Mutational analysis of TYR gene and its structural consequences in OCA1A.

Abstract

Oculocutaneous albinism type 1A (OCA1A) is the most severe form of albinism characterized by a complete lack of melanin production throughout life and is caused by mutations in the TYR gene. TYR gene codes tyrosinase protein to its relation with melanin formation by knowing the function of these SNPs. Based on the computational approaches, we have analyzed the genetic variations that could change the functional behaviour by altering the structural arrangement in TYR protein which is responsible for OCA1A. Consequences of mutation on TYR structure were observed by analyzing the flexibility behaviour of native and mutant tyrosinase protein. Mutations T373K, N371Y, M370T and P313R were suggested as high deleterious effect on TYR protein and it is responsible for OCA1A which were also endorsed with previous in vivo experimental studies. Based on the quantitative assessment and flexibility analysis of OCA1A variants, T373K showed the most deleterious effect. Our analysis determines that certain mutations can affect the dynamic properties of protein and can lead to disease conditions. This study provides a significant insight into the underlying molecular mechanism involved in albinism associated with OCA1A.

• Authors: Balu K, Rituraj Purohit
• Journal: Gene (Gene) Vol. 513 Issue 1 Pg. 184-95 (Jan 15 2013) ISSN: 1879-0038 [Electronic] Netherlands
• PMID: 23085273 (Publication Type: Journal Article)
• Copyright: Copyright © 2012 Elsevier B.V. All rights reserved.

Chemical References

• Melanins
• Monophenol Monooxygenase

Topics

• Albinism, Oculocutaneous (genetics)
• DNA Mutational Analysis
• Data Mining
• Gene Frequency
• Genetic Variation
• Humans
• Melanins (biosynthesis, genetics)
• Monophenol Monooxygenase (chemistry, genetics)
• Polymorphism, Single Nucleotide
• Protein Conformation
• Severity of Illness Index