p53 Protein interacts specifically with the meiosis-specific mammalian RecA-like protein DMC1 in meiosis

Carcinogenesis. 2004 Jun;25(6):889-93. doi: 10.1093/carcin/bgh099. Epub 2004 Feb 4.

Abstract

The tumor suppressor protein p53 is specifically expressed during meiosis in spermatocytes. Subsets of p53 knockout mice exhibit testicular giant cell degenerative syndrome, which suggests p53 may be associated with meiotic cell cycle and/or DNA metabolism. Here, we show that p53 binds to the mouse meiosis-specific RecA-like protein Mus musculus DMC1 (MmDMC1). The C-terminal domain (amino acid 234-340) of MmDMC1 binds to DNA-binding domain of p53 protein. p53 might be involved in homologous recombination and/or checkpoint function by directly binding to DMC1 protein to repress genomic instability in meiotic germ cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Adenosine Triphosphatases / physiology
  • Animals
  • Base Sequence
  • Cell Cycle Proteins / metabolism*
  • Cell Cycle Proteins / physiology
  • Cell Line
  • DNA Primers
  • DNA Repair
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology
  • Humans
  • Meiosis / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Nuclear Proteins
  • Phosphate-Binding Proteins
  • Protein Binding
  • Tumor Suppressor Protein p53 / metabolism*
  • Tumor Suppressor Protein p53 / physiology

Substances

  • Cell Cycle Proteins
  • DNA Primers
  • DNA-Binding Proteins
  • Dmc1 protein, mouse
  • Nuclear Proteins
  • Phosphate-Binding Proteins
  • Tumor Suppressor Protein p53
  • Adenosine Triphosphatases
  • DMC1 protein, human