Deciphering balanced translocations in infertile males by next-generation sequencing to identify candidate genes for spermatogenesis disorders

Mol Hum Reprod. 2021 May 29;27(6):gaab034. doi: 10.1093/molehr/gaab034.

Abstract

Male infertility affects about 7% of the general male population. Balanced structural chromosomal rearrangements are observed in 0.4-1.4% of infertile males and are considered as a well-established cause of infertility. However, underlying pathophysiological mechanisms still need to be clarified. A strategy combining standard and high throughput cytogenetic and molecular technologies was applied in order to identify the candidate genes that might be implicated in the spermatogenesis defect in three male carriers of different balanced translocations. Fluorescence in situ hybridization (FISH) and whole-genome paired-end sequencing were used to characterize translocation breakpoints at the molecular level while exome sequencing was performed in order to exclude the presence of any molecular event independent from the chromosomal rearrangement in the patients. All translocation breakpoints were characterized in the three patients. We identified four variants: a position effect on LACTB2 gene in Patient 1, a heterozygous CTDP1 gene disruption in Patient 2, two single-nucleotide variations (SNVs) in DNAH5 gene and a heterozygous 17q12 deletion in Patient 3. The variants identified in this study need further validation to assess their roles in male infertility. This study shows that beside the mechanical effect of structural rearrangement on meiosis, breakpoints could result in additional alterations such as gene disruption or position effect. Moreover, additional SNVs or copy number variations may be fortuitously present and could explain the variable impact of chromosomal rearrangements on spermatogenesis. In conclusion, this study confirms the relevance of combining different cytogenetic and molecular techniques to investigate patients with spermatogenesis disorders and structural rearrangements on genomic scale.

Keywords: DNAH5; LACTB2; exome; genome sequencing; male infertility; translocation.

Publication types

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

MeSH terms

  • Adult
  • Asthenozoospermia / genetics
  • Axonemal Dyneins / genetics
  • Base Sequence
  • Chromosome Breakpoints
  • Exome Sequencing
  • Genetic Association Studies / methods*
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infertility, Male / genetics*
  • Male
  • Middle Aged
  • Phosphoprotein Phosphatases / genetics
  • Polymorphism, Single Nucleotide
  • Spermatogenesis / genetics*
  • Translocation, Genetic*
  • Whole Genome Sequencing
  • beta-Lactamases / genetics

Substances

  • Phosphoprotein Phosphatases
  • carboxy-terminal domain phosphatase
  • LACTB2 protein, human
  • beta-Lactamases
  • Axonemal Dyneins
  • DNAH5 protein, human