Literature DB >> 33183966

Genetics of teratozoospermia: Back to the head.

Julie Beurois1, Caroline Cazin1, Zine-Eddine Kherraf2, Guillaume Martinez3, Tristan Celse3, Aminata Touré1, Christophe Arnoult1, Pierre F Ray2, Charles Coutton4.   

Abstract

Spermatozoa are polarized cells with a head and a flagellum joined by the connecting piece. Head integrity is critical for normal sperm function, and head defects consistently lead to male infertility. Abnormalities of the sperm head are among the most severe and characteristic sperm defects. Patients presenting with a monomorphic head sperm defects such as globozoospermia or marcrozoospermia were analyzed permitting to identify several key genes for spermatogenesis such as AURKC and DPY19L2. The study of patients with other specific sperm head defects such as acephalic spermatozoa have also enabled the identification of new infertility genes such as SUN5. Here, we review the genetic causes leading to morphological defects of sperm head. Advances in the genetics of male infertility are necessary to improve the management of infertility and will pave the road towards future strategies of treatments, especially for patients with the most severe phenotype as sperm head defects.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  acephalic spermatozoa; globozoospermia; intracytoplasmic sperm injection (ICSI); large headed spermatozoa; male infertility; teratozoospermia

Year:  2020        PMID: 33183966     DOI: 10.1016/j.beem.2020.101473

Source DB:  PubMed          Journal:  Best Pract Res Clin Endocrinol Metab        ISSN: 1521-690X            Impact factor:   4.690


  5 in total

Review 1.  Sperm bauplan and function and underlying processes of sperm formation and selection.

Authors:  Maria Eugenia Teves; Eduardo R S Roldan
Journal:  Physiol Rev       Date:  2021-04-21       Impact factor: 37.312

2.  Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa.

Authors:  Caroline Cazin; Yasmine Boumerdassi; Guillaume Martinez; Selima Fourati Ben Mustapha; Marjorie Whitfield; Charles Coutton; Nicolas Thierry-Mieg; Pierre Di Pizio; Nathalie Rives; Christophe Arnoult; Aminata Touré; Pierre F Ray; Raoudha Zouari; Christophe Sifer; Zine-Eddine Kherraf
Journal:  Int J Mol Sci       Date:  2021-02-22       Impact factor: 5.923

3.  Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B.

Authors:  Caroline Cazin; Yasmine Neirijnck; Corinne Loeuillet; Lydia Wehrli; Françoise Kühne; Isabelle Lordey; Selima Fourati Ben Mustapha; Amin Bouker; Raoudha Zouari; Nicolas Thierry-Mieg; Serge Nef; Christophe Arnoult; Pierre F Ray; Zine-Eddine Kherraf
Journal:  Cells       Date:  2021-12-30       Impact factor: 6.600

4.  Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice.

Authors:  Ranjha Khan; Qumar Zaman; Jing Chen; Manan Khan; Ao Ma; Jianteng Zhou; Beibei Zhang; Asim Ali; Muhammad Naeem; Muhammad Zubair; Daren Zhao; Wasim Shah; Mazhar Khan; Yuanwei Zhang; Bo Xu; Huan Zhang; Qinghua Shi
Journal:  Front Endocrinol (Lausanne)       Date:  2021-11-17       Impact factor: 5.555

5.  Oligogenic heterozygous inheritance of sperm abnormalities in mouse.

Authors:  Guillaume Martinez; Charles Coutton; Corinne Loeuillet; Caroline Cazin; Jana Muroňová; Magalie Boguenet; Emeline Lambert; Magali Dhellemmes; Geneviève Chevalier; Jean-Pascal Hograindleur; Charline Vilpreux; Yasmine Neirijnck; Zine-Eddine Kherraf; Jessica Escoffier; Serge Nef; Pierre F Ray; Christophe Arnoult
Journal:  Elife       Date:  2022-04-22       Impact factor: 8.713

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.