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Physical Modeling of Dynamic Coupling between Chromosomal Loci

机译:染色体位点之间动态耦合的物理建模

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摘要

The motion of chromosomal DNA is essential to many biological processes, including segregation, transcriptional regulation, recombination, and packaging. Physical understanding of these processes would be dramatically enhanced through predictive, quantitative modeling of chromosome dynamics of multiple loci. Using a polymer dynamics framework, we develop a prediction for the correlation in the velocities of two loci on a single chromosome or otherwise connected by chromatin. These predictions reveal that the signature of correlated motion between two loci can be identified by varying the lag time between locus position measurements. In general, this theory predicts that as the lag time interval increases, the dual-loci dynamic behavior transitions from being completely uncorrelated to behaving as an effective single locus. This transition corresponds to the timescale of the stress communication between loci through the intervening segment. This relatively simple framework makes quantitative predictions based on a single timescale fit parameter that can be directly compared to the in vivo motion of fluorescently labeled chromosome loci. Furthermore, this theoretical framework enables the detection of dynamically coupled chromosome regions from the signature of their correlated motion.
机译:染色体DNA的运动对于许多生物过程至关重要,包括分离,转录调控,重组和包装。通过对多个基因座的染色体动力学进行预测,定量建模,可以大大增强对这些过程的物理理解。使用聚合物动力学框架,我们对单个染色体上或通过染色质连接的两个基因座的速度之间的相关性进行了预测。这些预测表明,可以通过改变基因座位置测量之间的滞后时间来识别两个基因座之间相关运动的特征。通常,该理论预测,随着滞后时间间隔的增加,双轨动态行为将从完全不相关的行为转变为有效的单轨行为。该过渡对应于通过插入段的基因座之间的应力通讯的时间尺度。这种相对简单的框架基于单个时标拟合参数进行定量预测,该参数可以直接与荧光标记的染色体基因座的体内运动进行比较。此外,这种理论框架使得能够根据相关运动的特征来检测动态耦合的染色体区域。

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