Mechanisms of regulation of gene expression by fatty acids

被引:166
作者
Nakamura, MT
Cheon, Y
Li, Y
Nara, TY
机构
[1] Univ Illinois, Dept Food Sci & Human Nutr, Urbana, IL 61801 USA
[2] Univ Illinois, Div Nutr Sci, Urbana, IL 61801 USA
关键词
D O I
10.1007/s11745-004-1333-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 alpha (PPARalpha), 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 monounsaturated 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. PPARalpha 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 PPARalpha. Dietary PUFA, except for 18:2 n-6, are likely to induce FA oxidation enzymes via PPARalpha as a "feed-forward" mechanism. PPARalpha is also required for regulating the synthesis of highly unsaturated FA, indicating pleiotropic functions of PPARalpha 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.
引用
收藏
页码:1077 / 1083
页数:7
相关论文
共 82 条
[1]   Tissue distribution and quantification of the expression of mRNAs of peroxisome proliferator-activated receptors and liver X receptor-alpha in humans - No alteration in adipose tissue of obese and NIDDM patients [J].
Auboeuf, D ;
Rieusset, J ;
Fajas, L ;
Vallier, P ;
Frering, V ;
Riou, JP ;
Staels, P ;
Auwerx, J ;
Laville, M ;
Vidal, H .
DIABETES, 1997, 46 (08) :1319-1327
[2]   Coordinate induction of peroxisomal acyl-CoA oxidase and UCP-3 by dietary fish oil: a mechanism for decreased body fat deposition [J].
Baillie, RA ;
Takada, R ;
Nakamura, M ;
Clarke, SD .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1999, 60 (5-6) :351-356
[3]  
BRIGGS MR, 1993, J BIOL CHEM, V268, P14490
[4]   The SREBP pathway: Regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor [J].
Brown, MS ;
Goldstein, JL .
CELL, 1997, 89 (03) :331-340
[5]  
Cheon YW, 2004, FASEB J, V18, pA863
[6]   REGULATION OF GENE-TRANSCRIPTION BY POLYUNSATURATED FATTY-ACIDS [J].
CLARKE, SD ;
JUMP, DB .
PROGRESS IN LIPID RESEARCH, 1993, 32 (02) :139-149
[7]  
CLARKE SD, 1994, ANNU REV NUTR, V14, P83, DOI 10.1146/annurev.nu.14.070194.000503
[8]   SPECIFIC INHIBITION OF HEPATIC FATTY-ACID SYNTHESIS EXERTED BY DIETARY LINOLEATE AND LINOLENATE IN ESSENTIAL FATTY-ACID ADEQUATE RATS [J].
CLARKE, SD ;
ROMSOS, DR ;
LEVEILLE, GA .
LIPIDS, 1976, 11 (06) :485-490
[9]   The CYP4A Isoforms hydroxylate epoxyeicosatrienoic acids to form high affinity peroxisome proliferator-activated receptor ligands [J].
Cowart, LA ;
Wei, SZ ;
Hsu, MH ;
Johnson, EF ;
Krishna, MU ;
Falck, JR ;
Capdevila, JH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (38) :35105-35112
[10]   Peroxisome proliferator-activated receptor α is not rate-limiting for the lipoprotein-lowering action of fish oil [J].
Dallongeville, J ;
Baugé, E ;
Tailleux, A ;
Peters, JM ;
Gonzalez, FJ ;
Fruchart, JC ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (07) :4634-4639