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Regulatory Domains and Their Mechanisms

机译:监管领域及其机制

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摘要

The concept of gene regulation is being refined as our understanding of the role of enhancer elements grows. Although described more than 30 years ago, the mechanisms through which these cis-regulating elements operate remain under debate. With the recognition that most of the human genetic variation contributing to common disease risk lies outside of genes and probably in cnhanccrs, unraveling these mechanisms becomes ever more important. Originally, a popular view was to consider regulatory elements as an entry site for the transcription machinery that could scan the intervening chromatin until the cognate core promoter was located. Now, the most prominent model for distal enhancer-promoter interaction involves direct enhancer/promoter contacts with a looping out of intervening chromatin. However, a rising awareness of the importance of chromatin architecture and organization forces us to consider enhancer-promoter communication in light of the polymer folding properties of chromatin. Here, we discuss how three-dimensional chromatin folding, topological domains, and the constrained motion, plasticity, and accessibility of chromatin could offer a structural basis for regulatory domains that greatly enhances the probability of enhancer-promoter and transcription factor-promoter interactions and gene activation.
机译:基因调节的概念正在精制,因为我们对增强子元素的作用增长的理解。虽然在30多年前描述了超过30年,但这些CIS调节因素经营的机制仍然在辩论下。据认识到大多数人类遗传变异导致常见疾病风险的变化在于基因外,可能在CNHANCCRS之外,解开这些机制变得更加重要。最初,普遍的观点是考虑监管要素作为可以扫描干预染色质的转录机械的进入部位,直到同源核心启动子位于所在的过程中。现在,最突出的远端增强剂 - 启动子相互作用模型涉及直接增强剂/启动子接触与中间染色质的循环。然而,对染色质建筑和组织的重要性的认识迫使我们根据染色质的聚合物折叠性能考虑增强剂 - 启动子通信。在这里,我们讨论了三维染色质折叠,拓扑结构域和染色质的受阻运动,可塑性和可移性如何为调节结构域提供大大提高增强剂 - 启动子和转录因子 - 启动子相互作用和基因的可能性的结构基础激活。

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