Identification of GFAT1-L, a novel splice variant of human glutamine:: fructose-6-phosphate amidotransferase (GFAT1) that is expressed abundantly in skeletal muscle

被引:31
作者
Niimi, M
Ogawara, T
Yamashita, T
Yamamoto, Y
Ueyama, A
Kambe, T
Okamoto, T
Ban, T
Tamanoi, H
Ozaki, K
Fujiwara, T
Fukui, H
Takahashi, E
Kyushiki, H
Tanigami, A
机构
[1] Otsuka Pharmaceut Co Ltd, Otsuka GEN Res Inst, Tokushima 7710192, Japan
[2] Otsuka Pharmaceut Co Ltd, Inst New Drug Res 1, Tokushima 7710192, Japan
[3] Otsuka Pharmaceut Co Ltd, Ako Res Inst, Tokushima 7710192, Japan
[4] Univ Tokushima, Fac Pharmaceut Sci, Dept Pharmacol, Tokushima 770, Japan
关键词
GFAT1; NIDDM; insulin resistance; skeletal muscle; tissue-specific gene;
D O I
10.1007/s100380170022
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Glutamine:fructose-6-phosphate amidotransferase (GFAT1) is the rate-limiting enzyme in the hexosamine biosynthetic pathway, which plays an important role in hyperglycemia-induced insulin resistance. To evaluate the role of GFAT1 expression, we analyzed the expression profiles of GFAT1 mRNA in various human tissues using reverse transcriptase-polymerase chain reaction. We report here the identification and cDNA cloning of a novel GFAT1splice variant expressed abundantly in skeletal muscle and heart. This subtype, designated GFAT1-L, contains a 54-bp insertion within the GFAT1coding sequence. Recombinant GFAT1-L protein possessed functional GFAT activities and biochemical characteristics similar to GFAT1. Previously, GFAT1 was considered a simplex enzyme. The identification of a novel GFAT1 subtype possessing functional enzymatic activity and tissue-specific expression should provide additional insight into the mechanism of skeletal muscle insulin resistance and diabetes complications.
引用
收藏
页码:566 / 571
页数:6
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