Fatty acid transport by vectorial acylation in mammals: Roles played by different isoforms of rat long-chain acyl-CoA synthetases

被引:43
作者
Tong, FM
Black, PN
Coleman, RA
DiRusso, CC [1 ]
机构
[1] Albany Med Coll, Ctr Metab Dis, Ordway Res Inst, Albany, NY 12208 USA
[2] Albany Med Coll, Ctr Cardiovasc Sci, Albany, NY 12208 USA
[3] Univ N Carolina, Dept Nutr, Chapel Hill, NC 27599 USA
关键词
acyl-CoA synthetase; vectorial acylation; fatty acid transport; rat; yeast; triglyceride synthesis;
D O I
10.1016/j.abb.2006.01.005
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
Mammals express multiple isoforms of acyl-CoA synthetase (ACSL1 and ACSL3-6) in various tissues. These enzymes are essential for fatty acid metabolism providing activated intermediates for complex lipid synthesis, protein modification, and P-oxidation. Yeast in contrast express four major ACSLs, which have well-defined functions. Two, Faa1p and Faa4p, are specifically required for fatty acid transport by vectorial acylation. Four ACSLs from the rat were expressed in a yeast faa1 Delta faa4 Delta strain and their roles in fatty acid transport and trafficking characterized. All four restored ACS activity yet varied in substrate preference. ACSL1, 4, and 6 were able to rescue fatty acid transport activity and triglyceride synthesis. ACSL5, however, was unable to facilitate fatty acid transport despite conferring robust oleoyl-CoA synthetase activity. This is the first study evaluating the role of the mammalian ACSLs in fatty acid transport and supports a role for ACSL1, 4, and 6 in transport by vectorial acylation. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:46 / 52
页数:7
相关论文
共 38 条
[1]   Peroxisome proliferator-activated receptor β regulates acyl-CoA synthetase 2 in reaggregated rat brain cell cultures [J].
Basu-Modak, S ;
Braissant, O ;
Escher, P ;
Desvergne, B ;
Honegger, P ;
Wahli, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (50) :35881-35888
[2]   Affinity labeling fatty acyl-CoA synthetase with 9-p-azidophenoxy nonanoic acid and the identification of the fatty acid-binding site [J].
Black, PN ;
DiRusso, CC ;
Sherin, D ;
MacColl, R ;
Knudsen, J ;
Weimar, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (49) :38547-38553
[3]   Transmembrane movement of exogenous long-chain fatty acids: Proteins, enzymes, and vectorial esterification [J].
Black, PN ;
DiRusso, CC .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (03) :454-+
[4]   Mutational analysis of a fatty acyl-coenzyme A synthetase signature motif identifies seven amino acid residues that modulate fatty acid substrate specificity [J].
Black, PN ;
Zhang, Q ;
Weimar, JD ;
DiRusso, CC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (08) :4896-4903
[5]   Rat long chain acyl-CoA synthetase 5, but not 1, 2, 3, or 4, complements Escherichia coli fadD [J].
Caviglia, JM ;
Li, LO ;
Wang, SL ;
DiRusso, CC ;
Coleman, RA ;
Lewin, TM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (12) :11163-11169
[6]   Do long-chain Acyl-CoA synthetases regulate fatty acid entry into synthetic versus degradative pathways? [J].
Coleman, RA ;
Lewin, TM ;
Van Horn, CG ;
Gonzalez-Baró, MR .
JOURNAL OF NUTRITION, 2002, 132 (08) :2123-2126
[7]   Comparative biochemical studies of the murine fatty acid transport proteins (FATP) expressed in yeast [J].
DiRusso, CC ;
Li, H ;
Darwis, D ;
Watkins, PA ;
Berger, J ;
Black, PN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (17) :16829-16837
[8]  
DIRUSSO CC, 2004, J BIOL CHEM
[9]   ISOLATION OF A SACCHAROMYCES-CEREVISIAE LONG-CHAIN FATTY ACYL-COA SYNTHETASE GENE (FAA1) AND ASSESSMENT OF ITS ROLE IN PROTEIN N-MYRISTOYLATION [J].
DURONIO, RJ ;
KNOLL, LJ ;
GORDON, JI .
JOURNAL OF CELL BIOLOGY, 1992, 117 (03) :515-529
[10]   Disruption of the Saccharomyces cerevisiae homologue to the murine fatty acid transport protein impairs uptake and growth on long-chain fatty acids [J].
Faergeman, NJ ;
DiRusso, CC ;
Elberger, A ;
Knudsen, J ;
Black, PN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (13) :8531-8538