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本文引用的文献

1
Entropy as the driver of chromosome segregation.熵作为染色体分离的驱动力。
Nat Rev Microbiol. 2010 Aug;8(8):600-7. doi: 10.1038/nrmicro2391.
2
Interplay between writhe and knotting for swollen and compact polymers.肿胀和紧致聚合物的扭绞和打结之间的相互作用。
J Chem Phys. 2009 Oct 21;131(15):154902. doi: 10.1063/1.3244643.
3
Strong intranucleoid interactions organize the Escherichia coli chromosome into a nucleoid filament.强烈的核内相互作用将大肠杆菌染色体组织成核纤丝。
Proc Natl Acad Sci U S A. 2010 Mar 16;107(11):4991-5. doi: 10.1073/pnas.0912062107. Epub 2010 Mar 1.
4
DNA-DNA interactions in bacteriophage capsids are responsible for the observed DNA knotting.噬菌体衣壳中的 DNA-DNA 相互作用是造成观察到的 DNA 扭结的原因。
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22269-74. doi: 10.1073/pnas.0907524106. Epub 2009 Dec 14.
5
Entropic organization of interphase chromosomes.间期染色体的熵组织
J Cell Biol. 2009 Sep 21;186(6):825-34. doi: 10.1083/jcb.200903083. Epub 2009 Sep 14.
6
Topological origins of chromosomal territories.染色体领地的拓扑起源。
Nucleic Acids Res. 2009 Oct;37(19):6316-22. doi: 10.1093/nar/gkp702. Epub 2009 Sep 2.
7
Protein occupancy landscape of a bacterial genome.细菌基因组的蛋白质占据图谱。
Mol Cell. 2009 Jul 31;35(2):247-53. doi: 10.1016/j.molcel.2009.06.035.
8
Linking topology of tethered polymer rings with applications to chromosome segregation and estimation of the knotting length.将拴系聚合物环的拓扑结构与染色体分离应用及打结长度估计联系起来。
Phys Rev E Stat Nonlin Soft Matter Phys. 2009 May;79(5 Pt 1):051905. doi: 10.1103/PhysRevE.79.051905. Epub 2009 May 11.
9
Non-specific interactions are sufficient to explain the position of heterochromatic chromocenters and nucleoli in interphase nuclei.非特异性相互作用足以解释异染色质染色中心和核仁在间期细胞核中的位置。
Nucleic Acids Res. 2009 Jun;37(11):3558-68. doi: 10.1093/nar/gkp219. Epub 2009 Apr 9.
10
Structure and dynamics of interphase chromosomes.间期染色体的结构与动态变化
PLoS Comput Biol. 2008 Aug 22;4(8):e1000153. doi: 10.1371/journal.pcbi.1000153.

球形受限且拓扑平衡的柔性聚合物的连环数和扭曲数的标度

Scaling of Linking and Writhing Numbers for Spherically Confined and Topologically Equilibrated Flexible Polymers.

作者信息

Marko John F

机构信息

Department of Physics and Astronomy and Department of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA.

出版信息

J Stat Phys. 2011 Apr;142(6):1353-1370. doi: 10.1007/s10955-011-0172-4.

DOI:10.1007/s10955-011-0172-4
PMID:21686050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3115200/
Abstract

Scaling laws for Gauss linking number Ca and writhing number Wr for spherically confined flexible polymers with thermally fluctuating topology are analyzed. For ideal (phantom) polymers each of N segments of length unity confined to a spherical pore of radius R there are two scaling regimes: for sufficiently weak confinement (R ⪢ N(1/3)) each chain has |Wr| ≈ N(1/2), and each pair of chains has average |Ca| ≈ N/R(3/2); alternately for sufficiently tight confinement (N(1/3) ⪢ R), |Wr| ≈ |CA| ≈ N/R(3/2). Adding segment-segment avoidance modifies this result: for n chains with excluded volume interactions |Ca| ≈ (N/n)(1/2)f(ϕ) where f is a scaling function that depends approximately linearly on the segment concentration ϕ = nN/R(3). Scaling results for writhe are used to estimate the maximum writhe of a polymer; this is demonstrated to be realizable through a writhing instability that occurs for a polymer which is able to change knotting topology and which is subject to an applied torque. Finally, scaling results for linking are used to estimate bounds on the entanglement complexity of long chromosomal DNA molecules inside cells, and to show how "lengthwise" chromosome condensation can suppress DNA entanglement.

摘要

分析了具有热涨落拓扑结构的球形受限柔性聚合物的高斯链环数(Ca)和扭曲数(Wr)的标度律。对于理想(虚设)聚合物,长度为单位长度的(N)个链段中的每一个都被限制在半径为(R)的球形孔中,存在两种标度区域:对于足够弱的限制((R\gg N^{1/3})),每个链的(\vert Wr\vert\approx N^{1/2}),并且每对链的平均(\vert Ca\vert\approx N/R^{3/2});相反,对于足够强的限制((N^{1/3}\gg R)),(\vert Wr\vert\approx\vert CA\vert\approx N/R^{3/2})。添加链段-链段排斥会改变这个结果:对于具有排除体积相互作用的(n)条链,(\vert Ca\vert\approx (N/n)^{1/2}f(\phi)),其中(f)是一个标度函数,它大致线性地依赖于链段浓度(\phi = nN/R^{3})。扭曲的标度结果用于估计聚合物的最大扭曲;这被证明可以通过一种扭曲不稳定性来实现,这种不稳定性发生在能够改变打结拓扑结构并且受到外加扭矩的聚合物中。最后,链环的标度结果用于估计细胞内长染色体DNA分子的缠结复杂度的界限,并展示“纵向”染色体凝聚如何抑制DNA缠结。