Molecular cloning of a novel 120-kDa TBP-interacting protein

Biochem Biophys Res Commun. 1996 Dec 13;229(2):612-7. doi: 10.1006/bbrc.1996.1852.

Abstract

TATA-binding protein (TBP) is a central component for transcriptional regulation and is a target for various transcription regulators. Using histidine-tagged TBP as a ligand for affinity-purification of proteins bound to TBP, we purified a 120-kD protein, termed TBP-interacting protein 120 (TIP120), from rat liver nuclear extracts. The entire cDNA sequence of TIP120 contained an open reading frame encoding a novel polypeptide of 1230 amino acids. The recombinant TIP120 interacted directly with TBP under a physiological condition in vitro. Immunoprecipitation analysis indicated that TIP120 was associated with TBP in nuclear extracts. Interestingly, the N-terminal region of TIP120 exhibited sequence similarity to that of Drosophila TAF80, which was shown to bind directly to TBP. This novel TBP-binding protein is considered to participate in transcription regulation through the interaction with TBP.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Nucleus / metabolism
  • Cloning, Molecular
  • DNA, Complementary
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Escherichia coli / genetics
  • Liver / metabolism
  • Molecular Sequence Data
  • Protein Binding
  • Rats
  • Sequence Homology, Amino Acid
  • TATA-Box Binding Protein
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • Cand1 protein, rat
  • DNA, Complementary
  • DNA-Binding Proteins
  • TATA-Box Binding Protein
  • Transcription Factors

Associated data

  • GENBANK/D87671