Genetics of teratozoospermia: Back to the head

Best Pract Res Clin Endocrinol Metab. 2020 Dec;34(6):101473. doi: 10.1016/j.beem.2020.101473. Epub 2020 Nov 2.

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.

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

Publication types

  • Review

MeSH terms

  • Aurora Kinase C / genetics
  • Humans
  • Infertility, Male / genetics
  • Infertility, Male / pathology
  • Male
  • Membrane Proteins / genetics
  • Sperm Head / metabolism
  • Sperm Head / pathology*
  • Spermatogenesis / genetics
  • Spermatozoa / abnormalities*
  • Spermatozoa / metabolism
  • Spermatozoa / pathology
  • Teratozoospermia / genetics*
  • Teratozoospermia / pathology

Substances

  • DPY19L2 protein, human
  • Membrane Proteins
  • SUN5 protein, human
  • AURKC protein, human
  • Aurora Kinase C