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Effects of altered [ADP-ribose]n metabolism on expression of fetal functions by adult hepatocytes

Abstract

The nuclear enzyme ADP-ribosyltransferase (ADPRT) catalyses the postsynthetic modification of chromatin proteins1. The significance of [ADP-ribose]n-modified chromatin proteins for the regulation of chromatin function is not understood1. Recently, [ADP-ribose]n biosynthesis has been demonstrated to participate in the repair of some types of DNA damage2–4. Here we demonstrate that another function of [ADP-ribose]n biosynthesis is related to the regulation of the expression of two fetal functions of cultured hepatocytes—the K-type (III) isozyme of pyruvate kinase, and γ-glutamyltranspeptidase, which is also a marker of early neoplastic transformation of liver cells5.

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Althaus, F., Lawrence, S., He, YZ. et al. Effects of altered [ADP-ribose]n metabolism on expression of fetal functions by adult hepatocytes. Nature 300, 366–368 (1982). https://doi.org/10.1038/300366a0

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