Nischan Jennifer, Gatalica Zoran, Curtis Mindee, Lenk Guy M, Tromp Gerard, Kuivaniemi Helena
Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, Michigan,USA.
Circ Cardiovasc Genet. 2009 Dec;2(6):565-72. doi: 10.1161/CIRCGENETICS.108.843854. Epub 2009 Oct 19.
Previously, we identified 3274 distinct differentially expressed genes in abdominal aortic aneurysm (AAA) tissue compared with nonaneurysmal controls. As transcriptional control is responsible for these expression changes, we sought to find common transcriptional elements in the promoter regions of the differentially expressed genes.
We analyzed the up- and downregulated gene sets with Whole Genome rVISTA to determine the transcription factor (TF) binding sites overrepresented in the 5-kb promoter regions of the 3274 genes. The downregulated gene set yielded 144 TF binding sites that were overrepresented in the subset when compared with the entire genome. In contrast, the upregulated gene set yielded only 13 distinct overrepresented TF binding sites. Interestingly, as classified by TRANSFAC, 8 of the 13 TFs binding to these regions belong to the ETS family. Additionally, nuclear factor kB and its subunits p50 and p65 showed enrichment. Immunohistochemical analyses of 10 TFs from the upregulated set showed 9 to be present in AAA tissue. Based on gene ontology analysis of biological process categories of the upregulated target genes of enriched TFs, 10 TFs had enrichment in immune system process among their target genes.
Our genome-wide analysis provides further evidence of ETS and nuclear factor kB involvement in AAA. Additionally, our results provide novel insight for future studies aiming to dissect the pathogenesis of AAA and have uncovered potential therapeutic targets for AAA prevention.
此前,我们鉴定出与非动脉瘤对照相比,腹主动脉瘤(AAA)组织中有3274个不同的差异表达基因。由于转录调控导致了这些表达变化,我们试图在差异表达基因的启动子区域寻找共同的转录元件。
我们使用全基因组rVISTA分析上调和下调的基因集,以确定在3274个基因的5kb启动子区域中过度表达的转录因子(TF)结合位点。与整个基因组相比,下调的基因集产生了144个在子集中过度表达的TF结合位点。相比之下,上调的基因集仅产生了13个不同的过度表达的TF结合位点。有趣的是,根据TRANSFAC分类,与这些区域结合的13个TF中有8个属于ETS家族。此外,核因子kB及其亚基p50和p65也显示出富集。对上调组中的10个TF进行免疫组织化学分析,结果显示9个在AAA组织中存在。基于对富集TF的上调靶基因的生物学过程类别的基因本体分析,10个TF在其靶基因中的免疫系统过程中存在富集。
我们的全基因组分析为ETS和核因子kB参与AAA提供了进一步的证据。此外,我们的结果为未来旨在剖析AAA发病机制的研究提供了新的见解,并发现了预防AAA的潜在治疗靶点。