Rat sn-glycerol-3-phosphate acyltransferase:: molecular cloning and characterization of the cDNA and expressed protein

被引:49
作者
Bhat, BG
Wang, P
Kim, JH
Black, TM
Lewin, TM
Fiedorek, FT
Coleman, RA
机构
[1] Univ N Carolina, Dept Nutr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Pediat, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 1999年 / 1439卷 / 03期
关键词
glycerol-3-phosphate acyltransferase; diacylglycerol metabolism; glycerolipid synthesis; triacylglycerol;
D O I
10.1016/S1388-1981(99)00103-1
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
Rat mitochondrial glycerol-3-phosphate acyltransferase (GPAT) cDNA was cloned and characterized. We identified a cDNA containing an open reading frame of 828 amino acids that had an 89% homology with the coding region of the previously characterized mouse mitochondrial GPAT and a predicted amino acid sequence that was 96% identical. The rat 5' UTR was only 159 nucleotides, in contrast to the 926 nucleotide 5' UTR of the mouse cDNA and had an internal deletion of 167 nucleotides. GPAT was expressed in Sf21 insect cells, and specific inhibitors strongly suggest that, like the Escherichia coli GPAT, the recombinant mitochondrial GPAT and the mitochondrial GPAT isoform in rat liver contain critical serine, histidine, and arginine residues. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:415 / 423
页数:9
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