Qiuling, Yu, Lina, Liu, Wenwen, Zhou, Jidong, Hu, Xuechun, Liu, Yixun, Zhou, Xue, Wu, Limin, Xu, Bo, Tong, Xianhong, Jiang, Xiaohua, Yan, Guijun, Bai, Shun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262745/
https://www.ncbi.nlm.nih.gov/pubmed/35812194
http://dx.doi.org/10.21037/tau-21-1169
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author Yue, Qiuling
Yu, Lina
Liu, Wenwen
Zhou, Jidong
Hu, Xuechun
Liu, Yixun
Zhou, Xue
Wu, Limin
Xu, Bo
Tong, Xianhong
Jiang, Xiaohua
Yan, Guijun
Bai, Shun
author_facet Yue, Qiuling
Yu, Lina
Liu, Wenwen
Zhou, Jidong
Hu, Xuechun
Liu, Yixun
Zhou, Xue
Wu, Limin
Xu, Bo
Tong, Xianhong
Jiang, Xiaohua
Yan, Guijun
Bai, Shun
author_sort Yue, Qiuling
collection PubMed
description BACKGROUND: Homeodomain (HD) proteins contain an evolutionarily conserved helix-turn-helix (HTH) DNA-binding motif and act as transcription factors to control gene expression. A previous study showed that the HD gene Homez is highly enriched in adult testes. However, the role of HOMEZ in spermatogenesis and male fertility remains unknown. METHODS: Using CRISPR/Cas9 technology, Homez mutant mice were generated and performed histological, immunofluorescence, quantitative reverse transcription-polymerase chain reaction (qRT-PCR), Western blot and mating assays to analyze the phenotype of Homez mutants. RESULTS: Molecular phylogenetic analyses indicated that the HOMEZ is evolutionarily conserved among mammalian species. qRT-PCR and Western blot analyses showed that Homez is highly expressed in the testis, with a relatively increased expression trend during spermatogenesis. Homez mutant males were viable and showed no differences in body and testis weight compared to their wild-type. In addition, mating between Homez mutant males and wild-type females produced normal litter sizes. Moreover, histopathology detected complete spermatogenesis in the seminiferous tubules and mature spermatozoa in the epididymides from Homez knockout males. Furthermore, significantly increased transcription of three Zhx genes were found in Homez mutatnt testes compared with wild-type testes. CONCLUSIONS: Homez knockout mice are fertile and are not essential for germ cell development. These findings could prevent unnecessary duplicative work by other groups.
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spelling pubmed-92627452022-07-09 Homeodomain protein HOMEZ is dispensable for male fertility in mice Yue, Qiuling Yu, Lina Liu, Wenwen Zhou, Jidong Hu, Xuechun Liu, Yixun Zhou, Xue Wu, Limin Xu, Bo Tong, Xianhong Jiang, Xiaohua Yan, Guijun Bai, Shun Transl Androl Urol Original Article BACKGROUND: Homeodomain (HD) proteins contain an evolutionarily conserved helix-turn-helix (HTH) DNA-binding motif and act as transcription factors to control gene expression. A previous study showed that the HD gene Homez is highly enriched in adult testes. However, the role of HOMEZ in spermatogenesis and male fertility remains unknown. METHODS: Using CRISPR/Cas9 technology, Homez mutant mice were generated and performed histological, immunofluorescence, quantitative reverse transcription-polymerase chain reaction (qRT-PCR), Western blot and mating assays to analyze the phenotype of Homez mutants. RESULTS: Molecular phylogenetic analyses indicated that the HOMEZ is evolutionarily conserved among mammalian species. qRT-PCR and Western blot analyses showed that Homez is highly expressed in the testis, with a relatively increased expression trend during spermatogenesis. Homez mutant males were viable and showed no differences in body and testis weight compared to their wild-type. In addition, mating between Homez mutant males and wild-type females produced normal litter sizes. Moreover, histopathology detected complete spermatogenesis in the seminiferous tubules and mature spermatozoa in the epididymides from Homez knockout males. Furthermore, significantly increased transcription of three Zhx genes were found in Homez mutatnt testes compared with wild-type testes. CONCLUSIONS: Homez knockout mice are fertile and are not essential for germ cell development. These findings could prevent unnecessary duplicative work by other groups. AME Publishing Company 2022-06 /pmc/articles/PMC9262745/ /pubmed/35812194 http://dx.doi.org/10.21037/tau-21-1169 Text en 2022 Translational Andrology and Urology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Yue, Qiuling
Yu, Lina
Liu, Wenwen
Zhou, Jidong
Hu, Xuechun
Liu, Yixun
Zhou, Xue
Wu, Limin
Xu, Bo
Tong, Xianhong
Jiang, Xiaohua
Yan, Guijun
Bai, Shun
Homeodomain protein HOMEZ is dispensable for male fertility in mice
title Homeodomain protein HOMEZ is dispensable for male fertility in mice
title_full Homeodomain protein HOMEZ is dispensable for male fertility in mice
title_fullStr Homeodomain protein HOMEZ is dispensable for male fertility in mice
title_full_unstemmed Homeodomain protein HOMEZ is dispensable for male fertility in mice
title_short Homeodomain protein HOMEZ is dispensable for male fertility in mice
title_sort homeodomain protein homez is dispensable for male fertility in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262745/
https://www.ncbi.nlm.nih.gov/pubmed/35812194
http://dx.doi.org/10.21037/tau-21-1169
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