Common variants within MECP2 confer risk of systemic lupus erythematosus

Citations of this article
Mendeley users who have this article in their library.


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 regulation of methylation-sensitive genes. Utilizing a candidate gene association, we genotyped 21 SNPs within and around MECP2 in SLE patiehts 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.




Sawalha, A. H., Webb, R., Han, S., Kelly, J. A., Kaufman, K. M., Kimberly, R. P., … Harley, J. B. (2008). Common variants within MECP2 confer risk of systemic lupus erythematosus. PLoS ONE, 3(3).

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free