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Disease Gene Discovery in Male Infertility: Past, Present and Future

Overview
Journal Hum Genet
Specialty Genetics
Date 2020 Jul 9
PMID 32638125
Citations 37
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Abstract

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.

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References
1.
Koscinski I, Elinati E, Fossard C, Redin C, Muller J, Velez de la Calle J . DPY19L2 deletion as a major cause of globozoospermia. Am J Hum Genet. 2011; 88(3):344-50. PMC: 3059416. DOI: 10.1016/j.ajhg.2011.01.018. View

2.
Martinez-Garay I, Jablonka S, Sutajova M, Steuernagel P, Gal A, Kutsche K . A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region. Genomics. 2002; 80(3):259-67. DOI: 10.1006/geno.2002.6834. View

3.
Lyon M, Hawkes S . X-linked gene for testicular feminization in the mouse. Nature. 1970; 227(5264):1217-9. DOI: 10.1038/2271217a0. View

4.
Jacobs P, Strong J . A case of human intersexuality having a possible XXY sex-determining mechanism. Nature. 1959; 183(4657):302-3. DOI: 10.1038/183302a0. View

5.
Jacobs P, Frackiewicz A, Law P, Hilditch C, Morton N . The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results. Clin Genet. 1975; 8(3):169-78. DOI: 10.1111/j.1399-0004.1975.tb01490.x. View