The cloned promoter of the human DNA β-polymerase gene contains a cAMP response element functional in HeLa cells

Ella Englander, S. H. Wilson

Research output: Contribution to journalArticle

13 Scopus citations

Abstract

The mammalian DNA β-polymerase (β-pol) gene is constitutively expressed in cultured cells as a function of growth stage and DNA replication, but is expressed in rodents in a tissue-specific fashion. As revealed by transient expression experiments with wild-type and mutated β-pol promoter fusion genes, the cloned human β-pol promoter is transcriptionally regulated by signals acting through the single palindromic sequence (GT-GACGTCAC) known as an ATF/CRE-binding site centered at position -45 in the core promoter. Although the mere presence of the ATF/CRE palindromic sequence in a promoter does not always confer cAMP responsiveness or protein binding over and around the ATF/CRE sequence, we find that agents that increase cAMP levels (forskolin and IBMX) in HeLa cells activate the β-pol promoter; activation also can be observed by coexpression of the protein kinase A catalytic subunit. Experiments with mutagenized β-pol promoters indicate that the ATF/CRE-binding site mediates these effects. Thus, the ATF/CRE-binding site in the context of this TATA-less constitutive promoter is able to respond to the kinase A signal transduction pathway.

Original languageEnglish (US)
Pages (from-to)61-69
Number of pages9
JournalDNA and Cell Biology
Volume11
Issue number1
StatePublished - 1992
Externally publishedYes

    Fingerprint

ASJC Scopus subject areas

  • Cell Biology
  • Genetics
  • Molecular Biology

Cite this