HSF2BP represses BNC1 transcriptional activity by sequestering BNC1 to the cytoplasm

FEBS Lett. 2013 Jul 11;587(14):2099-104. doi: 10.1016/j.febslet.2013.04.049. Epub 2013 May 23.

Abstract

Basonuclin (BNC1), a zinc finger transcriptional factor, is essential for mouse spermatogenesis. However, the regulatory mechanisms of BNC1 in spermatogenesis are poorly understood. In this study, we identified HSF2BP, a testis-specific binding protein of HSF2, as a binding partner of BNC1 by using yeast two-hybrid screening. HSF2BP could interact with and inhibit BNC1 transcriptional activity without affecting its expression level. Moreover, coexpression of HSF2BP with BNC1 resulted in a striking redistribution of BNC1 to the cytoplasm. These data suggest that HSF2BP may play a pivotal role in regulating BNC1 transcriptional activity and subcellular localization during spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / chemistry
  • Carrier Proteins / physiology*
  • Cytoplasm / metabolism*
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / metabolism*
  • Gene Expression
  • Gene Expression Regulation
  • HEK293 Cells
  • Heat-Shock Proteins
  • Humans
  • Male
  • Mice
  • Mice, Inbred ICR
  • Protein Interaction Domains and Motifs
  • Protein Transport
  • Spermatogenesis
  • Testis / metabolism
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism*
  • Transcription, Genetic*

Substances

  • Bnc1 protein, mouse
  • Carrier Proteins
  • DNA-Binding Proteins
  • HSF2BP protein, mouse
  • Heat-Shock Proteins
  • Transcription Factors