Tianyu YuanIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Physics, Yale University, New Haven, Connecticut, USA, Hao YanIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Physics, Yale University, New Haven, Connecticut, USA, Mary Lou P. BaileyIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Applied Physics, Yale University, New Haven, Connecticut, USA, Jessica F. WilliamsDepartment of Cell Biology, Yale School of Medicine, New Haven, Connecticut, USA, Ivan SurovtsevDepartment of Physics, Yale University, New Haven, Connecticut, USADepartment of Cell Biology, Yale School of Medicine, New Haven, Connecticut, USA, Megan C. KingIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Cell Biology, Yale School of Medicine, New Haven, Connecticut, USADepartment of Molecular, Cell and Developmental Biology, Yale University, New Haven, Connecticut, USA, Simon G. J. MochrieIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Physics, Yale University, New Haven, Connecticut, USADepartment of Applied Physics, Yale University, New Haven, Connecticut, USA
{"title":"The effect of loops on the mean square displacement of Rouse-model chromatin","authors":"Tianyu YuanIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Physics, Yale University, New Haven, Connecticut, USA, Hao YanIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Physics, Yale University, New Haven, Connecticut, USA, Mary Lou P. BaileyIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Applied Physics, Yale University, New Haven, Connecticut, USA, Jessica F. WilliamsDepartment of Cell Biology, Yale School of Medicine, New Haven, Connecticut, USA, Ivan SurovtsevDepartment of Physics, Yale University, New Haven, Connecticut, USADepartment of Cell Biology, Yale School of Medicine, New Haven, Connecticut, USA, Megan C. KingIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Cell Biology, Yale School of Medicine, New Haven, Connecticut, USADepartment of Molecular, Cell and Developmental Biology, Yale University, New Haven, Connecticut, USA, Simon G. J. MochrieIntegrated Graduate Program in Physical and Engineering Biology, Yale University, New Haven, Connecticut, USADepartment of Physics, Yale University, New Haven, Connecticut, USADepartment of Applied Physics, Yale University, New Haven, Connecticut, USA","doi":"arxiv-2304.11266","DOIUrl":null,"url":null,"abstract":"Many researchers have been encouraged to describe the dynamics of chromosomal\nloci in chromatin using the classical Rouse model of polymer dynamics by the\nagreement between the measured mean square displacement (MSD) versus time of\nfluorescently-labelled loci and the Rouse-model predictions. However, the\ndiscovery of intermediate-scale chromatin organization, known as topologically\nassociating domains (TADs), together with the proposed explanation of TADs in\nterms of chromatin loops and loop extrusion, is at odds with the classical\nRouse model, which does not contain loops. Accordingly, we introduce an\nextended Rouse model that incorporates chromatin loop configurations from\nloop-extrusion-factor-model simulations. Specifically, we extend the classical\nRouse model by modifying the polymer's dynamical matrix to incorporate extra\nsprings that represent loop bases. We also theoretically generalize the\nfriction coefficient matrix so that the Rouse beads with non-uniform friction\ncoefficients are compatible with our Rouse model simulation method. This\nextended Rouse model allowes us to investigate the impact of loops and loop\nextrusion on the dynamics of chromatin. We show that loops significantly\nsuppress the averaged MSD of a chromosomal locus, consistent with recent\nexperiments that track fluorescently-labelled chromatin loci in fission yeast\n[M. L. P. Bailey, I. Surovtsev, J. F. Williams, H. Yan, T. Yuan, S. G. Mochrie,\nand M. C. King, Mol. Biol. Cell (in press)]. We also find that loops slightly\nreduce the MSD's stretching exponent from the classical Rouse-model value of\n0.5 to a loop-density-dependent value in the 0.45-0.40 range. Remarkably,\nstretching exponent values in this range have also been reported in recent\nexperiments [S. C. Weber, A. J. Spakowitz, and J. A. Theriot, Phys. Rev. Lett.\n104, 238102 (2010) and Bailey et al., Mol. Biol. Cell (in press)].","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"185 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Subcellular Processes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2304.11266","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Many researchers have been encouraged to describe the dynamics of chromosomal
loci in chromatin using the classical Rouse model of polymer dynamics by the
agreement between the measured mean square displacement (MSD) versus time of
fluorescently-labelled loci and the Rouse-model predictions. However, the
discovery of intermediate-scale chromatin organization, known as topologically
associating domains (TADs), together with the proposed explanation of TADs in
terms of chromatin loops and loop extrusion, is at odds with the classical
Rouse model, which does not contain loops. Accordingly, we introduce an
extended Rouse model that incorporates chromatin loop configurations from
loop-extrusion-factor-model simulations. Specifically, we extend the classical
Rouse model by modifying the polymer's dynamical matrix to incorporate extra
springs that represent loop bases. We also theoretically generalize the
friction coefficient matrix so that the Rouse beads with non-uniform friction
coefficients are compatible with our Rouse model simulation method. This
extended Rouse model allowes us to investigate the impact of loops and loop
extrusion on the dynamics of chromatin. We show that loops significantly
suppress the averaged MSD of a chromosomal locus, consistent with recent
experiments that track fluorescently-labelled chromatin loci in fission yeast
[M. L. P. Bailey, I. Surovtsev, J. F. Williams, H. Yan, T. Yuan, S. G. Mochrie,
and M. C. King, Mol. Biol. Cell (in press)]. We also find that loops slightly
reduce the MSD's stretching exponent from the classical Rouse-model value of
0.5 to a loop-density-dependent value in the 0.45-0.40 range. Remarkably,
stretching exponent values in this range have also been reported in recent
experiments [S. C. Weber, A. J. Spakowitz, and J. A. Theriot, Phys. Rev. Lett.
104, 238102 (2010) and Bailey et al., Mol. Biol. Cell (in press)].
由于测量的均方位移(MSD)与时间荧光标记的位点之间的一致,许多研究人员被鼓励使用经典的聚合物动力学rose模型来描述染色质中染色体座的动力学。然而,被称为拓扑相关结构域(TADs)的中尺度染色质组织的发现,以及对TADs在染色质环和环挤压方面的解释,与经典的不包含环的rouse模型不一致。因此,我们引入了一个扩展的劳斯模型,该模型结合了环挤压因子模型模拟的染色质环结构。具体来说,我们通过修改聚合物的动态矩阵来扩展经典的rouse模型,以纳入代表环基的外弹簧。我们还从理论上推广了摩擦系数矩阵,使得具有非均匀摩擦系数的劳斯微珠与我们的劳斯模型模拟方法兼容。这种扩展的劳斯模型使我们能够研究环和环挤压对染色质动力学的影响。我们发现环路显著抑制染色体位点的平均MSD,这与最近在裂变酵母中跟踪荧光标记的染色质位点的实验一致。L. P. Bailey, I. Surovtsev, J. F. Williams, H. Yan, T. Yuan, S. G. Mochrie, M. C. King, Mol. Biol。单元格(按下)]。我们还发现,循环将MSD的拉伸指数从经典的劳斯模型值0.5略微降低到0.45-0.40范围内与循环密度相关的值。值得注意的是,在最近的实验中也报道了在这个范围内拉伸指数值[S]。C. Weber, A. J. Spakowitz,和J. A. Theriot,物理学。Rev. letters .104, 238102 (2010) and Bailey et al., Mol. Biol。单元格(按下)]。