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 language | English |
|---|---|
| Pages (from-to) | 189-195 |
| Number of pages | 7 |
| Journal | Gene |
| Volume | 144 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 8 Jul 1994 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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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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