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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1998-9-17
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pubmed:abstractText |
Three further patients with mutations in the codon for arginine 302 of the E1alpha subunit of the pyruvate dehydrogenase complex have been identified. Mutations in this codon have now been found in nine patients with pyruvate dehydrogenase deficiency in seven unrelated families, in sharp contrast to the great majority of other PDH E1alpha mutations which have been described in single individuals only. Because of the relatively high frequency of this mutation and because very few PDH E1alpha mutations have been demonstrated to be causative, we have established a system for analysing the consequences of defined mutations using transfection of normal and mutant PDH E1alpha cDNA into transformed human fibroblasts which have no endogenous E1alpha mRNA or protein. Using this test system, we have demonstrated that the R302C mutation results in the production of PDH E1alpha protein which is devoid of enzymic activity.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1059-7794
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
114-21
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pubmed:dateRevised |
2009-9-29
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pubmed:meshHeading |
pubmed-meshheading:9671272-Arginine,
pubmed-meshheading:9671272-Blotting, Northern,
pubmed-meshheading:9671272-Blotting, Western,
pubmed-meshheading:9671272-Cell Line, Transformed,
pubmed-meshheading:9671272-Clinical Enzyme Tests,
pubmed-meshheading:9671272-Female,
pubmed-meshheading:9671272-Fibroblasts,
pubmed-meshheading:9671272-Humans,
pubmed-meshheading:9671272-Immunohistochemistry,
pubmed-meshheading:9671272-Infant, Newborn,
pubmed-meshheading:9671272-Nucleotide Mapping,
pubmed-meshheading:9671272-Point Mutation,
pubmed-meshheading:9671272-Pyruvate Dehydrogenase (Lipoamide),
pubmed-meshheading:9671272-Pyruvate Dehydrogenase Complex,
pubmed-meshheading:9671272-Pyruvate Dehydrogenase Complex Deficiency Disease,
pubmed-meshheading:9671272-Sequence Analysis, DNA,
pubmed-meshheading:9671272-Transfection
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pubmed:year |
1998
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pubmed:articleTitle |
Arginine 302 mutations in the pyruvate dehydrogenase E1alpha subunit gene: identification of further patients and in vitro demonstration of pathogenicity.
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pubmed:affiliation |
Department of Biochemistry, University of Oxford, United Kingdom.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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