In vivo activity of the most proximal promoter of the human aldolase A gene and analysis of transcriptional control elements

FEBS Lett. 1989 Oct 23;257(1):75-80. doi: 10.1016/0014-5793(89)81790-9.

Abstract

The genomic region upstream from exon F (exon IV) of the human aldolase A gene has been studied for its ability to direct the transcription of a reporter gene in vivo. Transfection experiments in human hepatoma cells (Hep 3B) followed by CAT assay, and S1 mapping analysis, demonstrated that: (i) this region is able to drive CAT gene transcription; (ii) all the transcriptional control elements of this promoter are downstream from nucleotide -384 of the longer ubiquitous RNA start site and the sequences between -384 and -262 play a crucial role in transcriptional efficiency; (iii) initiation starting points for two mRNAs exist 61 bp apart. Gel retardation and footprinting assays demonstrated the presence of DNA-protein complexes mainly in the region between -384 and -262 and such ubiquitous binding factors as Sp1 and AP-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Carcinoma, Hepatocellular
  • Cell Line
  • Chloramphenicol O-Acetyltransferase / genetics
  • Chromosome Deletion
  • Deoxyribonuclease I
  • Exons
  • Fructose-Bisphosphate Aldolase / genetics*
  • Genes*
  • HeLa Cells / metabolism
  • Humans
  • Liver Neoplasms
  • Molecular Sequence Data
  • Nuclear Proteins / metabolism
  • Plasmids
  • Promoter Regions, Genetic*
  • Restriction Mapping
  • Transcription, Genetic*
  • Transfection

Substances

  • Nuclear Proteins
  • Chloramphenicol O-Acetyltransferase
  • Deoxyribonuclease I
  • Fructose-Bisphosphate Aldolase