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预测基因组中的核小体定位:物理和生物信息学方法。

Predicting nucleosome positioning in genomes: physical and bioinformatic approaches.

机构信息

Dipartimento di Chimica, Università di Roma La Sapienza, P.le A. Moro, 5 I-00185, Roma, Italy.

出版信息

Biophys Chem. 2011 May;155(2-3):53-64. doi: 10.1016/j.bpc.2011.03.006. Epub 2011 Apr 9.

DOI:10.1016/j.bpc.2011.03.006
PMID:21482020
Abstract

In eukaryotic genomes, nucleosomes are responsible for packaging DNA and controlling gene expression. For this reason, an increasing interest is arising on computational methods capable of predicting the nucleosome positioning along genomes. In this review we describe and compare bioinformatic and physical approaches adopted to predict nucleosome occupancy along genomes. Computational analyses attempt at decoding the experimental nucleosome maps of genomes in terms of certain dinucleotide step periodicity observed along DNA. Such investigations show that highly significant information about the occurrence of a nucleosome along DNA is intrinsic in certain features of the sequence suggesting that DNA of eukaryotic genomes encodes nucleosome organization. Besides the bioinformatic approaches, physical models were proposed based on the sequence dependent conformational features of the DNA chain, which govern the free energy needed to transform recurrent DNA tracts along the genome into the nucleosomal shape.

摘要

在真核生物基因组中,核小体负责包装 DNA 并控制基因表达。因此,人们对能够预测基因组中核小体定位的计算方法越来越感兴趣。在这篇综述中,我们描述并比较了用于预测基因组中核小体占有率的生物信息学和物理方法。计算分析试图根据 DNA 上观察到的特定二核苷酸步周期性,对基因组的实验核小体图谱进行解码。这些研究表明,在 DNA 上发生核小体的特定序列特征中固有地包含了有关核小体在 DNA 上出现的高度显著信息,这表明真核生物基因组的 DNA 编码核小体组织。除了生物信息学方法之外,还基于 DNA 链的序列依赖性构象特征提出了物理模型,这些模型控制了将基因组中反复出现的 DNA 片段转化为核小体形状所需的自由能。

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1
Predicting nucleosome positioning in genomes: physical and bioinformatic approaches.预测基因组中的核小体定位:物理和生物信息学方法。
Biophys Chem. 2011 May;155(2-3):53-64. doi: 10.1016/j.bpc.2011.03.006. Epub 2011 Apr 9.
2
Prediction of nucleosome positioning in genomes: limits and perspectives of physical and bioinformatic approaches.基因组中核小体定位的预测:物理和生物信息学方法的局限性和展望。
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A statistical thermodynamic approach for predicting the sequence-dependent nucleosome positioning along genomes.一种基于统计热力学的方法,用于预测基因组中序列依赖性核小体定位。
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Long-range correlations between DNA bending sites: relation to the structure and dynamics of nucleosomes.DNA弯曲位点之间的长程相关性:与核小体结构和动力学的关系。
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Computational analysis suggests a highly bendable, fragile structure for nucleosomal DNA.计算分析表明核小体 DNA 具有高度可弯曲、脆弱的结构。
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Sequence-dependent nucleosome positioning.序列依赖性核小体定位
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引用本文的文献

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Consecutive low-frequency shifts in A/T content denote nucleosome positions across microeukaryotes.A/T含量的连续低频变化表明了微真核生物中的核小体位置。
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Galaxy Dnpatterntools for Computational Analysis of Nucleosome Positioning Sequence Patterns.星系 Dnpatterntools 用于核小体定位序列模式的计算分析。
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Coupling between Sequence-Mediated Nucleosome Organization and Genome Evolution.
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Nucleosome positioning sequence patterns as packing or regulatory.核小体定位序列模式作为包装或调节。
PLoS Comput Biol. 2020 Jan 27;16(1):e1007365. doi: 10.1371/journal.pcbi.1007365. eCollection 2020 Jan.
5
The implication of DNA bending energy for nucleosome positioning and sliding.DNA 弯曲能对核小体定位和滑动的影响。
Sci Rep. 2018 Jun 11;8(1):8853. doi: 10.1038/s41598-018-27247-x.
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A deformation energy-based model for predicting nucleosome dyads and occupancy.一种基于变形能量的预测核小体二分体和占有率的模型。
Sci Rep. 2016 Apr 7;6:24133. doi: 10.1038/srep24133.
7
Fuzziness and noise in nucleosomal architecture.核小体结构中的模糊性和噪声。
Nucleic Acids Res. 2014 Apr;42(8):4934-46. doi: 10.1093/nar/gku165. Epub 2014 Feb 27.