Marie-Pierre Simon

Cyclic AMP as a transcriptional inhibitor of upper eukaryotic gene transcription

Recently, glucagon and its second messenger, cyclic AMP, have been shown to stimulate the transcription rate of several upper eukaryotic genes (1-5). We show here that glucagon can also block gene transcription. Both glucagon and cyclic AMP were found to inhibit the transcription of the genes encoding three liver glycolytic enzymes, including L-type pyruvate kinase and aldolase B. Thus, cyclic AMP proves to be not only an activator but also an inhibitor of gene transcription in eukaryotes.

Cotranslation of L and L′ pyruvate kinase messenger RNAs from human fetal liver

Abstract Human fetal liver RNA translated in a rabbit reticulocyte cell-free system directed synthesis of two polypeptides which could be identified by immunological competition as L and L′ pyruvate kinase subunits. Messenger RNAs specifying synthesis of both types of subunits exhibited a sedimentation coefficient of 21–22 S.