Computational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, 15213, PA, USA.
Oncode Institute and Division of Gene Regulation, Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, 1066 CX, The Netherlands.
Genome Biol. 2021 Jan 14;22(1):36. doi: 10.1186/s13059-020-02253-3.
We report SPIN, an integrative computational method to reveal genome-wide intranuclear chromosome positioning and nuclear compartmentalization relative to multiple nuclear structures, which are pivotal for modulating genome function. As a proof-of-principle, we use SPIN to integrate nuclear compartment mapping (TSA-seq and DamID) and chromatin interaction data (Hi-C) from K562 cells to identify 10 spatial compartmentalization states genome-wide relative to nuclear speckles, lamina, and putative associations with nucleoli. These SPIN states show novel patterns of genome spatial organization and their relation to other 3D genome features and genome function (transcription and replication timing). SPIN provides critical insights into nuclear spatial and functional compartmentalization.
我们报告了 SPIN,这是一种整合的计算方法,可以揭示全基因组核内染色体定位和相对于多种核结构的核区室化,这对于调节基因组功能至关重要。作为原理验证,我们使用 SPIN 将核区室映射(TSA-seq 和 DamID)和染色质相互作用数据(Hi-C)整合来自 K562 细胞的信息,以鉴定相对于核斑点、核纤层和与核仁可能相关的全基因组的 10 种空间区室化状态。这些 SPIN 状态显示了基因组空间组织的新的模式及其与其他 3D 基因组特征和基因组功能(转录和复制时间)的关系。SPIN 为核空间和功能区室化提供了重要的见解。