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A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review
BACKGROUND: Testis-expressed gene 11 (TEX11) is an X-linked gene and essential for meiotic recombination and chromosomal synapsis. TEX11 deficiency causes meiotic arrest and male infertility, and many TEX11 mutations have been found in azoospermic and infertile men. CASE PRESENTATION: This study rep...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902858/ https://www.ncbi.nlm.nih.gov/pubmed/29661171 http://dx.doi.org/10.1186/s12881-018-0570-4 |
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author | Sha, Yanwei Zheng, Liangkai Ji, Zhiyong Mei, Libin Ding, Lu Lin, Shaobin Wang, Xu Yang, Xiaoyu Li, Ping |
author_facet | Sha, Yanwei Zheng, Liangkai Ji, Zhiyong Mei, Libin Ding, Lu Lin, Shaobin Wang, Xu Yang, Xiaoyu Li, Ping |
author_sort | Sha, Yanwei |
collection | PubMed |
description | BACKGROUND: Testis-expressed gene 11 (TEX11) is an X-linked gene and essential for meiotic recombination and chromosomal synapsis. TEX11 deficiency causes meiotic arrest and male infertility, and many TEX11 mutations have been found in azoospermic and infertile men. CASE PRESENTATION: This study reported one novel TEX11 mutation (2653G → T, in exon 29, GenBank accession number, NM_031276) in two brothers with azoospermia. This mutation was firstly screened out by whole-exome sequencing (WES) and further verified by amplifying and sequencing the specific exon 29. Surprisingly, the same exonic missense mutation (W856C) was observed in two brothers but not in their mother. Histological analysis of testicular biopsy from both brothers revealed meiotic arrest and no post-meiotic round spermatids and mature spermatozoa were observed in the seminiferous tubules. TEX11 expression was observed strongly in spermatogonia and weakly in spermatocytes, but not in Sertoli cells and interstitial cells. CONCLUSIONS: We identified one novel TEX11 mutation in two brothers and summarized the literature regarding TEX11 mutations and male infertility. This study and previous literature indicate that TEX11 mutations are closely associated with male infertility, especially azoospermia, although auxiliary clinical analyses are needed to figure out the causes of male infertility. |
format | Online Article Text |
id | pubmed-5902858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59028582018-04-23 A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review Sha, Yanwei Zheng, Liangkai Ji, Zhiyong Mei, Libin Ding, Lu Lin, Shaobin Wang, Xu Yang, Xiaoyu Li, Ping BMC Med Genet Case Report BACKGROUND: Testis-expressed gene 11 (TEX11) is an X-linked gene and essential for meiotic recombination and chromosomal synapsis. TEX11 deficiency causes meiotic arrest and male infertility, and many TEX11 mutations have been found in azoospermic and infertile men. CASE PRESENTATION: This study reported one novel TEX11 mutation (2653G → T, in exon 29, GenBank accession number, NM_031276) in two brothers with azoospermia. This mutation was firstly screened out by whole-exome sequencing (WES) and further verified by amplifying and sequencing the specific exon 29. Surprisingly, the same exonic missense mutation (W856C) was observed in two brothers but not in their mother. Histological analysis of testicular biopsy from both brothers revealed meiotic arrest and no post-meiotic round spermatids and mature spermatozoa were observed in the seminiferous tubules. TEX11 expression was observed strongly in spermatogonia and weakly in spermatocytes, but not in Sertoli cells and interstitial cells. CONCLUSIONS: We identified one novel TEX11 mutation in two brothers and summarized the literature regarding TEX11 mutations and male infertility. This study and previous literature indicate that TEX11 mutations are closely associated with male infertility, especially azoospermia, although auxiliary clinical analyses are needed to figure out the causes of male infertility. BioMed Central 2018-04-16 /pmc/articles/PMC5902858/ /pubmed/29661171 http://dx.doi.org/10.1186/s12881-018-0570-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Sha, Yanwei Zheng, Liangkai Ji, Zhiyong Mei, Libin Ding, Lu Lin, Shaobin Wang, Xu Yang, Xiaoyu Li, Ping A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review |
title | A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review |
title_full | A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review |
title_fullStr | A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review |
title_full_unstemmed | A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review |
title_short | A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review |
title_sort | novel tex11 mutation induces azoospermia: a case report of infertile brothers and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902858/ https://www.ncbi.nlm.nih.gov/pubmed/29661171 http://dx.doi.org/10.1186/s12881-018-0570-4 |
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