Suppr超能文献

Xylosyltransferase 2 纯合变异导致脊椎-眼综合征。

Homozygous XYLT2 variants as a cause of spondyloocular syndrome.

机构信息

Institute of Human Genetics, Helmholtz Zentrum Munchen, Neuherberg, Germany.

Institute of Human Genetics, Technische Universitat, Munchen, Germany.

出版信息

Clin Genet. 2018 Apr;93(4):913-918. doi: 10.1111/cge.13179. Epub 2018 Feb 20.

Abstract

Spondyloocular syndrome (SOS) is a rare autosomal recessive, skeletal disorder. Two recent studies have shown that it is the result of biallelic sequence variants in the XYLT2 gene with pleiotropic effects in multiple organs, including retina, heart muscle, inner ear, cartilage, and bone. The XYLT2 gene encodes xylosyltransferase 2, which catalyzes the transfer of xylose (monosaccharide) to the core protein of proteoglycans (PGs) leading to initiating the process of PG assembly. SOS was originally characterized in 2 families A and B of Iraqi and Turkish origin, respectively. Using DNA from affected members of the same 2 families, we performed whole exome sequencing, which revealed 2 novel homozygous missense variants (c.1159C > T, p.Arg387Trp) and (c.2548G > C, p.Asp850His). Our findings extend the body of evidence that SOS is caused by homozygous variants in the XYLT2 gene. In addition, this report has extended the phenotypic description of SOS by adding follow-up data from 5 affected individuals in one of the two families, presented here.

摘要

脊柱眼综合征(SOS)是一种罕见的常染色体隐性骨骼疾病。最近的两项研究表明,它是 XYLT2 基因中双等位基因序列变异的结果,在多个器官中具有多效性效应,包括视网膜、心肌、内耳、软骨和骨骼。XYLT2 基因编码木糖基转移酶 2,它催化木糖(单糖)向蛋白聚糖(PGs)核心蛋白的转移,从而启动 PG 组装过程。SOS 最初分别在来自伊拉克和土耳其的 2 个家族 A 和 B 中进行了描述。我们使用来自同一 2 个家族中受影响成员的 DNA 进行了全外显子组测序,发现了 2 个新的纯合错义变异(c.1159C>T,p.Arg387Trp)和(c.2548G>C,p.Asp850His)。我们的发现扩展了证据表明 SOS 是由 XYLT2 基因中的纯合变异引起的。此外,本报告通过添加在此处介绍的两个家族之一的 5 名受影响个体的随访数据,扩展了 SOS 的表型描述。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验