Coordinated transcriptional and post-transcriptional epigenetic regulation during skeletal muscle development and growth in pigs

BackgroundN6-methyladenosine (m(6)A) and DNA 5-methylcytosine (5mC) methylation plays crucial roles in diverse biological processes, including skeletal muscle development and growth. Recent studies unveiled a potential link between these two systems, implicating the potential mechanism of coordinated transcriptional and post-transcriptional regulation in porcine prenatal myogenesis and postnatal skeletal muscle growth. MethodsImmunofluorescence and co-IP assays were carried out between the 5mC writers and m(6)A writers to investigate the molecular basis underneath. Large-scale in-house transcriptomic data were compiled for applying weighted correlation network analysis (WGCNA) to identify the co-expression patterns of m(6)A and 5mC regulators and their potential role in pig myogenesis. Whole-genome bisulfite sequencing (WGBS) and methylated RNA immunoprecipitation sequencing (MeRIP-seq) were performed on the skeletal muscle samples from Landrace pigs at four postnatal growth stages (days 30, 60, 120 and 180). ResultsSignificantly correlated expression between 5mC writers and m(6)A writers and co-occurrence of 5mC and m(6)A modification were revealed from public datasets of C2C12 myoblasts. The protein-protein interactions between the DNA methylase and the m(6)A methylase were observed in mouse myoblast cells. Further, by analyzing transcriptome data comprising 81 pig skeletal muscle samples across 27 developmental stages, we identified a 5mC/m(6)A epigenetic module eigengene and decoded its potential functions in pre- or post-transcriptional regulation in postnatal skeletal muscle development and growth of pigs. Following integrative multi-omics analyses on the WGBS methylome data and MeRIP-seq data for both m(6)A and gene expression profiles revealed a genome/transcriptome-wide correlated dynamics and co-occurrence of 5mC and m(6)A modifications as a consequence of 5mC/m(6)A crosstalk in the postnatal myogenesis progress of pigs. Last, we identified a group of myogenesis-related genes collaboratively regulated by both 5mC and m(6)A modifications in postnatal skeletal muscle growth in pigs. ConclusionsOur study discloses a potential epigenetic mechanism in skeletal muscle development and provides a novel direction for animal breeding and drug development of related human muscle-related diseases.

Automated summary

This study reveals the coordinated regulatory mechanism of 5mC and m(6)A in porcine prenatal myogenesis and postnatal skeletal muscle growth, and identifies a group of myogenesis-related genes collaboratively regulated by these two modifications.