Multiscale 3D genome reorganization during skeletal muscle stem cell lineage progression and aging

染色质 增强子 生物 染色体构象捕获 转录因子 CTCF公司 基因组 谱系(遗传) 转录组 基因座(遗传学) 计算生物学 细胞生物学 基因 遗传学 基因表达
作者
Yu Zhao,Yingzhe Ding,Liangqiang He,Qin Zhou,Xiaona Chen,Yuying Li,Maria Vittoria Alfonsi,Zhenguo Wu,Hao Sun,Huating Wang
出处
期刊:Science Advances [American Association for the Advancement of Science]
卷期号:9 (7) 被引量:27
标识
DOI:10.1126/sciadv.abo1360
摘要

Little is known about three-dimensional (3D) genome organization in skeletal muscle stem cells [also called satellite cells (SCs)]. Here, we comprehensively map the 3D genome topology reorganization during mouse SC lineage progression. Specifically, rewiring at the compartment level is most pronounced when SCs become activated. Marked loss in topologically associating domain (TAD) border insulation and chromatin looping also occurs during early activation process. Meanwhile, TADs can form TAD clusters and super-enhancer-containing TAD clusters orchestrate stage-specific gene expression. Furthermore, we uncover that transcription factor PAX7 is pivotal in enhancer-promoter (E-P) loop formation. We also identify cis-regulatory elements that are crucial for local chromatin organization at Pax7 locus and Pax7 expression. Lastly, we unveil that geriatric SC displays a prominent gain in long-range contacts and loss of TAD border insulation. Together, our results uncover that 3D chromatin extensively reorganizes at multiple architectural levels and underpins the transcriptome remodeling during SC lineage development and SC aging.
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