Molecular identification and characterization of two medium-chain Acyl-CoA synthetases, MACS1 and the Sa gene product

被引:59
作者
Fujino, T
Takei, YA
Sone, H
Ioka, RX
Kamataki, A
Magoori, K
Takahashi, S
Sakai, J
Yamamoto, TT
机构
[1] Tohoku Univ, Ctr Gene Res, Sendai, Miyagi 9818555, Japan
[2] Fukui Med Univ, Dept Internal Med 3, Fukui 9101193, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Med, Div Nephrol Endocrinol & Vasc Med, Sendai, Miyagi 9808574, Japan
关键词
D O I
10.1074/jbc.M106651200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In this study, we identified and characterized two murine cDNAs encoding medium-chain acyl-CoA synthetase (MACS). One, designated MACS1, is a novel protein and the other the product of the Sa gene (Sa protein), which is preferentially expressed in spontaneously hypertensive rats. Based on the murine MACS1 sequence, we also identified the location and organization of the human MACS1 gene, showing that the human MACS1 and Sa genes are located in the opposite transcriptional direction within a 150-kilobase region on chromosome 16p13.1. Murine MACS1 and Sa protein were overexpressed in COS cells, purified to homogeneity, and characterized. Among C4-C16 fatty acids, MACS1 preferentially utilizes octanoate, whereas isobutyrate is the most preferred fatty acid among C2-C6 fatty acids for Sa protein. Like Sa gene transcript, MACS1 mRNA was detected mainly in the liver and kidney. Subcellular fractionation revealed that both MACS1 and Sa protein are localized in the mitochondrial matrix. C-14-Fatty acid incorporation studies indicated that acyl-CoAs produced by MACS1 and Sa protein are utilized mainly for oxidation.
引用
收藏
页码:35961 / 35966
页数:6
相关论文
共 29 条
[1]
[Anonymous], 1983, COLD SPRING HARBOR L
[2]
[Anonymous], 1988, Antibodies: A Laboratory Manual
[3]
Molecular characterization and expression of rat acyl-CoA synthetase 3 [J].
Fujino, T ;
Kang, MJ ;
Suzuki, H ;
Iijima, H ;
Yamamoto, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) :16748-16752
[4]
CLONING AND FUNCTIONAL EXPRESSION OF A NOVEL LONG-CHAIN ACYL-COA SYNTHETASE EXPRESSED IN BRAIN [J].
FUJINO, T ;
YAMAMOTO, T .
JOURNAL OF BIOCHEMISTRY, 1992, 111 (02) :197-203
[5]
Acetyl-CoA synthetase 2, a mitochondrial matrix enzyme involved in the oxidation of acetate [J].
Fujino, T ;
Kondo, J ;
Ishikawa, M ;
Morikawa, K ;
Yamamoto, TT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (14) :11420-11426
[6]
Genome scan and congenic strains for blood pressure QTL using Dahl salt-sensitive rats [J].
Garrett, MR ;
Dene, H ;
Walder, R ;
Zhang, QY ;
Cicila, GT ;
Assadnia, S ;
Deng, AY ;
Rapp, JP .
GENOME RESEARCH, 1998, 8 (07) :711-723
[7]
POSSIBLE ALTERNATIVE SPLICING OF THE RAT SA GENE [J].
GU, L ;
DENE, H ;
RAPP, JP .
MAMMALIAN GENOME, 1995, 6 (09) :683-684
[8]
S(A) GENE AND BLOOD-PRESSURE COSEGREGATION USING DAHL SALT-SENSITIVE RATS [J].
HARRIS, EL ;
DENE, H ;
RAPP, JP .
AMERICAN JOURNAL OF HYPERTENSION, 1993, 6 (04) :330-334
[9]
Molecular cloning of KS, a novel rat gene expressed exclusively in the kidney [J].
Hilgers, KF ;
Nagaraj, SK ;
Karginova, EA ;
Kazakova, IG ;
Chevalier, RL ;
Carey, RM ;
Pentz, ES ;
Gomez, RA .
KIDNEY INTERNATIONAL, 1998, 54 (05) :1444-1454
[10]
Congenic substitution mapping excludes Sa as a candidate gene locus for a blood pressure quantitative trait locus on rat chromosome 1 [J].
Hübner, N ;
Lee, YA ;
Lindpaintner, K ;
Ganten, D ;
Kreutz, R .
HYPERTENSION, 1999, 34 (04) :643-648