Identification and genotype phenotype correlation of novel mutations in SIX6 gene in primary open angle glaucoma. (4th May 2018)

• Record Type: Journal Article
• Authors: Mohanty, Kuldeep; Dada, Rima; Dada, Tanuj
• Is Part Of: Ophthalmic genetics. Volume 39:Number 3(2018)
• Page Start: 366
• Page End: 372
• Publication Date: 2018-05-04
• Subjects: Glaucoma -- SIX1 -- SIX6 -- visual field; Eye -- Diseases -- Genetic aspects -- Periodicals; Eye Diseases -- genetics -- Periodicals; Eye Diseases -- in infancy & childhood -- Periodicals; 617.7
• DOI: 10.1080/13816810.2018.1432062
• Languages: English
• ISSNs: 1381-6810

Abstract

ABSTRACT: Background: Recently SIX1 and SIX6 genes have been associated with primary open angle glaucoma (POAG). This study was planned to do mutation screening in SIX1 and SIX6 genes in North Indian POAG patients and correlate with clinical phenotypes. Materials and Methods: SIX1 and SIX6 genes were amplified by PCR and sequenced in 115 POAG cases and 105 controls. Four pathogenecity prediction tools (MutationTaster, PolyPhen-2 HumDiv, PolyPhen-2 HumVar and SIFT) were used to predict the pathogenicity of the missense mutations. Protein modeling studies were done to predict the effect of the missense mutations on the protein structure and function. Results: Two novel mutations p.R116G and p.R116E were observed in the SIX6 gene of patients with POAG. The mutations p.R116G and p.R116E were predicted to be pathogenic and replacement of R116 by G or E might lead to loss of interaction between DNA and R116 of wild type SIX6 protein. The patients with the mutation p.R116E had significantly more visual field damage (MD) and early age of onset of the disease. No sequence variations were observed in the SIX1 gene. Conclusion: These results expand the mutation spectrum of SIX6 gene and suggest that SIX6 gene plays an important role in POAG pathogenesis.