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Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients

As the primary indication for corneal transplantation, the pathogenesis of keratoconus remains elusive. Aiming to identify whether any mutation from extracellular-matrix (ECM)-related genes contributes to the patients with sporadic cases of keratoconus (KC) from Chinese Han population, one hundred a...

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Autores principales: Xu, Xiayan, Zhang, Xin, Cui, Yilei, Yang, Hao, Ping, Xiyuan, Wu, Jing, Yu, Xiaoning, Jin, Xiuming, Huang, Xiaodan, Shentu, Xingchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125089/
https://www.ncbi.nlm.nih.gov/pubmed/32246022
http://dx.doi.org/10.1038/s41598-020-62572-0
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author Xu, Xiayan
Zhang, Xin
Cui, Yilei
Yang, Hao
Ping, Xiyuan
Wu, Jing
Yu, Xiaoning
Jin, Xiuming
Huang, Xiaodan
Shentu, Xingchao
author_facet Xu, Xiayan
Zhang, Xin
Cui, Yilei
Yang, Hao
Ping, Xiyuan
Wu, Jing
Yu, Xiaoning
Jin, Xiuming
Huang, Xiaodan
Shentu, Xingchao
author_sort Xu, Xiayan
collection PubMed
description As the primary indication for corneal transplantation, the pathogenesis of keratoconus remains elusive. Aiming to identify whether any mutation from extracellular-matrix (ECM)-related genes contributes to the patients with sporadic cases of keratoconus (KC) from Chinese Han population, one hundred and fifty-three participants in total were enrolled in our study, including fifty-three KC patients and one hundred healthy controls. Mutational analysis of three ECM-related genes (LOX, COL5A1 and TIMP3) with next-generation sequencing and Sanger sequencing was performed. To further confirm the function of three ECM-related genes in the pathogenesis of keratoconus, we performed Real-time Quantitative PCR in vitro. Results showed that three new sequence variants (c.95 G > A in LOX, c.1372 C > T in COL5A1 and c.476 C > T in TIMP3) were identified in aforementioned ECM-related genes in KC patients without being detected among the healthy controls. According to the results of QPCR, we found that the expression levels of LOX and TIMP3 were decreased in the KC patients, while COL5A1 showed no significant difference of expression. This is the first time to screen so many ECM-related genes in Chinese keratoconus patients using next-generation sequencing. We find numerous underlying causal variants, enlarging lots of mutation spectrums and thus providing new sites for other investigators to replicate and for further research.
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spelling pubmed-71250892020-04-08 Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients Xu, Xiayan Zhang, Xin Cui, Yilei Yang, Hao Ping, Xiyuan Wu, Jing Yu, Xiaoning Jin, Xiuming Huang, Xiaodan Shentu, Xingchao Sci Rep Article As the primary indication for corneal transplantation, the pathogenesis of keratoconus remains elusive. Aiming to identify whether any mutation from extracellular-matrix (ECM)-related genes contributes to the patients with sporadic cases of keratoconus (KC) from Chinese Han population, one hundred and fifty-three participants in total were enrolled in our study, including fifty-three KC patients and one hundred healthy controls. Mutational analysis of three ECM-related genes (LOX, COL5A1 and TIMP3) with next-generation sequencing and Sanger sequencing was performed. To further confirm the function of three ECM-related genes in the pathogenesis of keratoconus, we performed Real-time Quantitative PCR in vitro. Results showed that three new sequence variants (c.95 G > A in LOX, c.1372 C > T in COL5A1 and c.476 C > T in TIMP3) were identified in aforementioned ECM-related genes in KC patients without being detected among the healthy controls. According to the results of QPCR, we found that the expression levels of LOX and TIMP3 were decreased in the KC patients, while COL5A1 showed no significant difference of expression. This is the first time to screen so many ECM-related genes in Chinese keratoconus patients using next-generation sequencing. We find numerous underlying causal variants, enlarging lots of mutation spectrums and thus providing new sites for other investigators to replicate and for further research. Nature Publishing Group UK 2020-04-03 /pmc/articles/PMC7125089/ /pubmed/32246022 http://dx.doi.org/10.1038/s41598-020-62572-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xu, Xiayan
Zhang, Xin
Cui, Yilei
Yang, Hao
Ping, Xiyuan
Wu, Jing
Yu, Xiaoning
Jin, Xiuming
Huang, Xiaodan
Shentu, Xingchao
Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients
title Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients
title_full Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients
title_fullStr Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients
title_full_unstemmed Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients
title_short Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients
title_sort three novel variants identified within ecm-related genes in chinese han keratoconus patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125089/
https://www.ncbi.nlm.nih.gov/pubmed/32246022
http://dx.doi.org/10.1038/s41598-020-62572-0
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