Web of Science: 50 citations, Scopus: 55 citations, Google Scholar: citations,
The X chromosome and male infertility
Vockel, Matthias (University of Münster. Institute of Human Genetics)
Riera-Escamilla, Antoni (Institut d'Investigació Biomèdica Sant Pau)
Tüttelmann, Frank (University of Münster. Institute of Human Genetics)
Krausz, Csilla (Institut d'Investigació Biomèdica Sant Pau)
Universitat Autònoma de Barcelona

Date: 2019
Abstract: The X chromosome is a key player in germ cell development, as has been highlighted for males in previous studies revealing that the mammalian X chromosome is enriched in genes expressed in early spermatogenesis. In this review, we focus on the X chromosome's unique biology as associated with human male infertility. Male infertility is most commonly caused by spermatogenic defects to which X chromosome dosage is closely linked; for example, any supernumerary X chromosome as in Klinefelter syndrome will lead to male infertility. Furthermore, because males normally only have a single X chromosome and because X-linked genetic anomalies are generally only present in a single copy in males, any loss-of-function mutations in single-copy X-chromosomal genes cannot be compensated by a normal allele. These features make X-linked genes particularly attractive for studying male spermatogenic failure. However, to date, only very few genetic causes have been identified as being definitively responsible for male infertility in humans. Although genetic studies of germ cell-enriched X-chromosomal genes in mice suggest a role of certain human orthologs in infertile men, these genes in mice and humans have striking evolutionary differences. Furthermore, the complexity and highly repetitive structure of the X chromosome hinder the mutational analysis of X-linked genes in humans. Therefore, we conclude that additional methodological approaches are urgently warranted to advance our understanding of the genetics of X-linked male infertility.
Grants: Instituto de Salud Carlos III FIS-FEDER-PI14-01250
Instituto de Salud Carlos III PI17-01822
European Commission 289880
Rights: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Language: Anglès
Document: Article de revisió ; Article ; Versió publicada
Published in: Human Genetics, Vol. 140 (december 2019) , p. 203-215, ISSN 1432-1203

DOI: 10.1007/s00439-019-02101-w
PMID: 31875237


13 p, 710.6 KB

The record appears in these collections:
Research literature > UAB research groups literature > Research Centres and Groups (research output) > Health sciences and biosciences > Institut de Recerca Sant Pau
Articles > Published articles

 Record created 2021-02-22, last modified 2023-11-30



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