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The tripartite DNA element responsible for diet-induced rat fatty acid synthase (FAS) regulation

  • Karim Roder
  • , Hans Klein
  • , Harald Kranz
  • , Karl-Friedrich Beck
  • , Michael Schweizer*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

We investigated which region of the 5′-flanking sequence of the rat fatty acid synthase (FAS)-encoding gene could be responsible for its nutritionally regulated expression. Diet-induced differences in chromatin structure were determined by DNase I treatment of intact nuclei from hepatic tissue. A low-fat diet results in a different pattern of DNase I-hypersensitive sites (HS) in the chromatin of the FAS promoter (pFAS) from that seen when the nuclear extract was prepared from the livers of normally fed rats. The protein-binding properties of the region defined by DNase I hypersensitivity were tested by gel retardation. A putative cis-acting element with a tripartite structure, 5′-GCCT, 6-bp spacer and a 3′-palindrome, could be localized between bp - 518 to - 495 in pFAS. Competition experiments with oligodeoxyribo-nucleotides (oligos) representing subfragments of this cis-element showed that the requirement for structure is stricter than that for sequence. This element could be one of the termini of the insulin-induced signal cascade.

Original languageEnglish
Pages (from-to)189-195
Number of pages7
JournalGene
Volume144
Issue number2
DOIs
Publication statusPublished - 8 Jul 1994

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • diabetic
  • Dietary effects
  • EMSA gel retardation
  • fatty acid synthase promoter
  • hypersensitive sites
  • insulin cascade

ASJC Scopus subject areas

  • Genetics

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