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首页> 外文期刊>Cell Reports >Cohesin-Dependent and -Independent Mechanisms Mediate Chromosomal Contacts between Promoters and Enhancers
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Cohesin-Dependent and -Independent Mechanisms Mediate Chromosomal Contacts between Promoters and Enhancers

机译:尼蛋白依赖性和依赖性机制介导启动子和增强剂之间的染色体接触

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It is currently assumed that 3D chromosomal organization plays a central role in transcriptional control. However, depletion of cohesin and CTCF affects the steady-state levels of only a minority of transcripts. Here, we use high-resolution Capture Hi-C to interrogate the dynamics of chromosomal contacts of all annotated human gene promoters upon degradation of cohesin and CTCF . We show that a majority of promoter-anchored contacts are lost in these conditions, but many contacts with distinct properties are maintained, and some new ones are gained. The rewiring of contacts between promoters and active enhancers upon cohesin degradation associates with rapid changes in target gene transcription as detected by SLAM sequencing (SLAM-seq). These results provide a mechanistic explanation for the limited, but consistent, effects of cohesin and CTCF depletion on steady-state transcription and suggest the existence of both cohesin-dependent and -independent mechanisms of enhancer-promoter pairing.
机译:目前假设3D染色体组织在转录控制中起着核心作用。然而,休谷蛋白和CTCF的耗尽影响了仅少数成绩单的稳态水平。在这里,我们使用高分辨率捕获HI-C在降解COLEN和CTCF时询问所有注释的人类基因启动子的染色体触点的动态。我们表明,在这些条件下,大多数启动子锚定触点丢失,但维持了许多具有不同性质的触点,并且获得了一些新的触点。在Cohyin降解时,启动子和活性增强子之间的接触的再次促进与SLAM测序(SLAM-SEQ)检测到的靶基因转录的快速变化。这些结果为有限的幼耳和CTCF耗尽对稳态转录提供了有限但一致,效果的机械解释,并表明了增强剂 - 启动子配对的依尼蛋白依赖性和依赖性机制的存在。

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