Novel Mutations in COL6A3 That Associated With Peters’ Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative Stress

Peters’ anomaly (PA) is a rare form of anterior segment dysgenesis characterized by central corneal opacity accompanied by iridocorneal or lenticulo-corneal adhesions. Although genetic mutations, particularly those affecting transcription factors that function in eye development, are known to cause...

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Main Authors: Yue Li, Jing Zhang, Yiqin Dai, Yidan Fan, Jianjiang Xu
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2020.531986/full
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spelling doaj-b1be38d220de4af2876ed9830d238a452020-11-25T04:05:25ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2020-11-01810.3389/fcell.2020.531986531986Novel Mutations in COL6A3 That Associated With Peters’ Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative StressYue Li0Yue Li1Yue Li2Jing Zhang3Jing Zhang4Jing Zhang5Yiqin Dai6Yiqin Dai7Yiqin Dai8Yidan Fan9Yidan Fan10Yidan Fan11Jianjiang Xu12Jianjiang Xu13Jianjiang Xu14Eye Institute and Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai, ChinaNHC Key Laboratory of Myopia, Fudan University, Shanghai, ChinaShanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, ChinaEye Institute and Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai, ChinaNHC Key Laboratory of Myopia, Fudan University, Shanghai, ChinaShanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, ChinaEye Institute and Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai, ChinaNHC Key Laboratory of Myopia, Fudan University, Shanghai, ChinaShanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, ChinaEye Institute and Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai, ChinaNHC Key Laboratory of Myopia, Fudan University, Shanghai, ChinaShanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, ChinaEye Institute and Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai, ChinaNHC Key Laboratory of Myopia, Fudan University, Shanghai, ChinaShanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, ChinaPeters’ anomaly (PA) is a rare form of anterior segment dysgenesis characterized by central corneal opacity accompanied by iridocorneal or lenticulo-corneal adhesions. Although genetic mutations, particularly those affecting transcription factors that function in eye development, are known to cause PA, the etiology of this disease remains poorly understood. In this study, 23 patients with PA were recruited for panel sequencing. Four out of 23 patients were found to carry variants in known PA causal genes, PITX2 and PITX3. More importantly, two homozygous mutations (NM_057164: p.Val86Ala and p.Arg689Cys) in the COL6A3 gene (collagen type VI alpha-3 chain) that correlated with the phenotype of type I PA were identified, and then validated by following whole-exome sequencing. The expression profile of the COL6A3 gene in the cornea and the impact of the mutations on protein physiological processing and cellular function were further explored. It was shown that COL6A3 presented relatively high expression in the cornea. The mutant COL6A3 protein was relatively retained intracellularly, and its expression reduced cellular resistance to oxidative stress through an enhanced endoplasmic reticulum stress response. Taken together, our findings expanded the known genetic spectrum of PA, and provided evidence for the involvement of COL6A3 or collagen VI in ocular anterior segment development, thereby offering new insight for future investigations targeting PA.https://www.frontiersin.org/articles/10.3389/fcell.2020.531986/fullPeters’ anomalyanterior segment dysgenesisCOL6A3endoplasmic reticulum stressoxidative stressapoptosis
collection DOAJ
language English
format Article
sources DOAJ
author Yue Li
Yue Li
Yue Li
Jing Zhang
Jing Zhang
Jing Zhang
Yiqin Dai
Yiqin Dai
Yiqin Dai
Yidan Fan
Yidan Fan
Yidan Fan
Jianjiang Xu
Jianjiang Xu
Jianjiang Xu
spellingShingle Yue Li
Yue Li
Yue Li
Jing Zhang
Jing Zhang
Jing Zhang
Yiqin Dai
Yiqin Dai
Yiqin Dai
Yidan Fan
Yidan Fan
Yidan Fan
Jianjiang Xu
Jianjiang Xu
Jianjiang Xu
Novel Mutations in COL6A3 That Associated With Peters’ Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative Stress
Frontiers in Cell and Developmental Biology
Peters’ anomaly
anterior segment dysgenesis
COL6A3
endoplasmic reticulum stress
oxidative stress
apoptosis
author_facet Yue Li
Yue Li
Yue Li
Jing Zhang
Jing Zhang
Jing Zhang
Yiqin Dai
Yiqin Dai
Yiqin Dai
Yidan Fan
Yidan Fan
Yidan Fan
Jianjiang Xu
Jianjiang Xu
Jianjiang Xu
author_sort Yue Li
title Novel Mutations in COL6A3 That Associated With Peters’ Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative Stress
title_short Novel Mutations in COL6A3 That Associated With Peters’ Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative Stress
title_full Novel Mutations in COL6A3 That Associated With Peters’ Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative Stress
title_fullStr Novel Mutations in COL6A3 That Associated With Peters’ Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative Stress
title_full_unstemmed Novel Mutations in COL6A3 That Associated With Peters’ Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative Stress
title_sort novel mutations in col6a3 that associated with peters’ anomaly caused abnormal intracellular protein retention and decreased cellular resistance to oxidative stress
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2020-11-01
description Peters’ anomaly (PA) is a rare form of anterior segment dysgenesis characterized by central corneal opacity accompanied by iridocorneal or lenticulo-corneal adhesions. Although genetic mutations, particularly those affecting transcription factors that function in eye development, are known to cause PA, the etiology of this disease remains poorly understood. In this study, 23 patients with PA were recruited for panel sequencing. Four out of 23 patients were found to carry variants in known PA causal genes, PITX2 and PITX3. More importantly, two homozygous mutations (NM_057164: p.Val86Ala and p.Arg689Cys) in the COL6A3 gene (collagen type VI alpha-3 chain) that correlated with the phenotype of type I PA were identified, and then validated by following whole-exome sequencing. The expression profile of the COL6A3 gene in the cornea and the impact of the mutations on protein physiological processing and cellular function were further explored. It was shown that COL6A3 presented relatively high expression in the cornea. The mutant COL6A3 protein was relatively retained intracellularly, and its expression reduced cellular resistance to oxidative stress through an enhanced endoplasmic reticulum stress response. Taken together, our findings expanded the known genetic spectrum of PA, and provided evidence for the involvement of COL6A3 or collagen VI in ocular anterior segment development, thereby offering new insight for future investigations targeting PA.
topic Peters’ anomaly
anterior segment dysgenesis
COL6A3
endoplasmic reticulum stress
oxidative stress
apoptosis
url https://www.frontiersin.org/articles/10.3389/fcell.2020.531986/full
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