Literature DB >> 24782004

Genetics of male fertility.

Yi-Nan Lin1, Martin M Matzuk.   

Abstract

Early in embryogenesis, cells that are destined to become germ cells take on a different destiny from other cells in the embryo. The germ cells are not programmed to perform "vital" functions but to perpetuate the species through the transfer of genetic materials to the next generation. To fulfill their destiny, male germ cells undergo meiosis and extensive morphogenesis that transforms the round-shaped cells into freely motile sperm propelled by a beating flagellum to seek out their missing half. Apparently, extra genes and additional regulatory mechanisms are required to achieve all these unique features, and an estimated 11 % of genes are involved in fertility in Drosophila (Hackstein et al., Trends Genet 16(12):565-572, 2000). If comparative numbers of male fertility genes are needed in mammals, extra risks of male fertility problems are associated with disruptive mutations in those genes. Among human male infertility cases, approximately 22 % were classified as "idiopathic," a term used to describe diseases of unknown causes, with idiopathic oligozoospermia being the most common semen abnormality (11.2 %) (Comhaire et al., Int J Androl (Suppl 7):1-53, 1987). "Idiopathic" is a widely used adjective that is used to reflect our lack of understanding of the genetics of male fertility. Fortunately, after more than two decades of phenotypic studies using knockout mice and identifying genes disrupted in spontaneous mutant mice, we have unveiled new and unexpected aspects of crucial gene functions for fertility. Other efforts to categorize genes involved in male fertility in mammals have suggested a total of 1,188 genes (Hermo et al., Microsc Res Tech 73(4):241-494, 2010). Although intracytoplasmic sperm injection (ICSI) can be used to bypass many fertilization obstacles to achieve fertilization with only a few extracted sperm, the widespread use of ICSI without proper knowledge for genetic testing and counseling could still potentially propagate pleiotropic gene mutations associated with male infertility and other genetic diseases (Alukal and Lamb, Urol Clin North Am 35(2):277-288, 2008). In this chapter, we give a brief account of major events during the development of male germ cells and focus on the functions of several crucial genes that have been studied in mutant mouse models and are potential causes of human male infertility.

Entities:  

Mesh:

Year:  2014        PMID: 24782004     DOI: 10.1007/978-1-4939-0659-8_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  8 in total

Review 1.  Precision Medicine and Men's Health.

Authors:  Douglas A Mata; Farhan M Katchi; Ranjith Ramasamy
Journal:  Am J Mens Health       Date:  2015-07-17

2.  Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L.

Authors:  Ayobami Ward; Jessica Hopkins; Matthew Mckay; Steve Murray; Philip W Jordan
Journal:  G3 (Bethesda)       Date:  2016-06-01       Impact factor: 3.154

Review 3.  Contribution of Single-Cell Transcriptomics to the Characterization of Human Spermatogonial Stem Cells: Toward an Application in Male Fertility Regenerative Medicine?

Authors:  Anne-Sophie Gille; Clémentine Lapoujade; Jean-Philippe Wolf; Pierre Fouchet; Virginie Barraud-Lange
Journal:  Int J Mol Sci       Date:  2019-11-16       Impact factor: 5.923

4.  The Mechanism and Experimental Validation of Forsythoside A in the Treatment of Male Infertility Were Analyzed Based on Network Pharmacology and Molecular Docking.

Authors:  Zhen Ma; Xueling Liu; Haiwang Lu; Haoming Li; Ruizhi Gao; Rong Wen; Zhiping Tang; Haihui Yin; Yun He; Hong Yang
Journal:  Evid Based Complement Alternat Med       Date:  2022-10-06       Impact factor: 2.650

5.  Discovering in vitro spermatogenesis stimulating factors.

Authors:  J Chaudhary; F K Hamra
Journal:  Cell Death Dis       Date:  2015-10-22       Impact factor: 8.469

6.  A systematic review on the genetics of male infertility in the era of next-generation sequencing.

Authors:  Amal Robay; Saleha Abbasi; Ammira Akil; Haitham El-Bardisi; Mohamed Arafa; Ronald G Crystal; Khalid A Fakhro
Journal:  Arab J Urol       Date:  2018-02-14

7.  A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR.

Authors:  Satu Wedenoja; Ahlam Khamaysi; Liana Shimshilashvili; Shireen Anbtawe-Jomaa; Outi Elomaa; Jorma Toppari; Pia Höglund; Kristiina Aittomäki; Christer Holmberg; Outi Hovatta; Juha S Tapanainen; Ehud Ohana; Juha Kere
Journal:  Sci Rep       Date:  2017-10-27       Impact factor: 4.379

8.  Efficient GFP-labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry.

Authors:  Leah L Zagore; Cydni C Akesson; Donny D Licatalosi
Journal:  Genesis       Date:  2019-02-06       Impact factor: 2.487

  8 in total

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