Promoter analysis of the Drosophila genes encoding TFIIB and TATA box-binding protein

Mol Cells. 1998 Dec 31;8(6):770-6.

Abstract

We have analyzed the 5'-flanking regions of the Drosophila genes encoding the TFIIB and TATA box-binding proteins (TBP) and mapped the regulatory regions required for their efficient expression. We found that the 500 bp long region (-439 to +60) and the 401 bp long region (-261 to +138) are required for the efficient expression of TFIIB and TBP genes, respectively. In the TFIIB promoter region, the upstream DNA between -439 and -280 and the downstream DNA between +8 and +60 are necessary for the stimulation of promoter activity. The upstream DNA between -439 and -280 stimulates transcription in an orientation dependent manner. In the TBP promoter region, the upstream DNA between -261 and -207, and the downstream DNA between +15 and +138 are necessary for the stimulation of promoter activity. The upstream DNA (-261 to -207) required for TBP promoter activity contains a 11 bp long palindromic sequence and a DNA replication-related element sequence. Particularly, we could find that the downstream promoter regions of TFIIB and TBP genes contain the conserved nucleotide sequences, suggesting the presence of a common regulatory mechanism for the expression of these two genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • DNA / genetics
  • DNA-Binding Proteins / genetics*
  • Drosophila / cytology
  • Drosophila / genetics*
  • Genes, Insect / genetics*
  • Luciferases / genetics
  • Luciferases / metabolism
  • Promoter Regions, Genetic / genetics*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Sequence Deletion
  • Sequence Homology, Nucleic Acid
  • TATA Box
  • TATA-Box Binding Protein
  • Transcription Factor TFIIB
  • Transcription Factors / genetics*

Substances

  • DNA-Binding Proteins
  • Recombinant Fusion Proteins
  • TATA-Box Binding Protein
  • Transcription Factor TFIIB
  • Transcription Factors
  • DNA
  • Luciferases