Chromatin as self-returning walks: From population to single cell and back.

IF 2.4 Q3 BIOPHYSICS Biophysical reports Pub Date : 2022-03-09 DOI:10.1016/j.bpr.2021.100042
Anne R Shim, Kai Huang, Vadim Backman, Igal Szleifer
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引用次数: 1

Abstract

With a growing understanding of the chromatin structure, many efforts remain focused on bridging the gap between what is suggested by population-averaged data and what is visualized for single cells. A popular approach to traversing these scales is to fit a polymer model to Hi-C contact data. However, Hi-C is an average of millions to billions of cells, and each cell may not contain all population-averaged contacts. Therefore, we employ a novel approach of summing individual chromosome trajectories-determined by our Self-Returning Random Walk model-to create populations of cells. We allow single cells to consist of disparate structures and reproduce a variety of experimentally relevant contact maps. We show that the amount of shared topology between cells, and their mechanism of formation, changes the population-averaged structure. Therefore, we present a modeling technique that, with few constraints and little oversight, can be used to understand which single-cell chromatin structures underlie population-averaged behavior.

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自我回归的染色质:从群体到单细胞再回来。
随着对染色质结构的理解不断加深,许多努力仍然集中在弥合人口平均数据和单细胞可视化数据之间的差距。一种流行的遍历这些尺度的方法是将聚合物模型拟合到Hi-C接触数据。然而,Hi-C是数百万到数十亿个细胞的平均值,每个细胞可能不包含所有的群体平均接触。因此,我们采用了一种新的方法,将个体染色体轨迹相加——由我们的自回归随机行走模型决定——来创建细胞群。我们允许单个细胞由不同的结构组成,并重现各种实验相关的接触图。我们展示了细胞之间共享拓扑的数量,以及它们的形成机制,改变了种群平均结构。因此,我们提出了一种建模技术,在很少的限制和很少的监督下,可以用来理解哪些单细胞染色质结构是群体平均行为的基础。
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来源期刊
Biophysical reports
Biophysical reports Biophysics
CiteScore
2.40
自引率
0.00%
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0
审稿时长
75 days
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