Molecular cloning of a novel member of the GLUT family of transporters, SLC2A10 (GLUT10), localized on chromosome 20q13.1: A candidate gene for NIDDM susceptibility

被引:118
作者
McVie-Wylie, AJ [1 ]
Lamson, DR [1 ]
Chen, YT [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Pediat, Div Med Genet, Durham, NC 27710 USA
关键词
D O I
10.1006/geno.2000.6457
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Non-insulin-dependent diabetes mellitus (NIDDM) is a multifactoral disease with both environmental and genetics causes. Genome-wide screening procedures have identified several susceptibility loci for NIDDM within the human genome. We describe the cloning of a putative sugar transporter that has been localized to human chromosome 20q12-q13.1, one of the genomic loci associated with NIDDM. Because of the strong resemblance of this novel protein to members of the mammalian facilitative glucose transporter family (GLUT), we refer to the protein as GLUT10 (HGMW-approved gene symbol SLC2A10). GLUT10 contains 541 amino acids with several glucose transporter sequence motifs and amino acids essential for glucose transport function. In addition, secondary structure analysis of GLUT10 predicts 12 putative transmembrane domains, a hallmark structure of the GLUT family. The tissue distribution of GLUT10 was determined by Northern analysis, which revealed highest levels of expression in the liver and pancreas. From these data, we believe that the chromosomal localization, tissue distribution, and predicted function make GLUT10 an excellent candidate for a susceptibility gene involved in NIDDM. (C) 2001 Academic Press.
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页码:113 / 117
页数:5
相关论文
共 17 条
[1]   Structure and function of facilitative sugar transporters [J].
Barrett, MP ;
Walmsley, AR ;
Gould, GW .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (04) :496-502
[2]   Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy [J].
Bowden, DW ;
Sale, M ;
Howard, TD ;
Qadri, A ;
Spray, BJ ;
Rothschild, CB ;
Akots, G ;
Rich, SS ;
Freedman, BI .
DIABETES, 1997, 46 (05) :882-886
[3]   Glucose transporters: Structure, function and consequences of deficiency [J].
Brown, GK .
JOURNAL OF INHERITED METABOLIC DISEASE, 2000, 23 (03) :237-246
[4]   Liver hyperplasia and paradoxical regulation of glycogen metabolism and glucose-sensitive gene expression in GLUT2-null hepatocytes -: Further evidence for the existence of a membrane-based glucose release pathway [J].
Burcelin, R ;
Muñoz, MD ;
Guillam, MT ;
Thorens, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) :10930-10936
[5]   Type 2 diabetes: Evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs [J].
Ghosh, S ;
Watanabe, RM ;
Hauser, ER ;
Valle, T ;
Magnuson, VL ;
Erdos, MR ;
Langefeld, CD ;
Balow, J ;
Ally, DS ;
Kohtamaki, K ;
Chines, P ;
Birznieks, G ;
Kaleta, HS ;
Musick, A ;
Te, C ;
Tannenbaum, J ;
Eldridge, W ;
Shapiro, S ;
Martin, C ;
Witt, A ;
So, A ;
Chang, J ;
Shurtleff, B ;
Porter, R ;
Kudelko, K ;
Unni, A ;
Segal, L ;
Sharaf, R ;
Blaschak-Harvan, J ;
Eriksson, J ;
Tenkula, T ;
Vidgren, G ;
Ehnholm, C ;
Tuomilehto-Wolf, E ;
Hagopian, W ;
Buchanan, TA ;
Tuomilehto, J ;
Bergman, RN ;
Collins, FS ;
Boehnke, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2198-2203
[6]   Normal hepatic glucose production in the absence of GLUT2 reveals an alternative pathway for glucose release from hepatocytes [J].
Guillam, MT ;
Burcelin, R ;
Thorens, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (21) :12317-12321
[7]   MOLECULAR PHYSIOLOGY OF SODIUM-GLUCOSE COTRANSPORTERS [J].
HEDIGER, MA ;
RHOADS, DB .
PHYSIOLOGICAL REVIEWS, 1994, 74 (04) :993-1026
[8]   GLUTX1, a novel mammalian glucose transporter expressed in the central nervous system and insulin-sensitive tissues [J].
Ibberson, M ;
Uldry, M ;
Thorens, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (07) :4607-4612
[9]   New susceptibility locus for NIDDM is localized to human chromosome 20q [J].
Ji, LN ;
Malecki, M ;
Warram, JH ;
Yang, YD ;
Rich, SS ;
Krolewski, AS .
DIABETES, 1997, 46 (05) :876-881
[10]   INSULIN ACTION, DIABETOGENES, AND THE CAUSE OF TYPE-II DIABETES [J].
KAHN, CR .
DIABETES, 1994, 43 (08) :1066-1084