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Genetic architecture of transcript-level variation in humans
被引:103
|作者:
Duan, Shiwei
[1
]
Huang, R. Stephanie
[1
]
Zhang, Wei
[1
]
Bleibel, Wasim K.
[1
]
Roe, Cheryl A.
[2
]
Clark, Tyson A.
[3
]
Chen, Tina X.
[3
]
Schweitzer, Anthony C.
[3
]
Blume, John E.
[3
]
Cox, Nancy J.
[2
]
Dolan, M. Eileen
[1
]
机构:
[1] Univ Chicago, Dept Med, Hematol Oncol Sect, Chicago, IL 60637 USA
[2] Univ Chicago, Med Genet Sect, Dept Med & Human Genet, Chicago, IL 60637 USA
[3] Affymetrix Inc, Affymetrix Lab, Express Res, Santa Clara, CA 95051 USA
关键词:
D O I:
10.1016/j.ajhg.2008.03.006
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
We report here the results of testing the pairwise association of 12,747 transcriptional gene-expression values with more than two million single-nucleotide polymorphisms (SNPs) in samples of European (CEPH from Utah; CEU) and African (Yoruba from Ibadan; YRI) ancestry. We found 4,677 and 5,125 significant associations between expression quantitative nucleotides (eQTNs) and transcript clusters in the CEU and the YRI samples, respectively. The physical distance between an eQTN and its associated transcript cluster was referred to as the intrapair distance. An association with 4 Mb or less intrapair distance was defined as local; otherwise, it was defined as distant. The enrichment analysis of functional categories shows that genes harboring the local eQTNs are enriched in the categories related to nucleosome and chromatin assembly; the genes harboring the distant eQTNs are enriched in the categories related to transmembrane signal transduction, suggesting that these biological pathways are likely to play a significant role in regulation of gene expression. We highlight in the EPHX1 gene a deleterious nonsynonymous SNP that is distantly associated with gene expression of ORMDL3, a susceptibility gene for asthma.
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页码:1101 / 1113
页数:13
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