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本文引用的文献

1
High order chromatin architecture shapes the landscape of chromosomal alterations in cancer.高级染色质结构塑造了癌症中染色体改变的景观。
Nat Biotechnol. 2011 Nov 20;29(12):1109-13. doi: 10.1038/nbt.2049.
2
The three-dimensional architecture of a bacterial genome and its alteration by genetic perturbation.细菌基因组的三维结构及其遗传扰动的改变。
Mol Cell. 2011 Oct 21;44(2):252-64. doi: 10.1016/j.molcel.2011.09.010.
3
A model for Escherichia coli chromosome packaging supports transcription factor-induced DNA domain formation.大肠杆菌染色体包装模型支持转录因子诱导的 DNA 域形成。
Nucleic Acids Res. 2012 Feb;40(3):972-80. doi: 10.1093/nar/gkr779. Epub 2011 Oct 5.
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Genome-wide translocation sequencing reveals mechanisms of chromosome breaks and rearrangements in B cells.全基因组易位测序揭示了 B 细胞中染色体断裂和重排的机制。
Cell. 2011 Sep 30;147(1):107-19. doi: 10.1016/j.cell.2011.07.049.
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Translocation-capture sequencing reveals the extent and nature of chromosomal rearrangements in B lymphocytes.易位捕获测序揭示了 B 淋巴细胞中染色体重排的程度和性质。
Cell. 2011 Sep 30;147(1):95-106. doi: 10.1016/j.cell.2011.07.048.
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Bridging the resolution gap in structural modeling of 3D genome organization.弥合 3D 基因组组织结构建模分辨率差距。
PLoS Comput Biol. 2011 Jul;7(7):e1002125. doi: 10.1371/journal.pcbi.1002125. Epub 2011 Jul 14.
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Variegated gene expression caused by cell-specific long-range DNA interactions.由细胞特异性长程 DNA 相互作用引起的基因表达多样化。
Nat Cell Biol. 2011 Jun 26;13(8):944-51. doi: 10.1038/ncb2278.
8
Molecular dynamics simulation study of nonconcatenated ring polymers in a melt. II. Dynamics.无规线团聚合物熔体的分子动力学模拟研究。Ⅱ.动力学。
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9
Principles of chromosomal organization: lessons from yeast.染色体组织的原则:来自酵母的启示。
J Cell Biol. 2011 Mar 7;192(5):723-33. doi: 10.1083/jcb.201010058.
10
4D chromatin dynamics in cycling cells: Theodor Boveri's hypotheses revisited.有丝分裂细胞中的 4D 染色质动力学:重温 Theodor Boveri 的假说。
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高级染色质结构:连接物理与生物学。

Higher-order chromatin structure: bridging physics and biology.

机构信息

Graduate Program in Biophysics, Harvard University, Cambridge, MA, United States.

出版信息

Curr Opin Genet Dev. 2012 Apr;22(2):115-24. doi: 10.1016/j.gde.2012.01.006. Epub 2012 Feb 22.

DOI:10.1016/j.gde.2012.01.006
PMID:22360992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3697851/
Abstract

Advances in microscopy and genomic techniques have provided new insight into spatial chromatin organization inside of the nucleus. In particular, chromosome conformation capture data has highlighted the relevance of polymer physics for high-order chromatin organization. In this context, we review basic polymer states, discuss how an appropriate polymer model can be determined from experimental data, and examine the success and limitations of various polymer models of higher-order interphase chromatin organization. By taking into account topological constraints acting on the chromatin fiber, recently developed polymer models of interphase chromatin can reproduce the observed scaling of distances between genomic loci, chromosomal territories, and probabilities of contacts between loci measured by chromosome conformation capture methods. Polymer models provide a framework for the interpretation of experimental data as ensembles of conformations rather than collections of loops, and will be crucial for untangling functional implications of chromosomal organization.

摘要

显微镜技术和基因组技术的进步为核内空间染色质组织提供了新的见解。特别是,染色体构象捕获数据强调了高分子物理对于高级染色质组织的重要性。在这种情况下,我们回顾了基本的聚合物状态,讨论了如何从实验数据中确定合适的聚合物模型,并研究了各种高级相间染色质组织的聚合物模型的成功和局限性。通过考虑作用在染色质纤维上的拓扑约束,最近开发的相间染色质聚合物模型可以再现通过染色体构象捕获方法测量的基因组位点、染色体区域之间的距离以及位点之间接触概率的观察到的标度。聚合物模型为解释实验数据提供了一个框架,即将其作为构象的集合而不是环的集合,对于梳理染色体组织的功能意义至关重要。