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Neuromuscul Disord. 1995 Sep;5(5):391-8.

A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene.

Author information

1
H. Houston Merritt Clinical Research Center for Muscular Dystrophy and Related Disorders, New York, USA.

Abstract

We report a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) who harbored a novel missense mutation at mtDNA position 9957 in the gene specifying subunit III of cytochrome c oxidase (COX III). This T-->C transition converted Phe-251, a highly conserved amino acid in the C-terminus of the polypeptide, to Leu. The mutation, which was not present in 107 normal controls or in 57 patients with various mitochondrial diseases, was heteroplasmic in both muscle and blood of the proband and in blood from his asymptomatic mother. These results provide evidence that the MELAS clinical phenotype can be due not only to mutations in mtDNA-encoded tRNA genes, but in polypeptide-coding genes as well.

PMID:
7496173
[Indexed for MEDLINE]

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