bioRxivDevelopmental BiologyPreprint
seRNA PAM-1 regulates skeletal muscle satellite cell activation and aging through trans regulation of Timp2 expression synergistically with Ddx5
Karl Kam Hei SoiD, Yile HuangiD, Suyang ZhangiD, Liangqiang HeiD, Yuying LiiD, Xiaona CheniD, Yu Fen ZhaoiD, Yingzhe Ding, Jiajian ZhouiD, Jie YuaniD, Mai Har ShamiD, Hao SuniD, Huating WangiD
Abstract
Muscle satellite cells (SCs) are responsible for muscle homeostasis and regeneration; and lncRNAs play important roles in regulating SC activities. Here in this study, we identify PAM-1 (Pax7 Associated Muscle lncRNA) that is induced in activated SCs to promote SC activation into myoblast cells upon injury. PAM-1 is generated from a myoblast specific super-enhancer (SE); as a seRNA it binds with a number of target genomic loci predominantly in trans. Further studies demonstrate that it interacts with Ddx5 to tether PAM-1 SE to it inter-chromosomal targets Timp2 and Vim to activate the gene expression. Lastly, we show that PAM-1 expression is increased in aging SCs, which leads to enhanced inter-chromosomal interaction and target genes up-regulation. Altogether, our findings identify PAM-1 as a previously unknown lncRNA that regulates both SC activation and aging through its trans gene regulatory activity.
- organism: mouse
- assay: long-read sequencing
- assay: DNA methylation
- research focus: gene regulatory network inference
- research focus: differential expression
- research focus: cell type annotation
- approach: statistical model
- approach: experimental assay
- Citations
- 0
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