Literature DB >> 33311457

Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells.

Minchul Kim1, Vedran Franke2, Bettina Brandt1, Elijah D Lowenstein1, Verena Schöwel3, Simone Spuler3, Altuna Akalin4, Carmen Birchmeier5.   

Abstract

Syncytial skeletal muscle cells contain hundreds of nuclei in a shared cytoplasm. We investigated nuclear heterogeneity and transcriptional dynamics in the uninjured and regenerating muscle using single-nucleus RNA-sequencing (snRNAseq) of isolated nuclei from muscle fibers. This revealed distinct nuclear subtypes unrelated to fiber type diversity, previously unknown subtypes as well as the expected ones at the neuromuscular and myotendinous junctions. In fibers of the Mdx dystrophy mouse model, distinct subtypes emerged, among them nuclei expressing a repair signature that were also abundant in the muscle of dystrophy patients, and a nuclear population associated with necrotic fibers. Finally, modifications of our approach revealed the compartmentalization in the rare and specialized muscle spindle. Our data identifies nuclear compartments of the myofiber and defines a molecular roadmap for their functional analyses; the data can be freely explored on the MyoExplorer server ( https://shiny.mdc-berlin.de/MyoExplorer/ ).

Entities:  

Year:  2020        PMID: 33311457     DOI: 10.1038/s41467-020-20064-9

Source DB:  PubMed          Journal:  Nat Commun        ISSN: 2041-1723            Impact factor:   14.919


  64 in total

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  23 in total

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