ENCODE芯片测序数据中转录辅因子基序的细胞类型和转录因子特异性富集。

Cell-type and transcription factor specific enrichment of transcriptional cofactor motifs in ENCODE ChIP-seq data.

作者信息

Goi Chin, Little Peter, Xie Chao

出版信息

BMC Genomics. 2013;14 Suppl 5(Suppl 5):S2. doi: 10.1186/1471-2164-14-S5-S2. Epub 2013 Oct 16.

Abstract

BACKGROUND

Cell type and TF specific interactions between Transcription Factors (TFs) and cofactors are essential for transcriptional regulation through recruitment of general transcription machinery to gene promoter regions and their identification heavily reliant on protein interaction assays.

RESULTS

Using TF targeted chromatin immunoprecipitation coupled with massively parallel sequencing (ChIP-seq) data from Encyclopedia of DNA Elements (ENCODE), we report cell type and TF specific TF-cofactor interactions captured in vivo through enrichments of non target cofactor binding site motifs within ChIP-seq peaks. We observe enrichments in both known and novel cofactor motifs.

CONCLUSIONS

Given the regulatory implications which TF and cofactor interactions have on a cell's phenotype, their identification is necessary but challenging. Here we present the findings to our analyses surrounding the investigation of TF-cofactor interactions encoded within TF ChIP-seq peaks. Novel cofactor binding site enrichments observed provides valuable insight into TF and cell type specific interactions driving TF interactions.

摘要

背景

转录因子(TFs)与辅因子之间的细胞类型及TF特异性相互作用对于通过将通用转录机制招募至基因启动子区域进行转录调控至关重要,且其识别严重依赖于蛋白质相互作用检测。

结果

利用来自DNA元件百科全书(ENCODE)的TF靶向染色质免疫沉淀结合大规模平行测序(ChIP-seq)数据,我们报告了通过ChIP-seq峰内非靶标辅因子结合位点基序的富集在体内捕获的细胞类型及TF特异性TF-辅因子相互作用。我们在已知和新型辅因子基序中均观察到富集。

结论

鉴于TF与辅因子相互作用对细胞表型具有调控意义,其识别是必要的但具有挑战性。在此,我们展示围绕TF ChIP-seq峰内编码的TF-辅因子相互作用研究的分析结果。观察到的新型辅因子结合位点富集为驱动TF相互作用的TF和细胞类型特异性相互作用提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dce/3852067/8b4f524a43ef/1471-2164-14-S5-S2-1.jpg

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