Disease gene discovery in male infertility: past, present and future

被引:44
|
作者
Xavier, M. J. [1 ]
Salas-Huetos, A. [2 ]
Oud, M. S. [3 ]
Aston, K. I. [2 ]
Veltman, J. A. [1 ]
机构
[1] Newcastle Univ, Biosci Inst, Fac Med Sci, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Utah, Androl & IVF Lab, Dept Surg Urol, Salt Lake City, UT 84112 USA
[3] Radboud Univ Nijmegen, Dept Human Genet, Med Ctr, Nijmegen, Netherlands
基金
美国国家卫生研究院; 英国惠康基金;
关键词
ANDROGEN RECEPTOR GENE; COMPARATIVE GENOMIC HYBRIDIZATION; CYSTIC-FIBROSIS GENE; HUMAN Y-CHROMOSOME; CONGENITAL BILATERAL ABSENCE; AZF-CANDIDATE GENES; ENU MUTAGENESIS; MALE-FERTILITY; AZOOSPERMIC MEN; SPERMATOGENIC FAILURE;
D O I
10.1007/s00439-020-02202-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Identifying the genes causing male infertility is important to increase our biological understanding as well as the diagnostic yield and clinical relevance of genetic testing in this disorder. While significant progress has been made in some areas, mainly in our knowledge of the genes underlying rare qualitative sperm defects, the same cannot be said for the genetics of quantitative sperm defects. Technological advances and approaches in genomics are critical for the process of disease gene identification. In this review we highlight the impact of various technological developments on male infertility gene discovery as well as functional validation, going from the past to the present and the future. In particular, we draw attention to the use of unbiased genomics approaches, the development of increasingly relevant functional assays and the importance of large-scale international collaboration to advance disease gene identification in male infertility.
引用
收藏
页码:7 / 19
页数:13
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