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Characterization of the promoter region of the murine Catsper2 gene
CATSPER2 (Cation channel sperm‐associated protein 2) protein, which is part of the calcium CATSPER channel located in the membrane of the flagellar principal piece of the sperm cell, is only expressed in the testis during spermatogenesis. Deletions or mutations in the Catsper2 gene are associated wi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714369/ https://www.ncbi.nlm.nih.gov/pubmed/36345591 http://dx.doi.org/10.1002/2211-5463.13518 |
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author | Contreras‐Marciales, Andrea del Pilar López‐Guzmán, Sergio Federico Benítez‐Hess, María Luisa Oviedo, Norma Hernández‐Sánchez, Javier |
author_facet | Contreras‐Marciales, Andrea del Pilar López‐Guzmán, Sergio Federico Benítez‐Hess, María Luisa Oviedo, Norma Hernández‐Sánchez, Javier |
author_sort | Contreras‐Marciales, Andrea del Pilar |
collection | PubMed |
description | CATSPER2 (Cation channel sperm‐associated protein 2) protein, which is part of the calcium CATSPER channel located in the membrane of the flagellar principal piece of the sperm cell, is only expressed in the testis during spermatogenesis. Deletions or mutations in the Catsper2 gene are associated with the deafness‐infertility syndrome (DIS) and non‐syndromic male infertility. However, the mechanisms by which Catsper2 is regulated are unknown. Here, we report the characterization of the promoter region of murine Catsper2 and the role of CTCF and CREMτ in its transcription. We report that the promoter region has transcriptional activity in both directions, as determined by observing luciferase activity in mouse Sertoli and GC‐1 spg transfected cells. WGBS data analysis indicated that a CpG island identified in silico is non‐methylated; Chromatin immunoprecipitation (ChIP)‐seq data analysis revealed that histone marks H3K4me3 and H3K36me3 are present in the promoter and body of the Catsper2 gene respectively, indicating that Catsper2 is subject to epigenetic regulation. In addition, the murine Catsper2 core promoter was delimited to a region between −54/+189 relative to the transcription start site (TSS), where three CTCF and one CRE binding site were predicted. The functionality of these sites was determined by mutation of the CTCF sites and deletion of the CRE site. Finally, ChIP assays confirmed that CREMτ and CTCF bind to the Catsper2 minimal promoter region. This study represents the first functional analysis of the murine Catsper2 promoter region and the mechanisms that regulate its expression. |
format | Online Article Text |
id | pubmed-9714369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97143692022-12-02 Characterization of the promoter region of the murine Catsper2 gene Contreras‐Marciales, Andrea del Pilar López‐Guzmán, Sergio Federico Benítez‐Hess, María Luisa Oviedo, Norma Hernández‐Sánchez, Javier FEBS Open Bio Research Articles CATSPER2 (Cation channel sperm‐associated protein 2) protein, which is part of the calcium CATSPER channel located in the membrane of the flagellar principal piece of the sperm cell, is only expressed in the testis during spermatogenesis. Deletions or mutations in the Catsper2 gene are associated with the deafness‐infertility syndrome (DIS) and non‐syndromic male infertility. However, the mechanisms by which Catsper2 is regulated are unknown. Here, we report the characterization of the promoter region of murine Catsper2 and the role of CTCF and CREMτ in its transcription. We report that the promoter region has transcriptional activity in both directions, as determined by observing luciferase activity in mouse Sertoli and GC‐1 spg transfected cells. WGBS data analysis indicated that a CpG island identified in silico is non‐methylated; Chromatin immunoprecipitation (ChIP)‐seq data analysis revealed that histone marks H3K4me3 and H3K36me3 are present in the promoter and body of the Catsper2 gene respectively, indicating that Catsper2 is subject to epigenetic regulation. In addition, the murine Catsper2 core promoter was delimited to a region between −54/+189 relative to the transcription start site (TSS), where three CTCF and one CRE binding site were predicted. The functionality of these sites was determined by mutation of the CTCF sites and deletion of the CRE site. Finally, ChIP assays confirmed that CREMτ and CTCF bind to the Catsper2 minimal promoter region. This study represents the first functional analysis of the murine Catsper2 promoter region and the mechanisms that regulate its expression. John Wiley and Sons Inc. 2022-11-17 /pmc/articles/PMC9714369/ /pubmed/36345591 http://dx.doi.org/10.1002/2211-5463.13518 Text en © 2022 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Contreras‐Marciales, Andrea del Pilar López‐Guzmán, Sergio Federico Benítez‐Hess, María Luisa Oviedo, Norma Hernández‐Sánchez, Javier Characterization of the promoter region of the murine Catsper2 gene |
title | Characterization of the promoter region of the murine Catsper2 gene |
title_full | Characterization of the promoter region of the murine Catsper2 gene |
title_fullStr | Characterization of the promoter region of the murine Catsper2 gene |
title_full_unstemmed | Characterization of the promoter region of the murine Catsper2 gene |
title_short | Characterization of the promoter region of the murine Catsper2 gene |
title_sort | characterization of the promoter region of the murine catsper2 gene |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714369/ https://www.ncbi.nlm.nih.gov/pubmed/36345591 http://dx.doi.org/10.1002/2211-5463.13518 |
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