Single-nucleotide polymorphisms and mutation analyses of the TNP1 and TNP2 genes of fertile and infertile human male populations

J Androl. 2005 Nov-Dec;26(6):779-86. doi: 10.2164/jandrol.05069.

Abstract

Previously, we examined the relationship between protamine gene variations and human male infertility. In this study, we show specific variability in the transition nuclear protein genes (TNPs) of sterile male patients. Transition nuclear proteins (TPs) are major nuclear proteins that replace nuclear histones, leading to eventual substitution by protamines during human spermiogenesis. Analysis of the human TNP1 and TNP2 gene sequences in 282 sterile male patients and 270 (TNP1) and 266 (TNP2) proven-fertile male volunteers revealed 5 amino acid substitution-causing single nucleotide polymorphisms (SNPs) in the open-reading frame of the TNP2 gene. On the other hand, a deletion of 15 nucleotides, which encompassed the recognition site for the cAMP response element (CRE) transcription factor, was found in the 5'-promoter region of the TNP1 gene in infertile men. This deletion reduces TNP1 expression and may cause human male infertility.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Chromosomal Proteins, Non-Histone / genetics*
  • DNA Mutational Analysis
  • Fertility / genetics*
  • Gene Frequency
  • Humans
  • Infertility, Male / genetics*
  • Male
  • Molecular Sequence Data
  • Nuclear Proteins / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Single Nucleotide*
  • Protamines / genetics

Substances

  • Chromosomal Proteins, Non-Histone
  • Nuclear Proteins
  • Protamines
  • spermatid transition proteins