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Glucose regulates preproinsulin messenger RNA levels in a clonal cell line of simian virus 40-transformed B cells.

Abstract
In HIT-T15 cells grown in the absence of glucose, Northern blot analysis of total RNA revealed a major 0.5 kb preproinsulin (ppI) mRNA transcript which co-migrated with the mature transcript from a human insulinoma. In 4 h tissue cultures, glucose (2-20 mM) stimulated HIT cell ppI mRNA levels in a markedly dose-dependent manner. Glucose-stimulated ppI mRNA was (i) inhibited by actinomycin D, suggesting that regulation may be in part transcriptional, and (ii) potentiated by agents known to activate B cell protein kinases. HIT cells represent a unique model for investigating long term regulation of insulin gene expression and biosynthesis.
AuthorsP Hammonds, P N Schofield, S J Ashcroft
JournalFEBS letters (FEBS Lett) Vol. 213 Issue 1 Pg. 149-54 (Mar 09 1987) ISSN: 0014-5793 [Print] England
PMID3030804 (Publication Type: Journal Article)
Chemical References
  • Insulin
  • Protein Precursors
  • RNA, Messenger
  • Dactinomycin
  • Colforsin
  • preproinsulin
  • Proinsulin
  • Theophylline
  • Protein Kinases
  • Glucose
  • Bombesin
Topics
  • Animals
  • B-Lymphocytes (metabolism)
  • Bombesin (pharmacology)
  • Cell Line
  • Cell Transformation, Viral
  • Clone Cells
  • Colforsin (pharmacology)
  • Cricetinae
  • Dactinomycin (pharmacology)
  • Dose-Response Relationship, Drug
  • Glucose (pharmacology)
  • Insulin
  • Mesocricetus
  • Proinsulin (genetics)
  • Protein Kinases (metabolism)
  • Protein Precursors (genetics)
  • RNA, Messenger (metabolism)
  • Simian virus 40
  • Theophylline (pharmacology)

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