Purification and characterization of a protein binding to the SP6 kappa promoter. A potential role for CArG-box binding factor-A in kappa transcription

J Biol Chem. 1998 Jul 24;273(30):18881-90. doi: 10.1074/jbc.273.30.18881.

Abstract

A protein interacting with an A-T-rich region that is a positive control element within the SP6 kappa promoter was purified and identified as CArG-box binding factor-A. The purified protein was shown to interact specifically with the coding strand of single-stranded DNA and, with lower affinity, with double-stranded DNA. A mutation that inhibited binding of the protein to the A-T-rich region also aborted the transcriptional stimulatory effect of the region. Two Ets proteins, PU.1 and elf-1, that have previously been shown to bind to an adjacent DNA element were shown to physically interact with CArG-box binding factor-A. An antiserum raised against the protein recognized two different forms indicating either that different splice-forms of CArG-box binding factor-A are expressed, or that the protein is subject to post-translational modification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • Animals
  • Base Sequence
  • DNA / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / isolation & purification*
  • DNA-Binding Proteins / metabolism
  • DNA-Directed RNA Polymerases / metabolism*
  • Immunoglobulin kappa-Chains / genetics*
  • Molecular Sequence Data
  • Promoter Regions, Genetic*
  • Protein Binding
  • Repressor Proteins / genetics
  • Repressor Proteins / isolation & purification*
  • Repressor Proteins / metabolism
  • Transcription Factors / metabolism
  • Tumor Cells, Cultured

Substances

  • DNA-Binding Proteins
  • Immunoglobulin kappa-Chains
  • Repressor Proteins
  • Transcription Factors
  • DNA
  • RNA polymerase SP6
  • DNA-Directed RNA Polymerases