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Appearance of a nonfunctional isozyme of hepatic glycogen synthase in late gestation.
Hsu, S D; Jaspers, S R; Davis, B B; Cardell, R R; Miller, T B; Drake, R L.
Afiliação
  • Hsu SD; Department of Anatomy and Cell Biology, University of Cincinnati, Ohio.
Arch Biochem Biophys ; 281(1): 152-6, 1990 Aug 15.
Article em En | MEDLINE | ID: mdl-2116768
ABSTRACT
Glycogen levels, glycogen synthase activities, and glycogen synthase protein levels were determined in liver tissues obtained from 14- to 19-day-old fetal mice, newborn mice, and adult mice. The results of these experiments demonstrate a significant increase in the quantity of hepatic glycogen synthase beginning at Day 17 of gestation and reaching adult levels at birth. However, during the same time period, there is a dramatic decrease in total glycogen synthase activity suggesting that the accumulating glycogen synthase molecules are unable to transfer UDP-glucose to glycogen. These inversely coordinated changes in the quantity and activity of glycogen synthase are consistent with the suggestion that glycogen synthesis in the near-term fetal mouse is being maintained by preexisting enzyme, while accumulating enzyme molecules may represent a quiescent isozyme.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicogênio Sintase / Isoenzimas / Fígado Limite: Animals / Pregnancy Idioma: En Revista: Arch Biochem Biophys Ano de publicação: 1990 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicogênio Sintase / Isoenzimas / Fígado Limite: Animals / Pregnancy Idioma: En Revista: Arch Biochem Biophys Ano de publicação: 1990 Tipo de documento: Article