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Effects of glucose, insulin, and cAMP on transcription of the serine dehydratase gene in rat liver.

Abstract
Starvation and diabetes both caused a dramatic induction of hepatic L-serine dehydratase (SDH) (EC 4.2.1.13) in rats. Increases in the activity of the enzyme which had been demonstrated in several previous studies were found to be associated with increases in the amount of SDH protein and its mRNA in our studies reported herein. Nuclear run-on experiments with isolated liver nuclei demonstrated that the increases in SDH activity were mainly the result of increases in the rate of SDH gene transcription. Refeeding of glucose to starved rats or the administration of insulin to diabetic rats caused a marked reduction in the amount of SDH mRNA. The rates of transcription as measured in isolated nuclei were reduced to uninduced levels within 30 min of either treatment. Following the administration of Bt2-cAMP, the transcription rates of the SDH gene returned to the original induced rates within 40 min both in glucose-refed rats and in diabetic rats administered insulin. The results of these experiments indicate that the induction of SDH in rat liver in vivo is controlled predominantly at the level of gene transcription by the reciprocal action of cAMP and insulin.
AuthorsR Kanamoto, Y Su, H C Pitot
JournalArchives of biochemistry and biophysics (Arch Biochem Biophys) Vol. 288 Issue 2 Pg. 562-6 (Aug 01 1991) ISSN: 0003-9861 [Print] United States
PMID1654838 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Insulin
  • RNA, Messenger
  • Bucladesine
  • DNA
  • Cyclic AMP
  • Glucose
Topics
  • Animals
  • Bucladesine (pharmacology)
  • Cyclic AMP (physiology)
  • DNA (genetics, isolation & purification)
  • Diabetes Mellitus, Experimental (enzymology, genetics)
  • Glucose (pharmacology)
  • Insulin (pharmacology)
  • Kinetics
  • Liver (drug effects, enzymology)
  • Male
  • RNA, Messenger (drug effects, genetics, metabolism)
  • Rats
  • Rats, Inbred Strains
  • Reference Values
  • Starvation
  • Transcription, Genetic (drug effects)

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