4.3 Article

Detecting Genetic Associations between ATG5 and Lupus Nephritis by trans-eQTL

期刊

JOURNAL OF IMMUNOLOGY RESEARCH
卷 2015, 期 -, 页码 -

出版社

HINDAWI LTD
DOI: 10.1155/2015/153132

关键词

-

资金

  1. National Natural Science Foundation of China [81200524]
  2. Foundation of Ministry of Education of China [20120001120008]
  3. Beijing Natural Science Foundation [7152148]
  4. Major State Basic Research Development Program of China (973 program) [2012CB517700]
  5. Research Fund of Beijing Municipal Science and Technology for the Outstanding Ph.D. Program [20121000110]
  6. Natural Science Fund of China to the Innovation Research Group [81021004]

向作者/读者索取更多资源

Objectives. Numerous loci were identified to perturb gene expression in trans. As elevated ATG5 expression was observed in systemic lupus erythematosus (SLE), the study was conducted to analyze the genome-wide genetic regulatory mechanisms associated with ATG5 expression in a Chinese population with lupus nephritis (LN). Methods. The online expression quantitative trait loci database was searched for trans-expression single nucleotide polymorphisms (trans-eSNPs) of ATG5. Tagging trans-eSNPs were genotyped by a custom-made genotyping chip in 280 patients and 199 controls. For positive findings, clinical information and bioinformation analyses were performed. Results. Four trans-eSNPs were observed to be associated with susceptibility to LN (P < 0.05), including ANKRD50 rs17008504, AGA rs2271100, PAK7 rs6056923, and TET2 rs1391441, while seven other trans-eSNPs showed marginal significant associations (0.05 < P < 0.1). Correlations between the trans-eSNPs and ATG5 expression and different expression levels of ATG5 in SLE patients and controls were validated, and their regulatory effects were annotated. However, no significant associations were observed between different genotypes of trans-eSNPs and severity or outcome of the patients. Conclusion. Using the new systemic genetics approach, we identified 10 loci associated with susceptibility to LN potentially, which may be complementary to future pathway based genetic studies.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据