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Common Variants within MECP2 Confer Risk of Systemic Lupus Erythematosusopen access

Authors
Sawalha, Amr H.Webb, RyanHan, ShizhongKelly, Jennifer A.Kaufman, Kenneth M.Kimberly, Robert P.Alarcon-Riquelme, Marta E.James, Judith A.Vyse, Timothy J.Gilkeson, Gary S.Choi, Chan-BumScofield, R. HalBae, Sang-CheolNath, Swapan K.Harley, John B.
Issue Date
Mar-2008
Publisher
PUBLIC LIBRARY SCIENCE
Citation
PLOS ONE, v.3, no.3, pp.1 - 7
Indexed
SCIE
SCOPUS
Journal Title
PLOS ONE
Volume
3
Number
3
Start Page
1
End Page
7
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/178914
DOI
10.1371/journal.pone.0001727
ISSN
1932-6203
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.
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