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Feedback enrichment analysis for transcription factor-target genes in signaling pathways

机译:信号通路中转录因子靶基因的反馈富集分析

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摘要

Feedback regulation plays an important role in the regulation of molecular processes. Although feedback regulatory mechanisms that generate potential-specific dynamic behavior, such as oscillation and switch-like activation, have been found, their significant contribution to the signal transduction system has not been fully explored. In this study, I focused on the feedback regulation of signal molecules like transcription factor (TF)-associated target genes controlled after transcription (named TF-target feedback genes). I statistically analyzed the static network of signal transduction pathways and TF-target feedbacks to investigate their presence in upstream signal molecules of TFs in 394 different cell types, including 146 primary cells, 111 tissues, and 137 cell lines. The directed network of signal transduction utilized pathways annotated in KEGG, and the TF-target genes estimated per individual cells were used. Feedback enrichment analysis of upstream signal molecules of TF was performed to investigate whether TF-target genes are upstream of their TF and form a feedback loop in signal transduction. The study revealed the difference in the number of TF-target feedbacks between cells, while each cell had at least 11 significant TF-target feedbacks and invariably involved the E2F transcription factor 4 feedback within the cell cycle. The findings suggest the possibility of the regulation of the TF-associated signal transduction by the TF itself at the transcription level.
机译:反馈监管在分子过程的调节中起着重要作用。尽管已经发现了产生潜在特异性动态行为的反馈监管机制,例如振荡和交换机的激活,但它们对信号转导系统的显着贡献尚未得到充分探索。在该研究中,我专注于转录后(TF) - 分类的靶基因等信号分子的反馈调节(命名为TF-靶反馈基因)。我在统计上分析了信号转导途径和TF-靶反馈的静态网络,以研究其在394种不同细胞类型中的TFS上游信号分子中的存在,包括146种主要细胞,111个组织和137个细胞系。使用在kegg中注释的信号转导使用途径的定向网络,并使用每种细胞估计的TF-靶基因。进行TF的上游信号分子的反馈富集分析以研究TF-靶基因是否在其TF的上游,并在信号转导中形成反馈环。该研究揭示了细胞之间的TF-靶反馈的数量的差异,而每个细胞具有至少11个显着的TF-靶反馈,并且总是涉及细胞周期内的E2F转录因子4反馈。研究结果表明,TF本身在转录水平上调节TF相关信号转导的可能性。

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