期刊
BMC GENOMICS
卷 23, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s12864-022-08588-4
关键词
circRNA; Embryo; Skeletal muscle; Growth and development; ceRNA
资金
- New Agricultural Breeds Creation Project in Jiangsu Province [PZCZ201730]
- Fundamental Research Program of Shanxi Province [202103021223163]
- China Agriculture Research System [CARS-41]
- Priority Academic Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
In this study, chicken leg muscles at 14 and 20-day embryo ages were collected from fast- and slow-growing groups for RNA-seq analysis, identifying 245 and 440 differentially expressed circRNAs in the comparison groups F14vsF20 and S14vsS20, respectively. GO enrichment analysis revealed that the host genes of DE circRNAs were related to growth processes, such as transcription regulation, metabolic processes, and myofibril assembly. Further analysis identified key host genes and circRNA-miRNA pairs involved in skeletal muscle development in chickens.
Background Chicken provides humans with a large amount of animal protein every year, in which skeletal muscle plays a leading role. The embryonic skeletal muscle development determines the number of muscle fibers and will affect the muscle production of chickens. CircRNAs are involved in a variety of important biological processes, including muscle development. However, studies on circRNAs in the chicken embryo muscle development are still lacking. Results In the study, we collected chicken leg muscles at 14 and 20-day embryo ages both in the fast- and slow-growing groups for RNA-seq. We identified 245 and 440 differentially expressed (DE) circRNAs in the comparison group F14vsF20 and S14vsS20 respectively. GO enrichment analysis for the host genes of DE circRNAs showed that biological process (BP) terms in the top 20 related to growth in F14vsF20 were found such as positive regulation of transcription involved in G1/S phase of mitotic cell cycle, multicellular organismal macromolecule metabolic process, and multicellular organismal metabolic process. In group S14vsS20, we also found some BP terms associated with growth in the top 20 including actomyosin structure organization, actin cytoskeleton organization and myofibril assembly. A total of 7 significantly enriched pathways were obtained, containing Adherens junction and Tight junction. Further analysis of those pathways found three crucial host genes MYH9, YBX3, IGF1R in both fast- and slow-growing groups, three important host genes CTNNA3, AFDN and CREBBP only in the fast-growing group, and six host genes FGFR2, ACTN2, COL1A2, CDC42, DOCK1 and MYL3 only in the slow-growing group. In addition, circRNA-miRNA network also revealed some key regulation pairs such as novel_circ_0007646-miR-1625-5p, novel_circ_0007646-miR-1680-5p, novel_circ_0008913-miR-148b-5p, novel_circ_0008906-miR-148b-5p and novel_circ_0001640-miR-1759-3p. Conclusions Comprehensive analysis of circRNAs and their targets would contribute to a better understanding of the molecular mechanisms in poultry skeletal muscle and it also plays an important guiding role in the next research.
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