Structure, function, and dietary regulation of Δ6, Δ5, and Δ9 desaturases

被引:860
作者
Nakamura, MT [1 ]
Nara, TY [1 ]
机构
[1] Univ Illinois, Dept Food Sci & Human Nutr, Urbana, IL 61801 USA
关键词
unsaturated fatty acid synthesis; PPAR; SREBP; LXR; ChREBP;
D O I
10.1146/annurev.nutr.24.121803.063211
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Fatty acid desaturases introduce a double bond in a specific position of long-chain fatty acids, and are conserved across kingdoms. Degree of unsaturation of fatty acids affects physical properties of membrane phospholipids and stored triglycerides. In addition, metabolites of polyunsaturated fatty acids are used as signaling molecules in many organisms. Three desaturases, Delta9, Delta6, and Delta5, are present in humans. Delta-9 catalyzes synthesis of monounsaturated fatty acids. Oleic acid, a main product of Delta9 desaturase, is the major fatty acid in mammalian adipose triglycerides, and is also used for phospholipid and cholesteryl ester synthesis. Delta-6 and Delta5 desaturases are required for the synthesis of highly unsaturated fatty acids (HUFAs), which are mainly esterified into phospholipids and contribute to maintaining membrane fluidity. While HUFAs may be required for cold tolerance in plants and fish, the primary role of HUFAs in mammals is cell signaling. Arachidonic acid is required as substrates for eicosanoid synthesis, while docosahexaenoic acid is required in visual and neuronal functions. Desaturases in mammals are regulated at the transcriptional level. Reflecting overlapping functions, three desaturases share a common mechanism of a feedback regulation to maintain products in membrane phospholipids. At the same time, regulation of Delta9 desaturase differs from Delta6 and Delta5 desaturases because its products are incorporated into more diverse lipid groups. Combinations of multiple transcription factors achieve this sophisticated differential regulation.
引用
收藏
页码:345 / 376
页数:32
相关论文
共 201 条
[1]   Molecular cloning and functional characterization of rat Δ-6 fatty acid desaturase [J].
Aki, T ;
Shimada, Y ;
Inagaki, K ;
Higashimoto, H ;
Kawamoto, S ;
Shigeta, S ;
Ono, K ;
Suzuki, O .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 255 (03) :575-579
[2]  
[Anonymous], AM J MED
[3]   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
[4]   Cloning and characterization of the human stearoyl-CoA desaturase gene promoter:: Transcriptional activation by sterol regulatory element binding protein and repression by polyunsaturated fatty acids and cholesterol [J].
Bené, H ;
Lasky, D ;
Ntambi, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 284 (05) :1194-1198
[5]   THE RELATION BETWEEN INSULIN SENSITIVITY AND THE FATTY-ACID COMPOSITION OF SKELETAL-MUSCLE PHOSPHOLIPIDS [J].
BORKMAN, M ;
STORLIEN, LH ;
PAN, DA ;
JENKINS, AB ;
CHISHOLM, DJ ;
CAMPBELL, LV .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (04) :238-244
[6]  
BRIGGS MR, 1993, J BIOL CHEM, V268, P14490
[7]   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
[8]  
BROWSE J, 1993, J BIOL CHEM, V268, P16345
[9]   Nuclear receptors and lipid physiology: Opening the X-files [J].
Chawla, A ;
Repa, JJ ;
Evans, RM ;
Mangelsdorf, DJ .
SCIENCE, 2001, 294 (5548) :1866-1870
[10]   Integrated models of distribution transformers and their loads for three-phase power flow analyses [J].
Chen, TH ;
Chang, YL .
IEEE TRANSACTIONS ON POWER DELIVERY, 1996, 11 (01) :507-513