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Identification of cis-regulatory modules in promoters of human genes exploiting mutual positioning of transcription factors

机译:利用转录因子的相互定位鉴定人类基因启动子中的顺式调控模块

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摘要

In higher organisms, gene regulation is controlled by the interplay of non-random combinations of multiple transcription factors (TFs). Although numerous attempts have been made to identify these combinations, important details, such as mutual positioning of the factors that have an important role in the TF interplay, are still missing. The goal of the present work is in silico mapping of some of such associating factors based on their mutual positioning, using computational screening. We have selected the process of myogenesis as a study case, and we focused on TF combinations involving master myogenic TF Myogenic differentiation (MyoD) with other factors situated at specific distances from it. The results of our work show that some muscle-specificfactors occur together with MyoD within the range of +-100 bp in a large number of promoters. We confirm co-occurrence of the MyoD with muscle-specific factors as described in earlier studies. However, we have also found novel relationships of MyoD withother factors not specific for muscle. Additionally, we have observed that MyoD tends to associate with different factors in proximal and distal promoter areas. The major outcome of our study is establishing the genome-wide connection between biologicalinteractions of TFs and close co-occurrence of their binding sites.
机译:在高等生物中,基因调控由多种转录因子(TF)的非随机组合的相互作用控制。尽管已进行了许多尝试来识别这些组合,但是仍然缺少重要的细节,例如在TF相互作用中具有重要作用的因素的相互定位。本工作的目标是使用计算筛选,基于它们之间的相互定位,对某些这样的关联因素进行计算机映射。我们已选择肌发生过程作为研究案例,并且我们重点研究了涉及主要肌成因的TF组合TF肌成因分化(MyoD)以及距其特定距离的其他因素。我们的工作结果表明,在许多启动子中,某些肌肉特异性因子与MyoD一起出现在+ -100 bp的范围内。我们确认MyoD与特定于肌肉的因子同时存在,如先前的研究所述。但是,我们还发现了MyoD与肌肉特有的其他因素之间的新颖关系。此外,我们已经观察到MyoD倾向于与近端和远端启动子区域中的不同因素相关联。我们研究的主要结果是建立TFs的生物相互作用与其结合位点紧密共存之间的全基因组连接。

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