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Nucleic Acids Res. 1992 Apr 25;20(8):1871-7.

Cis-regulation of the L-type pyruvate kinase gene promoter by glucose, insulin and cyclic AMP.

Author information

  • 1ICGM, Laboratoire de recherches en Génétique et pathologie Moléculaire, INSERM U.129, CHU Cochin, Paris, France.

Abstract

The glucose/insulin response element of the L-pyruvate kinase gene is a perfect palindrome located from nt -168 to -144 with respect to the cap site. This element (L4) is partially homologous to MLTF binding sites. Its full efficiency requires cooperation with a contiguous binding site for HNF4, termed L3 and located from nt -145 to -125. In the presence of the L4 element contiguous to L3, cyclic AMP inhibits activity of the L-PK promoter while in its absence, or when the normal L4-L3 contiguity is modified, cyclic AMP behaves as a transcriptional activator that does not seem to be sequence-specific. Therefore, we propose that the mechanism of inhibition of the L-PK gene by cyclic AMP requires precise interactions between the nucleoprotein complex built up at sites L4 and L3 and other components of the L-PK transcription initiation complex.

PMID:
1315961
[PubMed - indexed for MEDLINE]
PMCID:
PMC312300
Free PMC Article
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