Suppr超能文献

eQTL数据中的基因集富集鉴定出新型注释和通路调控因子。

Gene set enrichment in eQTL data identifies novel annotations and pathway regulators.

作者信息

Wu Chunlei, Delano David L, Mitro Nico, Su Stephen V, Janes Jeff, McClurg Phillip, Batalov Serge, Welch Genevieve L, Zhang Jie, Orth Anthony P, Walker John R, Glynne Richard J, Cooke Michael P, Takahashi Joseph S, Shimomura Kazuhiro, Kohsaka Akira, Bass Joseph, Saez Enrique, Wiltshire Tim, Su Andrew I

机构信息

Genomics Institute of the Novartis Research Foundation, San Diego, California, United States of America.

出版信息

PLoS Genet. 2008 May 9;4(5):e1000070. doi: 10.1371/journal.pgen.1000070.

Abstract

Genome-wide gene expression profiling has been extensively used to generate biological hypotheses based on differential expression. Recently, many studies have used microarrays to measure gene expression levels across genetic mapping populations. These gene expression phenotypes have been used for genome-wide association analyses, an analysis referred to as expression QTL (eQTL) mapping. Here, eQTL analysis was performed in adipose tissue from 28 inbred strains of mice. We focused our analysis on "trans-eQTL bands", defined as instances in which the expression patterns of many genes were all associated to a common genetic locus. Genes comprising trans-eQTL bands were screened for enrichments in functional gene sets representing known biological pathways, and genes located at associated trans-eQTL band loci were considered candidate transcriptional modulators. We demonstrate that these patterns were enriched for previously characterized relationships between known upstream transcriptional regulators and their downstream target genes. Moreover, we used this strategy to identify both novel regulators and novel members of known pathways. Finally, based on a putative regulatory relationship identified in our analysis, we identified and validated a previously uncharacterized role for cyclin H in the regulation of oxidative phosphorylation. We believe that the specific molecular hypotheses generated in this study will reveal many additional pathway members and regulators, and that the analysis approaches described herein will be broadly applicable to other eQTL data sets.

摘要

全基因组基因表达谱分析已被广泛用于基于差异表达生成生物学假设。最近,许多研究使用微阵列来测量遗传作图群体中的基因表达水平。这些基因表达表型已用于全基因组关联分析,这种分析被称为表达数量性状基因座(eQTL)定位。在此,我们对来自28个近交系小鼠的脂肪组织进行了eQTL分析。我们将分析重点放在“反式eQTL带”上,其定义为许多基因的表达模式都与一个共同遗传位点相关的情况。我们筛选了构成反式eQTL带的基因,以确定其在代表已知生物学途径的功能基因集中的富集情况,并将位于相关反式eQTL带位点的基因视为候选转录调节因子。我们证明,这些模式在已知上游转录调节因子与其下游靶基因之间的先前表征关系中得到了富集。此外,我们使用这种策略来鉴定已知途径的新调节因子和新成员。最后,基于我们分析中确定的假定调节关系,我们鉴定并验证了细胞周期蛋白H在氧化磷酸化调节中一个先前未被表征的作用。我们相信,本研究中产生的特定分子假设将揭示许多其他途径成员和调节因子,并且本文所述的分析方法将广泛适用于其他eQTL数据集。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验