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通过 DNA 聚合体序列依赖性变形实现核小体定位的分子进化。

The molecular evolution of nucleosome positioning through sequence-dependent deformation of the DNA polymer.

机构信息

School of Biological and Medical Sciences, Rochester Institute of Technology, Rochester, NY, USA.

出版信息

J Biomol Struct Dyn. 2010 Jun;27(6):765-80. doi: 10.1080/07391102.2010.10508584.

Abstract

The computational prediction of nucleosome positioning from DNA sequence now allows for in silico investigation of the molecular evolution of biophysical properties of the DNA molecule responsible for primary chromatin organization in the genome. To discern what signal components driving nucleosome positioning in the yeast genome are potentially targeted by natural selection, we compare the performance of various models predictive of nucleosome positioning within the context of a simple statistical test, the repositioned mutation test. We demonstrate that while nucleosome occupancy is driven largely by translational exclusion in response to AT content, there is also a strong signature of evolutionary conservation of regular patterns within nucleosomal DNA sequence related to the structural organization of the nucleosome core (e.g., 10-bp dinucleotide periodicity). We also use computer simulations to investigate hypothetical coding and regulatory constraints on the ability of sequence properties affecting nucleosome formation to adaptively evolve. Our results demonstrate that natural selection may act independently on different DNA sequence properties responsible for local chromatin organization. Furthermore, at least with respect to the deformation energy of the DNA molecule in the nucleosome, the presence of the genetic code has greatly restricted the ability of sequences to evolve the dynamic nucleosome organization typically observed in promoter regions.

摘要

现在,从 DNA 序列计算预测核小体定位使得人们可以在计算机上研究负责基因组中初级染色质组织的 DNA 分子的生物物理性质的分子进化。为了辨别哪些信号成分可能是自然选择针对的,驱动酵母基因组中的核小体定位,我们在一个简单的统计测试——重定位突变测试的背景下比较了各种核小体定位预测模型的性能。我们证明,尽管核小体占有率主要是由于 AT 含量的平移排斥驱动的,但核小体 DNA 序列中也存在与核小体核心结构组织(例如,10 个碱基对二核苷酸周期性)相关的规则模式的进化保守性的强烈特征。我们还使用计算机模拟来研究影响核小体形成的序列特性对适应性进化的编码和调控限制的假设。我们的结果表明,自然选择可能独立于负责局部染色质组织的不同 DNA 序列特性起作用。此外,至少就核小体中 DNA 分子的变形能而言,遗传密码的存在极大地限制了序列进化通常在启动子区域观察到的动态核小体组织的能力。

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