Literature DB >> 32638125

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

M J Xavier1, A Salas-Huetos2, M S Oud3, K I Aston4, J A Veltman5.   

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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Year:  2020        PMID: 32638125      PMCID: PMC7864819          DOI: 10.1007/s00439-020-02202-x

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  142 in total

1.  A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region.

Authors:  Isabel Martinez-Garay; Sibylle Jablonka; Marketa Sutajova; Peter Steuernagel; Andreas Gal; Kerstin Kutsche
Journal:  Genomics       Date:  2002-09       Impact factor: 5.736

2.  A case of human intersexuality having a possible XXY sex-determining mechanism.

Authors:  P A JACOBS; J A STRONG
Journal:  Nature       Date:  1959-01-31       Impact factor: 49.962

Review 3.  Genetics of male infertility.

Authors:  Csilla Krausz; Antoni Riera-Escamilla
Journal:  Nat Rev Urol       Date:  2018-06       Impact factor: 14.432

4.  Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm.

Authors:  D J Elliott; M R Millar; K Oghene; A Ross; F Kiesewetter; J Pryor; M McIntyre; T B Hargreave; P T Saunders; P H Vogt; A C Chandley; H Cooke
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-15       Impact factor: 11.205

5.  X-linked gene for testicular feminization in the mouse.

Authors:  M F Lyon; S G Hawkes
Journal:  Nature       Date:  1970-09-19       Impact factor: 49.962

6.  Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

Authors:  J R Riordan; J M Rommens; B Kerem; N Alon; R Rozmahel; Z Grzelczak; J Zielenski; S Lok; N Plavsic; J L Chou
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

7.  DPY19L2 deletion as a major cause of globozoospermia.

Authors:  Isabelle Koscinski; Elias Elinati; Camille Fossard; Claire Redin; Jean Muller; Juan Velez de la Calle; Françoise Schmitt; Mariem Ben Khelifa; Pierre F Ray; Pierre Ray; Zaid Kilani; Christopher L R Barratt; Stéphane Viville
Journal:  Am J Hum Genet       Date:  2011-03-11       Impact factor: 11.025

8.  The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results.

Authors:  P A Jacobs; A Frackiewicz; P Law; C J Hilditch; N E Morton
Journal:  Clin Genet       Date:  1975-09       Impact factor: 4.438

9.  Y chromosome gr/gr deletions are a risk factor for low semen quality.

Authors:  L Visser; G H Westerveld; C M Korver; S K M van Daalen; S E Hovingh; S Rozen; F van der Veen; S Repping
Journal:  Hum Reprod       Date:  2009-07-14       Impact factor: 6.918

10.  Evidence for a partial deletion in the androgen receptor gene in a phenotypic male with azoospermia.

Authors:  J W Akin; A Behzadian; S P Tho; P G McDonough
Journal:  Am J Obstet Gynecol       Date:  1991-12       Impact factor: 8.661

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  16 in total

1.  Genomic testing for copy number and single nucleotide variants in spermatogenic failure.

Authors:  J Hardy; N Pollock; T Gingrich; P Sweet; A Ramesh; J Kuong; A Basar; H Jiang; K Hwang; J Vukina; T Jaffe; M Olszewska; M Kurpisz; A N Yatsenko
Journal:  J Assist Reprod Genet       Date:  2022-07-18       Impact factor: 3.357

Review 2.  Spinal muscular atrophy: Broad disease spectrum and sex-specific phenotypes.

Authors:  Natalia N Singh; Shaine Hoffman; Prabhakara P Reddi; Ravindra N Singh
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2021-01-05       Impact factor: 5.187

3.  Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure.

Authors:  Jimmaline J Hardy; Margot J Wyrwoll; William Mcfadden; Agnieszka Malcher; Nadja Rotte; Nijole C Pollock; Sarah Munyoki; Maria V Veroli; Brendan J Houston; Miguel J Xavier; Laura Kasak; Margus Punab; Maris Laan; Sabine Kliesch; Peter Schlegel; Thomas Jaffe; Kathleen Hwang; Josip Vukina; Miguel A Brieño-Enríquez; Kyle Orwig; Judith Yanowitz; Michael Buszczak; Joris A Veltman; Manon Oud; Liina Nagirnaja; Marta Olszewska; Moira K O'Bryan; Donald F Conrad; Maciej Kurpisz; Frank Tüttelmann; Alexander N Yatsenko
Journal:  Hum Genet       Date:  2021-05-07       Impact factor: 5.881

4.  Role of testis‑specific serine kinase 1B in undiagnosed male infertility.

Authors:  Tanya Kadiyska; Ivan Tourtourikov; Kristiyan Dabchev; Dilyana Madzharova; Savina Tincheva; Demetrios A Spandidos; Vassilis Zoumpourlis
Journal:  Mol Med Rep       Date:  2022-04-29       Impact factor: 3.423

Review 5.  Insights from the Applications of Single-Cell Transcriptomic Analysis in Germ Cell Development and Reproductive Medicine.

Authors:  Hyeonwoo La; Hyunjin Yoo; Eun Joo Lee; Nguyen Xuan Thang; Hee Jin Choi; Jeongheon Oh; Ji Hyun Park; Kwonho Hong
Journal:  Int J Mol Sci       Date:  2021-01-15       Impact factor: 5.923

Review 6.  Obesity and Male Reproduction; Placing the Western Diet in Context.

Authors:  Taylor Pini; David Raubenheimer; Stephen J Simpson; Angela J Crean
Journal:  Front Endocrinol (Lausanne)       Date:  2021-03-11       Impact factor: 5.555

7.  Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.

Authors:  Albert Salas-Huetos; Frank Tüttelmann; Margot J Wyrwoll; Sabine Kliesch; Alexandra M Lopes; João Goncalves; Steven E Boyden; Marius Wöste; James M Hotaling; Liina Nagirnaja; Donald F Conrad; Douglas T Carrell; Kenneth I Aston
Journal:  Hum Genet       Date:  2020-11-19       Impact factor: 4.132

8.  Infertility due to defective sperm flagella caused by an intronic deletion in DNAH17 that perturbs splicing.

Authors:  Adéla Nosková; Maya Hiltpold; Fredi Janett; Thomas Echtermann; Zih-Hua Fang; Xaver Sidler; Christin Selige; Andreas Hofer; Stefan Neuenschwander; Hubert Pausch
Journal:  Genetics       Date:  2021-02-09       Impact factor: 4.562

9.  Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure.

Authors:  Thomas Eggermann
Journal:  Geburtshilfe Frauenheilkd       Date:  2021-07-13       Impact factor: 2.915

10.  Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.

Authors:  Xingxia Zhang; Ming Li; Xiaohua Jiang; Hui Ma; Suixing Fan; Yang Li; Changping Yu; Jianze Xu; Ranjha Khan; Hanwei Jiang; Qinghua Shi
Journal:  PLoS Genet       Date:  2021-08-13       Impact factor: 5.917

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