Gene polymorphisms/mutations relevant to abnormal spermatogenesis

Reprod Biomed Online. 2008 Apr;16(4):504-13. doi: 10.1016/s1472-6483(10)60457-9.

Abstract

Despite the identification of an increasing number of candidate genes involved in spermatogenesis, the armamentarium of diagnostic genetic tests in male infertility remains extremely limited. A number of new causative mutations have been reported for hypogonadotrophic hypogonadism but still the genetic diagnosis in this pathological condition is made only in about 20% of cases. The sole molecular genetic test that is routinely proposed in severe spermatogenic disturbances is screening for Yq microdeletion. The search for causative mutations in the Y chromosome, and in autosomal and X-linked genes, has mostly been unsuccessful. The paucity of gene mutations raises questions about the appropriateness of the currently used screening approaches. Among the proposed genetic risk factors, gr/gr deletion of the Y chromosome seems to be the most promising polymorphism. Other polymorphisms are awaiting further confirmation, whereas for some (POLG, DAZL, USP26, FSHR) a lack of association with abnormal spermatogenesis has now been ascertained. It is likely that some polymorphisms lead to testicular dysfunction only when in association with a specific genetic background or with environmental factors. Future large-scale studies with stringent study design may provide a more efficient way to identify clinically relevant genetic factors of male infertility.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Genes / physiology
  • Genetic Loci
  • Genetic Predisposition to Disease
  • Gonadotropins / deficiency
  • Humans
  • Infertility, Male / genetics*
  • Male
  • Mutation* / physiology
  • Polymorphism, Single Nucleotide*
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Seminal Plasma Proteins / genetics
  • Spermatogenesis / genetics*
  • Y Chromosome / genetics

Substances

  • Gonadotropins
  • Receptors, Cytoplasmic and Nuclear
  • Seminal Plasma Proteins