Multiscale 3D genome reorganization during skeletal muscle stem cell lineage progression and aging.
Yu ZhaoYingzhe DingLiangqiang HeQin ZhouXiaona ChenYuying LiMaria Vittoria AlfonsiZhenguo WuHao SunHuating WangPublished in: Science advances (2023)
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.
Keyphrases
- transcription factor
- stem cells
- skeletal muscle
- gene expression
- genome wide
- single cell
- dna methylation
- dna binding
- insulin resistance
- induced apoptosis
- rna seq
- poor prognosis
- binding protein
- genome wide identification
- cell fate
- type diabetes
- long non coding rna
- metabolic syndrome
- signaling pathway
- adipose tissue
- mesenchymal stem cells
- cell death
- endoplasmic reticulum stress