Retrospective and multifactorial single-cell profiling reveals sequential chromatin reorganization during X inactivation

IF 19.1 1区 生物学 Q1 CELL BIOLOGY
Samy Kefalopoulou, Pim M. J. Rullens, Kim L. de Luca, Sandra S. de Vries, Tessy Korthout, Alexander van Oudenaarden, Peter Zeller, Jop Kind
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Abstract

The regulation of gene expression is governed at multiple levels of chromatin organization. However, how gene regulation is co-ordinated remains relatively unexplored. Here we develop Dam&ChIC, a method that enables retrospective and multifactorial chromatin profiling in single cells. Dam&ChIC employs chromatin labelling in living cells with m6A to acquire a past chromatin state, coupled with an antibody-mediated readout to capture the present chromatin state. Analyses of diverse factor combinations highlight its versatility and superior resolution. By tracking lamina-associated domain inheritance over the cell cycle, we showcase that Dam&ChIC provides retrospective single-cell chromatin data. When applied in random X chromosome inactivation, Dam&ChIC disentangles the temporal order of chromatin remodelling events. Upon mitotic exit and following Xist expression, the inactive X chromosome undergoes extensive genome–lamina detachment, preceding spreading of Polycomb. We anticipate that Dam&ChIC will be instrumental in unravelling the interconnectivity and order of gene-regulatory events underlying cell-state changes during development.

Abstract Image

回顾性和多因子单细胞分析揭示了X失活过程中染色质的顺序重组
基因表达的调控是在染色质组织的多个水平上进行的。然而,基因调控是如何协调的仍未被探索。在这里,我们开发Dam&;ChIC,一种在单个细胞中进行回顾性和多因子染色质分析的方法。Dam&;ChIC在带有m6A的活细胞中使用染色质标记来获得过去的染色质状态,再加上抗体介导的读数来捕获当前的染色质状态。多种因子组合的分析突出了其通用性和优越的分辨率。通过在细胞周期中跟踪层相关结构域遗传,我们发现Dam&;ChIC提供了回溯性的单细胞染色质数据。当应用于随机X染色体失活时,Dam&;ChIC解开了染色质重塑事件的时间顺序。在有丝分裂结束后,随着Xist的表达,失活的X染色体经历了广泛的基因组-膜分离,在Polycomb扩散之前。我们预计,Dam&;ChIC将有助于揭示发育过程中细胞状态变化背后的基因调控事件的互联性和顺序。
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来源期刊
Nature Cell Biology
Nature Cell Biology 生物-细胞生物学
CiteScore
28.40
自引率
0.90%
发文量
219
审稿时长
3 months
期刊介绍: Nature Cell Biology, a prestigious journal, upholds a commitment to publishing papers of the highest quality across all areas of cell biology, with a particular focus on elucidating mechanisms underlying fundamental cell biological processes. The journal's broad scope encompasses various areas of interest, including but not limited to: -Autophagy -Cancer biology -Cell adhesion and migration -Cell cycle and growth -Cell death -Chromatin and epigenetics -Cytoskeletal dynamics -Developmental biology -DNA replication and repair -Mechanisms of human disease -Mechanobiology -Membrane traffic and dynamics -Metabolism -Nuclear organization and dynamics -Organelle biology -Proteolysis and quality control -RNA biology -Signal transduction -Stem cell biology
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