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MECP2基因内的常见变异会增加患系统性红斑狼疮的风险。

Common variants within MECP2 confer risk of systemic lupus erythematosus.

作者信息

Sawalha Amr H, Webb Ryan, Han Shizhong, Kelly Jennifer A, Kaufman Kenneth M, Kimberly Robert P, Alarcón-Riquelme Marta E, James Judith A, Vyse Timothy J, Gilkeson Gary S, Choi Chan-Bum, Scofield R Hal, Bae Sang-Cheol, Nath Swapan K, Harley John B

机构信息

Department of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.

出版信息

PLoS One. 2008 Mar 5;3(3):e1727. doi: 10.1371/journal.pone.0001727.

Abstract

Systemic lupus erythematosus (SLE) is a predominantly female autoimmune disease that affects multiple organ systems. Herein, we report on an X-chromosome gene association with SLE. Methyl-CpG-binding protein 2 (MECP2) is located on chromosome Xq28 and encodes for a protein that plays a critical role in epigenetic transcriptional regulation of methylation-sensitive genes. Utilizing a candidate gene association approach, we genotyped 21 SNPs within and around MECP2 in SLE patients and controls. We identify and replicate association between SLE and the genomic element containing MECP2 in two independent SLE cohorts from two ethnically divergent populations. These findings are potentially related to the overexpression of methylation-sensitive genes in SLE.

摘要

系统性红斑狼疮(SLE)是一种主要影响女性的自身免疫性疾病,可累及多个器官系统。在此,我们报告了一个与SLE相关的X染色体基因。甲基化CpG结合蛋白2(MECP2)位于Xq28染色体上,编码一种在甲基化敏感基因的表观遗传转录调控中起关键作用的蛋白质。利用候选基因关联方法,我们对SLE患者和对照组中MECP2基因内部及周围的21个单核苷酸多态性(SNP)进行了基因分型。我们在来自两个种族不同人群的两个独立SLE队列中,鉴定并重复了SLE与包含MECP2的基因组元件之间的关联。这些发现可能与SLE中甲基化敏感基因的过表达有关。

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