1. Novel mitochondrial mutation in the ND4 gene associated with Leigh syndrome
- Author
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G. P. Rajshekher, Alla G. Reddy, Manjunath B. Joshi, Lalji Singh, Kumarasamy Thangaraj, and Ayyasamy Vanniarajan
- Subjects
Mitochondrial DNA ,Nuclear gene ,DNA Mutational Analysis ,Molecular Sequence Data ,Mutation, Missense ,Mitochondrion ,Biology ,DNA, Mitochondrial ,Basal Ganglia ,Basal Ganglia Diseases ,medicine ,Humans ,Missense mutation ,Genetic Predisposition to Disease ,Histidine ,Amino Acid Sequence ,Leigh disease ,Gene ,Genetics ,Homoplasmy ,Electron Transport Complex I ,Infant ,General Medicine ,medicine.disease ,Magnetic Resonance Imaging ,Protein Subunits ,Amino Acid Substitution ,Neurology ,Mutation (genetic algorithm) ,Tyrosine ,Female ,Neurology (clinical) ,Leigh Disease - Abstract
We analyzed the complete mitochondrial genome of a 3-month-old female child with basal ganglionic lesions and other clinical features suggestive of Leigh syndrome, which is caused by variations in mitochondrial and nuclear genes. Our study revealed a novel, homoplasmic T11984C missense mutation in ND4 gene, which replaces a highly conserved amino acid tyrosine with histidine. Computational analysis showed that this mutation alters the secondary structure of ND4 subunit. As the mutation observed in this study was novel and homoplasmic, we speculate that there could be interplay of this mitochondrial mutation along with nuclear gene(s) in the pathogenesis.
- Published
- 2006
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