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Construction of circRNA-related ceRNA networks in longissimus dorsi muscle of Queshan Black and Large White pigs

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Abstract

Circular RNA (circRNA) is a class of non-coding RNA (ncRNA) that plays an important regulatory role in various biological processes of the organisms and has a major function in muscle growth and development. However, its molecular mechanisms of how it regulates pork quality remain unclear at present. In this study, we compared the longissimus dorsi (LD) muscle expression profiles of Queshan Black (QS) and Large White (LW) pigs to explore the role of circRNAs in meat quality using transcriptome sequencing. A total of 62 differentially expressed circRNAs (DECs), including 46 up- and 16 down-regulated, 39 differentially expressed miRNAs (DEmiRNAs), including 21 up- and 18 down-regulated and 404 differentially expressed mRNAs (DEMs), including 174 up- and 230 down-regulated were identified, and most circRNAs were composed of exons. Our results indicated that the DEC parent genes and DEMs were enriched in the positive regulation of fast-twitch skeletal muscle fiber contraction, relaxation of skeletal muscle, regulation of myoblast proliferation, AMPK signaling pathway, Wnt and Jak-STAT signaling pathway. Furthermore, circSETBP1/ssc-miR-149/PIK3CD and circGUCY2C/ssc-miR-425-3p/CFL1 were selected by constructing the competitive endogenous RNA (ceRNA) regulatory network, circSETBP1, circGUCY2C, PIK3CD and CFL1 had low expression level in QS, while ssc-miR-149 and ssc-miR-425-3p had higher expression level than LW, our analysis revealed that circSETBP1, circGUCY2C, ssc-miR-149, ssc-miR-425-3p, PIK3CD and CFL1 were associated with lipid regulation, cell proliferation and differentiation, so the two ceRNAs regulatory networks may play an important role in regulating intramuscular fat (IMF) deposition, thereby affecting pork quality. In conclusion, we described the gene regulation by the circRNA–miRNA–mRNA ceRNA networks by comparing QS and LW pigs LD muscle transcriptome, and the two new circRNA-associated ceRNA regulatory networks that could help to elucidate the formation mechanism of pork quality. The results provide a theoretical basis for further understanding the genetic mechanism of meat quality formation.

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Fig. 1

source statistics and d density distribution on the chromosomes of circRNAs

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Acknowledgements

This work was supported by Henan Key Research & Development Program (192102110067 and 202102110242), Pig Industry Technology System Innovation Team Project of Henan Province (S2012-06-G03), Grand Science and Technology Special Project in Tibet (212102110003), and the National Natural Science Foundation of China (32002142).

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Author contributions XH proposed conceptualization, methodology, wrote reviews and editing, administrated project; KQ performed verification and visualization, wrote original draft preparation; XH, YL and CL investigated; XH, XL and XL provided resources; KW and RQ performed supervision. All authors have read and agreed to the published version of the manuscript.

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Correspondence to Xuelei Han.

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The authors declare that they have no conflicts of interest.

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All of the experiments involving animals were carried out in accordance with the guidelines for the care and use of experimental animals established by the Ministry of Science and Technology of the People’s Republic of China (Approval Number 2006–398).

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Communicated by Joan Cerdá.

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Qi, K., Liu, Y., Li, C. et al. Construction of circRNA-related ceRNA networks in longissimus dorsi muscle of Queshan Black and Large White pigs. Mol Genet Genomics 297, 101–112 (2022). https://doi.org/10.1007/s00438-021-01836-4

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  • DOI: https://doi.org/10.1007/s00438-021-01836-4

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