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http://purl.uniprot.org/citations/20454697http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20454697http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20454697http://www.w3.org/2000/01/rdf-schema#comment"

Purpose

To screen mitochondrial DNA (mtDNA) variations in Leber hereditary optic neuropathy (LHON).

Methods

Ten LHON patients were selected from neuro-ophthalmology clinics of All India Institute of Medical Sciences (AIIMS), New Delhi, India. Clinical evaluation included slit-lamp biomicroscopy, fundus examination, and neuroimaging. DNA was isolated from whole blood samples. The entire coding region of the mitochondrial genome was amplified by PCR in ten patients and 20 controls. The full mtDNA genome except D-loop was sequenced. All sequences were analyzed against mitochondrial reference sequence NC_012920.

Results

MtDNA sequencing revealed a total of 30 nucleotide variations in the ten LHON patients and 29 in the 20 controls. Of 30 changes, 30.00% (9/30) were nonsynonymous, and the remaining 70.00% (21/30) were synonymous. In controls, a total of five changes were nonsynonymous. Out of the total 14 nonsynonymous changes observed in cases and controls, four (p.A52T in nicotinamide adenine dinucleotide [NADH] dehydrogenase [ND1] protein; p.L128Q in ND2; p.W48R in ATPase6; p.R340H in ND4 protein) were pathogenic. Four patients were positive for either of pathogenic changes. In total, 16.66% (5/30) variations were novel out of which 40.00% (2/5) were nonsynonymous. All novel variations were submitted to the GenBank database, and accession numbers were obtained. Primary LHON mutations in complex I genes have been considered a hallmark feature of LHON patients, and primary LHON mutations were present in two cases in this study. Mutations in complex I genes (ND genes) account for 50%-90% of LHON pedigrees in different ethnic pedigrees. In this study the highest numbers of changes were also present in complex I genes (46.66%; 14/30) followed by complex IV (30.00%; 9/30), complex III (16.66%; 5/30), and then complex V (6.66%; 2/30). Complex I had 5/30 (16.66%) nonsynonymous changes, complex III had 1/30 (3.33%), complex IV had 1/30 (3.33%), and complex V had 2/30 (6.66%) nonsynonymous changes. Nonsynonymous mutations in cytochrome c oxidase (COX) genes have been reported previously in LHON patients. Nonsynonymous mtDNA variations may adversely affect the respiratory chain and impair the oxidative phosphorylation (OXPHOS) pathway, resulting in low ATP production and elevated reactive oxygen species (ROS) levels, which cause oxidative stress. It has previously been reported that oxidative stress (OS) leads to oxidative damage of cellular macromolecules, such as mitochondrial and nuclear DNA, proteins, and lipids along with energy depletion and a local imbalance of calcium homeostasis, resulting in neuronal degeneration. OS is the underlying etiology in several ocular diseases and also plays an essential role in LHON.

Conclusions

A total of five novel mtDNA variations were identified in this study. Nonsynonymous mtDNA variations may adversely affect the respiratory chain and impair the OXPHOS pathway, resulting in low ATP production and elevated ROS levels. OS further damages both nuclear and mtDNA. This preliminary study describes mtDNA sequence variations in a relatively small number of LHON patients of north Indian ethnic origin. However, these results should be confirmed in other populations. Early diagnosis of mtDNA variations and prompt anti-oxidant administration in these cases may delay OS-induced injury to retinal ganglion cells (RGCs) and hence improve visual prognosis."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Sharma P."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Sharma P."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Kumar M."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Kumar M."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Saxena R."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Saxena R."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Dada R."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Dada R."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Tanwar M."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/author"Tanwar M."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/name"Mol. Vis."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/name"Mol Vis"xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/pages"782-792"xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/pages"782-792"xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/title"Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/title"Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy."xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/volume"16"xsd:string
http://purl.uniprot.org/citations/20454697http://purl.uniprot.org/core/volume"16"xsd:string
http://purl.uniprot.org/citations/20454697http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/20454697
http://purl.uniprot.org/citations/20454697http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/20454697
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