Abstract |
Glucagon-like peptide-1 (GLP-1) is a hormone derived from the preproglucagon molecule that is secreted by intestinal L cells and stimulates insulin secretion from beta cells. The GLP-1 receptor is a candidate gene for diabetes mellitus, as mutations may induce the impaired insulin response that is a characteristic feature of NIDDM. To study the relationship between the GLP-1 receptor gene and NIDDM, linkage of a microsatellite polymorphism flanking the GLP-1 receptor gene with diabetes was investigated in three Caucasian families with MODY and in the nuclear families of 12 NIDDM probands. A cumulative LOD score -8.50 excludes linkage in these MODY pedigrees. A LOD score of -1.24 in the NIDDM nuclear pedigrees makes linkage improbable. Mutations in or near the GLP-1 receptor gene are unlikely to be the major cause of the inherited predisposition to NIDDM in Caucasian pedigrees, but we cannot exclude a role for this locus in a polygenic model or a major role in some pedigrees.
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Authors | Y Zhang, J T Cook, A T Hattersley, R Firth, P J Saker, M Warren-Perry, M Stoffel, R C Turner |
Journal | Diabetologia
(Diabetologia)
Vol. 37
Issue 7
Pg. 721-4
(Jul 1994)
ISSN: 0012-186X [Print] Germany |
PMID | 7958545
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- GLP1R protein, human
- Glucagon-Like Peptide-1 Receptor
- Oligonucleotide Probes
- Receptors, Cell Surface
- Receptors, Glucagon
- DNA
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Topics |
- Base Sequence
- DNA
(analysis)
- Diabetes Mellitus, Type 2
(genetics, metabolism)
- Electrophoresis, Polyacrylamide Gel
- Female
- Genes
- Genetic Linkage
- Glucagon-Like Peptide-1 Receptor
- Humans
- Lod Score
- Male
- Molecular Sequence Data
- Oligonucleotide Probes
- Pedigree
- Polymerase Chain Reaction
- Receptors, Cell Surface
(genetics)
- Receptors, Glucagon
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