4.6 Article

Common Variants within MECP2 Confer Risk of Systemic Lupus Erythematosus

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PLOS ONE
卷 3, 期 3, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0001727

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资金

  1. NIH [P20-RR015577, AI63622, AR42460, AI024717, AI31584, AR62277, AR048940, AR0490084]
  2. University of Oklahoma College of Medicine (AHS)
  3. Kirkland Scholar award
  4. Alliance for Lupus Research
  5. U.S. Department of Veterans Affairs
  6. National Research Foundation of Korea [전06A1116] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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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