首页> 外文会议>Bioinformatics Research and Applications; Lecture Notes in Bioinformatics; 4463 >DNA Sites Buried in Nucleosome Become Accessible at Room Temperature: A Discrete-Event-Simulation Based Modeling Approach
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DNA Sites Buried in Nucleosome Become Accessible at Room Temperature: A Discrete-Event-Simulation Based Modeling Approach

机译:埋藏在核小体中的DNA位点在室温下变得可访问:基于离散事件模拟的建模方法

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Conformation of a canonical nucleosome inhibits the direct access of the binding proteins to portions of nucleosomal DNA. Nucleosome dynamics establish certain pathways through which nucleosome gets remodeled (spontaneously, covalently or non-covalently) and the buried DNA sites become accessible. Currently for most pathways no single model is available to capture the temporal behavior of these pathways. Plus traditional diffusion-based models in most cases are not precise. In this work we have given a systematic overview of such pathways. Then, we manipulate the probability of a binding site on array of N nucleosomes and chromatin of length G base pairs . We further identify three of the widely accepted thermal-driven (passive) pathways and model those based on stochastic process and the Discrete-Event-Simulation. For the output of the models we have sought either the site access rate or the sliding rate of the nucleosome. We also show that results from these models match the experimental data where available.
机译:典型核小体的构象抑制了结合蛋白直接进入核小体DNA的部分。核小体动力学建立了某些途径,核小体可以通过该途径进行重塑(自发,共价或非共价),并且可以进入被掩埋的DNA位点。当前,对于大多数路径,没有一个单独的模型可用来捕获这些路径的时间行为。再加上传统的基于扩散的模型在大多数情况下并不精确。在这项工作中,我们对这些途径进行了系统的概述。然后,我们操纵长度为G个碱基对的N个核小体和染色质阵列上结合位点的概率。我们进一步确定了三种广为接受的热驱动(被动)路径,并基于随机过程和离散事件模拟对这些路径进行了建模。对于模型的输出,我们寻求了核小体的位点进入率或滑动率。我们还显示,这些模型的结果与可用的实验数据相匹配。

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