Activity and genomic organization of human glucose transporter 9 (GLUT9), a novel member of the family of sugar-transport facilitators predominantly expressed in brain and leucocytes

被引:136
作者
Doege, H [1 ]
Bocianski, A [1 ]
Joost, HG [1 ]
Schürmann, A [1 ]
机构
[1] Rhein Westfal TH Aachen, Fak Med, Inst Pharmakol & Toxikol, D-52057 Aachen, Germany
关键词
cytochalasin B binding; glucose-transporter protein; reconstituted glucose-transport activity; sugar transporter signature;
D O I
10.1042/0264-6021:3500771
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
The GLUT9 gene encodes a cDNA which exhibits significant sequence similarity with members of the glucose transporter (GLUT) family. The gene is located on chromosome 9q34 and consists of 10 exons separated by short introns. The amino acid sequence deduced from its cDNA predicts 12 putative membrane-spanning helices and all the motifs (sugar-transporter signatures) that have previously been shown to be essential for transport activity. A striking characteristic of GLUT9 is the presence of two arginines in the putative helices 7 and 8 at positions where the organic anion transporters harbour basic residues. The next relative of GLUT9 is the glucose transporter GLUT8/GLUTX1 (44.8 % amino acid identity with GLUT9). A 2.6-kb transcript of GLUTS, was detected in spleen, peripheral leucocytes and brain. Transfection of COS-7 cells with GLUTS, produced expression of a 46-kDa membrane protein which exhibited reconstitutable glucose-transport activity and low-affinity cytochalasin-B binding. It is concluded that GLUT9 is a novel member of the family of sugar-transport facilitators with a tissue-specific function.
引用
收藏
页码:771 / 776
页数:6
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