Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1994-5-24
|
| pubmed:abstractText |
The glucokinase locus has been implicated by linkage studies in several Caucasian pedigrees with early onset, autosomal dominant diabetes, and mutations have been identified in a large number of these pedigrees. Although mutations have been reported in some pedigrees with late onset Type 2 (non-insulin-dependent) diabetes mellitus, linkage studies of typical familial Type 2 diabetes did not suggest a major role for this locus. Nonetheless, linkage studies were consistent with the hypothesis that mutations of the glucokinase gene were responsible for the pathogenesis of Type 2 diabetes in a minority of pedigrees or one gene in a polygenic disorder. To systematically address this hypothesis, we examined 60 diabetic members of 18 pedigrees ascertained for two or more Type 2 diabetic siblings and eight unrelated diabetic spouses. Initially, the coding regions from each of the 11 glucokinase exons were examined by the sensitive technique of single strand conformation polymorphism analysis to screen for single nucleotide substitutions. Subsequently, we also sequenced each exon from an affected member of the single pedigree in which a glucokinase allele was most likely to segregate with diabetes. Single strand conformation polymorphism analysis detected only three variants, none of which altered the amino acid sequence. No coding or splice site mutations were detected. Likewise, no additional mutations were detected upon direct sequence analysis. However, additional screening of promoter and 3' untranslated regions detected a variant pattern in the untranslated region of exon 10 which appeared to segregate with diabetes and impaired glucose tolerance in one pedigree.(ABSTRACT TRUNCATED AT 250 WORDS)
|
| pubmed:grant | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0012-186X
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
37
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| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
182-7
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| pubmed:dateRevised |
2010-11-18
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| pubmed:meshHeading |
pubmed-meshheading:8163053-Adult,
pubmed-meshheading:8163053-Base Sequence,
pubmed-meshheading:8163053-DNA,
pubmed-meshheading:8163053-DNA Primers,
pubmed-meshheading:8163053-Diabetes Mellitus, Type 2,
pubmed-meshheading:8163053-European Continental Ancestry Group,
pubmed-meshheading:8163053-Exons,
pubmed-meshheading:8163053-Family,
pubmed-meshheading:8163053-Female,
pubmed-meshheading:8163053-Genetic Linkage,
pubmed-meshheading:8163053-Glucokinase,
pubmed-meshheading:8163053-Humans,
pubmed-meshheading:8163053-Islets of Langerhans,
pubmed-meshheading:8163053-Liver,
pubmed-meshheading:8163053-Male,
pubmed-meshheading:8163053-Molecular Sequence Data,
pubmed-meshheading:8163053-Pedigree,
pubmed-meshheading:8163053-Polymerase Chain Reaction,
pubmed-meshheading:8163053-Polymorphism, Genetic,
pubmed-meshheading:8163053-Sequence Deletion
|
| pubmed:year |
1994
|
| pubmed:articleTitle |
Molecular screening of the glucokinase gene in familial type 2 (non-insulin-dependent) diabetes mellitus.
|
| pubmed:affiliation |
Division of Endocrinology and Metabolism, Veterans Affairs Medical Center, Salt Lake City, UT 84148.
|
| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
|