Mechanisms of regulation of gene expression by fatty acids

Manabu T. Nakamura, Yewon Cheon, Yue Li, Takayuki Y. Nara

Research output: Contribution to journalArticlepeer-review

Abstract

Fatty acids (FA) regulate the expression of genes involved in lipid and energy metabolism. In particular, two transcription factors, sterol regulatory element binding protein-1c (SREBP-1c) and peroxisome proliferator activated receptor α (PPARα), have emerged as key mediators of gene regulation by FA. SREBP-1c induces a set of lipogenic enzymes in liver. Polyunsaturated fatty acids (PUFA), but not saturated or mono-unsaturated FA, suppress the induction of lipogenic genes by inhibiting the expression and processing of SREBP-1c. This unique effect of PUFA suggests that SREBP-1c may regulate the synthesis of unsaturated FA for incorporation into glycerolipids and cholesteryl esters. PPARα plays an essential role in metabolic adaptation to fasting by inducing the genes for mitochondrial and peroxisomal FA oxidation as well as those for ketogenesis in mitochondria. FA released from adipose tissue during fasting are considered as ligands of PPARα. Dietary PUFA, except for 18:2 n-6, are likely to induce FA oxidation enzymes via PPARα as a "feed-forward" mechanism. PPARα is also required for regulating the synthesis of highly unsaturated FA, indicating pleiotropic functions of PPARα in the regulation of lipid metabolic pathways. It is yet to be determined whether FA regulate other transcription factors such as liver-X receptor, hepatocyte nuclear factor 4, and carbohydrate response element binding protein.

Original languageEnglish (US)
Pages (from-to)1077-1083
Number of pages7
JournalLipids
Volume39
Issue number11
DOIs
StatePublished - Nov 2004

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Cell Biology

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