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Microsatellite Polymorphisms at the Glucokinase Locus: a Population Association Study in Caucasian Type 2 Diabetic Subjects

Microsatellite Polymorphisms at the Glucokinase Locus: a Population Association Study in Caucasian Type 2 Diabetic Subjects
Microsatellite Polymorphisms at the Glucokinase Locus: a Population Association Study in Caucasian Type 2 Diabetic Subjects

Glucokinase has a central role in glucose metabolism in pancreatic beta cells and hepatocytes and is an important candidate gene for Type 2 diabetes. Mutations of the glucokinase gene have been reported in Caucasian pedigrees with maturity‐onset diabetes of the young and late‐onset Type 2 diabetes. In population studies of American Blacks and Mauritian Creoles an association between alleles of a glucokinase polymorphism and Type 2 diabetes has been described. Two microsatellite polymorphisms (GCK 1 and GCK 2) flanking the glucokinase gene were investigated in Caucasian subjects. There was no significant linkage disequilibrium between the alleles of the two polymorphisms. The overall allelic frequencies for GCK 1 and the combined haplotypes did not significantly differ between 95 Type 2 diabetic and 76 normoglycaemic subjects. In an expanded cohort of 151 diabetic subjects the allelic frequencies at GCK 2 were also similar to controls. These results suggest that a single mutation of the glucokinase gene is not a common cause of Type 2 diabetes in English Caucasians. 1993 Diabetes UK

Caucasian, Glucokinase, Linkage disequilibrium, Population association, Type 2 diabetes
0742-3071
694-698
Hattersley, A. T.
27a38224-13bf-4e48-98d2-8e31e017a986
Saker, P. J.
4e3cb443-3b25-4b64-aae7-b5462b4c2564
Cook, J. T.E.
3ab1d7d4-765c-4b67-92fa-aaa73252c3bd
Stratton, I. M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Patel, P.
fb6d4749-ff22-420b-a1fa-b6a6fcaabad8
Permutt, M. A.
e17df536-fd5f-4eda-a9a3-1b54acbc1c52
Turner, R. C.
9c4a3b92-5186-43ae-b750-08990e742e4e
Wainscoat, J. S.
3d7adeac-5f52-4b87-9f05-66581877de44
Hattersley, A. T.
27a38224-13bf-4e48-98d2-8e31e017a986
Saker, P. J.
4e3cb443-3b25-4b64-aae7-b5462b4c2564
Cook, J. T.E.
3ab1d7d4-765c-4b67-92fa-aaa73252c3bd
Stratton, I. M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Patel, P.
fb6d4749-ff22-420b-a1fa-b6a6fcaabad8
Permutt, M. A.
e17df536-fd5f-4eda-a9a3-1b54acbc1c52
Turner, R. C.
9c4a3b92-5186-43ae-b750-08990e742e4e
Wainscoat, J. S.
3d7adeac-5f52-4b87-9f05-66581877de44

Hattersley, A. T., Saker, P. J., Cook, J. T.E., Stratton, I. M., Patel, P., Permutt, M. A., Turner, R. C. and Wainscoat, J. S. (1993) Microsatellite Polymorphisms at the Glucokinase Locus: a Population Association Study in Caucasian Type 2 Diabetic Subjects. Diabetic Medicine, 10 (8), 694-698. (doi:10.1111/j.1464-5491.1993.tb00150.x).

Record type: Article

Abstract

Glucokinase has a central role in glucose metabolism in pancreatic beta cells and hepatocytes and is an important candidate gene for Type 2 diabetes. Mutations of the glucokinase gene have been reported in Caucasian pedigrees with maturity‐onset diabetes of the young and late‐onset Type 2 diabetes. In population studies of American Blacks and Mauritian Creoles an association between alleles of a glucokinase polymorphism and Type 2 diabetes has been described. Two microsatellite polymorphisms (GCK 1 and GCK 2) flanking the glucokinase gene were investigated in Caucasian subjects. There was no significant linkage disequilibrium between the alleles of the two polymorphisms. The overall allelic frequencies for GCK 1 and the combined haplotypes did not significantly differ between 95 Type 2 diabetic and 76 normoglycaemic subjects. In an expanded cohort of 151 diabetic subjects the allelic frequencies at GCK 2 were also similar to controls. These results suggest that a single mutation of the glucokinase gene is not a common cause of Type 2 diabetes in English Caucasians. 1993 Diabetes UK

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More information

Published date: October 1993
Keywords: Caucasian, Glucokinase, Linkage disequilibrium, Population association, Type 2 diabetes

Identifiers

Local EPrints ID: 486942
URI: http://eprints.soton.ac.uk/id/eprint/486942
ISSN: 0742-3071
PURE UUID: bf9cb8ff-794c-4b31-b117-ec47314872ae
ORCID for I. M. Stratton: ORCID iD orcid.org/0000-0003-1172-7865

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Date deposited: 08 Feb 2024 17:45
Last modified: 18 Mar 2024 04:01

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Contributors

Author: A. T. Hattersley
Author: P. J. Saker
Author: J. T.E. Cook
Author: I. M. Stratton ORCID iD
Author: P. Patel
Author: M. A. Permutt
Author: R. C. Turner
Author: J. S. Wainscoat

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