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Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese

PURPOSE: Age-related cataract (ARC) is a complex multi-factorial disorder involving several genetic and environmental factors. The major intrinsic protein of lens fiber gene (MIP) encodes the most abundant junctional membrane protein in the mature lens and plays a critical role in maintainace of len...

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Autores principales: Zhou, Zhou, Wang, Binbin, Luo, Yongfeng, Zhou, Guangkai, Hu, Shanshan, Zhang, Han, Ma, Xu, Qi, Yanhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171496/
https://www.ncbi.nlm.nih.gov/pubmed/21921980
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author Zhou, Zhou
Wang, Binbin
Luo, Yongfeng
Zhou, Guangkai
Hu, Shanshan
Zhang, Han
Ma, Xu
Qi, Yanhua
author_facet Zhou, Zhou
Wang, Binbin
Luo, Yongfeng
Zhou, Guangkai
Hu, Shanshan
Zhang, Han
Ma, Xu
Qi, Yanhua
author_sort Zhou, Zhou
collection PubMed
description PURPOSE: Age-related cataract (ARC) is a complex multi-factorial disorder involving several genetic and environmental factors. The major intrinsic protein of lens fiber gene (MIP) encodes the most abundant junctional membrane protein in the mature lens and plays a critical role in maintainace of lens normal structure and internal circulation. To determine the relationship between single nucleotide polymorphisms (SNPs) in MIP and the susceptibility to ARC in a Chinese population, we conducted this case-control study. METHODS: A total of 164 unrelated ARC patients and 132 normal controls were involved in the study. All participants completed full physical and ophthalmic examinations and provided a blood sample for DNA extraction. Seven SNPs (rs2269348, rs61759527, c.-4T>C, rs77163805, rs74641138, rs35033450, and rs36032520) in MIP were amplified by polymerase chain reaction (PCR) and then sequenced. Statistical analysis was performed using SNPstats. RESULTS: Polymorphisms rs61759527, rs77163805, rs35033450, and rs36032520 were not detected in all 296 subjects. There were no statistical differences in genotype or allele frequency of rs2269348 and rs74641138 between ARC cases and controls. But in c.-4C>T, cataract patients had a higher TC genotype and C allele frequencies (p=0.0018 and p=0.017, respectively) compared to healthy controls. The haplotype CCG of rs2269348, c.-4T>C and rs74641138 also exhibited a significantly higher distribution in cases than controls (OR=8.83, p=0.0024). CONCLUSIONS: Our findings indicate that the genotype TC in polymorphism c.-4T>C and haplotype CCG of rs2269348, c.-4T>C, and rs74641138 in MIP may attach an additional genetic risk factor for ARC in Chinese. This is the first association study about SNPs in MIP and susceptibility to ARC in Chinese population.
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spelling pubmed-31714962011-09-15 Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese Zhou, Zhou Wang, Binbin Luo, Yongfeng Zhou, Guangkai Hu, Shanshan Zhang, Han Ma, Xu Qi, Yanhua Mol Vis Research Article PURPOSE: Age-related cataract (ARC) is a complex multi-factorial disorder involving several genetic and environmental factors. The major intrinsic protein of lens fiber gene (MIP) encodes the most abundant junctional membrane protein in the mature lens and plays a critical role in maintainace of lens normal structure and internal circulation. To determine the relationship between single nucleotide polymorphisms (SNPs) in MIP and the susceptibility to ARC in a Chinese population, we conducted this case-control study. METHODS: A total of 164 unrelated ARC patients and 132 normal controls were involved in the study. All participants completed full physical and ophthalmic examinations and provided a blood sample for DNA extraction. Seven SNPs (rs2269348, rs61759527, c.-4T>C, rs77163805, rs74641138, rs35033450, and rs36032520) in MIP were amplified by polymerase chain reaction (PCR) and then sequenced. Statistical analysis was performed using SNPstats. RESULTS: Polymorphisms rs61759527, rs77163805, rs35033450, and rs36032520 were not detected in all 296 subjects. There were no statistical differences in genotype or allele frequency of rs2269348 and rs74641138 between ARC cases and controls. But in c.-4C>T, cataract patients had a higher TC genotype and C allele frequencies (p=0.0018 and p=0.017, respectively) compared to healthy controls. The haplotype CCG of rs2269348, c.-4T>C and rs74641138 also exhibited a significantly higher distribution in cases than controls (OR=8.83, p=0.0024). CONCLUSIONS: Our findings indicate that the genotype TC in polymorphism c.-4T>C and haplotype CCG of rs2269348, c.-4T>C, and rs74641138 in MIP may attach an additional genetic risk factor for ARC in Chinese. This is the first association study about SNPs in MIP and susceptibility to ARC in Chinese population. Molecular Vision 2011-08-25 /pmc/articles/PMC3171496/ /pubmed/21921980 Text en Copyright © 2011 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhou, Zhou
Wang, Binbin
Luo, Yongfeng
Zhou, Guangkai
Hu, Shanshan
Zhang, Han
Ma, Xu
Qi, Yanhua
Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese
title Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese
title_full Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese
title_fullStr Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese
title_full_unstemmed Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese
title_short Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese
title_sort major intrinsic protein (mip) polymorphism is associated with age-related cataract in chinese
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171496/
https://www.ncbi.nlm.nih.gov/pubmed/21921980
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