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在中国汉族圆锥角膜患者的 ECM 相关基因中发现了三个新的变体。

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

机构信息

Department of Ophthalmology, The Second Affiliated Hospital of Zhejiang University, College of Medicine, Hangzhou, Zhejiang, China.

出版信息

Sci Rep. 2020 Apr 3;10(1):5844. doi: 10.1038/s41598-020-62572-0.

Abstract

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.

摘要

作为角膜移植的主要指征,圆锥角膜的发病机制仍不清楚。本研究旨在探讨细胞外基质(ECM)相关基因突变是否与中国汉族散发型圆锥角膜(KC)患者有关。共纳入 153 名参与者,包括 53 名 KC 患者和 100 名健康对照者。采用下一代测序和 Sanger 测序对 3 个 ECM 相关基因(LOX、COL5A1 和 TIMP3)进行突变分析。为了进一步证实 3 个 ECM 相关基因在圆锥角膜发病机制中的作用,我们进行了体外实时定量 PCR。结果显示,在 KC 患者的上述 ECM 相关基因中发现了 3 个新的序列变异(LOX 中的 c.95G>A、COL5A1 中的 c.1372C>T 和 TIMP3 中的 c.476C>T),而在健康对照组中未检测到。根据 QPCR 结果,我们发现 LOX 和 TIMP3 的表达水平在 KC 患者中降低,而 COL5A1 的表达无显著差异。这是首次在中国人圆锥角膜患者中使用下一代测序筛选如此多的 ECM 相关基因。我们发现了许多潜在的致病变异,扩大了许多突变谱,为其他研究人员提供了进一步研究和验证的新位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/492c/7125089/8f41406b82aa/41598_2020_62572_Fig1_HTML.jpg

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