RBFOX2-dependent alternative splicing of Numb regulates Notch signaling during muscle stem cell activation

Satellite cells (SCs) are somatic stem cells essential for skeletal muscle regeneration. Most SCs remain quiescent in resting muscle, but they rapidly activate in response to stimuli. Although post-transcriptional regulation has been implicated in SC functions, the role of alternative splicing (AS) during SC activation remains unclear. Using in vivo fixation to preserve quiescent SCs, we uncovered rapid and extensive AS changes upon activation, affecting genes involved in fundamental pathways. We identified RBFOX2 as a key AS regulator in SCs; its loss delayed both SC activation and muscle regeneration. Particularly, RBFOX2 promotes the inclusion of exon 6 in Numb, a Notch pathway regulator. This exon is required for SC activation, and its skipping delays activation while upregulating Notch signaling. Altogether, our study provides the AS landscape during SC activation and demonstrates that a single-gene splicing change can significantly influence SC activation and essential pathways such as Notch signaling.

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Publication Details

Journal
Stem Cell Reports
Published
2025-12-19
DOI
https://doi.org/10.1016/j.stemcr.2025.102745
Primary Topic
Muscle Physiology and Disorders
Type
article
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article

RBFOX2-dependent alternative splicing of Numb regulates Notch signaling during muscle stem cell activation

Tom H. Cheung, Lok Pui Ngan, Kangning Lin, A. Dong et al.
Stem Cell Reports
Muscle Physiology and Disorders
article

RBFOX2-dependent alternative splicing of Numb regulates Notch signaling during muscle stem cell activation

Tom H. Cheung, Lok Pui Ngan, Kangning Lin, A. Dong, Erin H.Y. Tse, Jing Liu, Indigo T.C. Chan, Yishu Yin
article en

Abstract

Satellite cells (SCs) are somatic stem cells essential for skeletal muscle regeneration. Most SCs remain quiescent in resting muscle, but they rapidly activate in response to stimuli. Although post-transcriptional regulation has been implicated in SC functions, the role of alternative splicing (AS) during SC activation remains unclear. Using in vivo fixation to preserve quiescent SCs, we uncovered rapid and extensive AS changes upon activation, affecting genes involved in fundamental pathways. We identified RBFOX2 as a key AS regulator in SCs; its loss delayed both SC activation and muscle regeneration. Particularly, RBFOX2 promotes the inclusion of exon 6 in Numb, a Notch pathway regulator. This exon is required for SC activation, and its skipping delays activation while upregulating Notch signaling. Altogether, our study provides the AS landscape during SC activation and demonstrates that a single-gene splicing change can significantly influence SC activation and essential pathways such as Notch signaling.

Stem Cell ReportsVol. 21(1)
HKUST Shenzhen Research Institute (CN), University of Hong Kong (HK)
Openalex Percentile: Top 63%
Muscle Physiology and Disorders
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