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• W2028102364 endingPage "1878" @default.
• W2028102364 startingPage "1871" @default.
• W2028102364 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." @default.
• W2028102364 created "2016-06-24" @default.
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• W2028102364 date "1992-01-01" @default.
• W2028102364 modified "2023-10-15" @default.
• W2028102364 title "<i>Cis</i>-regulation of the L-type pyruvate kinase gene promoter by glucose, insulin and cyclic AMP" @default.
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• W2028102364 doi "https://doi.org/10.1093/nar/20.8.1871" @default.
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