Quantifying the large-scale chromosome structural dynamics during the mitosis-to-G1 phase transition of cell cycle

Author:

Chu XiakunORCID,Wang Jin

Abstract

AbstractCell cycle, essential for various cellular processes, is known to be precisely regulated by the underlying gene network. Accumulating evidence has revealed that the chromosome, which serves as the scaffold for the gene expressions, undergoes significant structural reorganizations during mitosis. Understanding the mechanism of the cell cycle from the molecular chromosome structural perspective remains a grand challenge. In this study, we applied an integrated approach using a data-driven model combined with a nonequilibrium landscape-switching model to investigate large-scale chromosome structural dynamics during the mitosis-to-G1 phase transition. We generated 3D chromosome structural ensembles for the five critical stages in the process. We observed that the chromosome structural expansion and adaptation of the structural asphericity do not occur synchronously. We attributed this asynchronous adaptation behavior in the chromosome structural geometry to the unique unloading sequence of the two types of condensins. Furthermore, we observed that the coherent motions between the chromosomal loci are primarily enhanced within the topologically associating domains (TADs) as cells progress to the G1 phase, suggesting that TADs can be considered as both structural and dynamical units for organizing the 3D chromosome. Our analysis also reveals that the quantified pathways of chromosome structural reorganizations during the mitosis-to-G1 phase transition exhibit high stochasticity at the single-cell level and show non-linear behaviors in changing TADs and contacts formed at the long-range regions. These features underscore the complex nature of the cell-cycle processes. Our findings, which are consistent with the experiments in many aspects, offer valuable insights into the large-scale chromosome structural dynamics after mitosis and contribute to the molecular-level understanding of the cell-cycle process.

Publisher

Cold Spring Harbor Laboratory

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3