Identification and Functional Prediction of Long Non-Coding RNA in Longissimus Dorsi Muscle of Queshan Black and Large White Pigs

• Published in: Genes Vol. 14; no. 1; p. 197
• Main Authors: Dou, Yaqing, Qi, Kunlong, Liu, Yingke, Li, Chenlei, Song, Chenglei, Wei, Yilin, Zhang, Zhe, Li, Xinjian, Wang, Kejun, Li, Xiuling, Qiao, Ruimin, Yang, Feng, Han, Xuelei
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 12.01.2023; MDPI
• Subjects: Adipocytes; Animals; Genes; Genomes; Hogs; intramuscular fat; large white pigs; Lipid metabolism; Lipid Metabolism - genetics; Lipids; Lipogenesis; LncRNAs; MAP kinase; Meat quality; Metabolism; Muscle, Skeletal - metabolism; Non-coding RNA; Phosphorylation; Pork; pork quality; Quality control; queshan black pigs; RNA, Long Noncoding - genetics; RNA, Long Noncoding - metabolism; RNA, Messenger - genetics; RNA-Seq; Signal transduction; Software; Stat1 protein; Swine - genetics; United States > US; pork quality; intramuscular fat; large white pigs; LncRNAs; queshan black pigs
• ISSN: 2073-4425; 2073-4425
• DOI: 10.3390/genes14010197

Long non-coding RNA (lncRNA) participates in the regulation of various biological processes, but its function and characteristics in intramuscular fat (IMF) deposition in different breeds of pigs have not been fully understood. IMF content is one of the important factors affecting pork quality. In the present study, the differentially expressed lncRNAs (DE lncRNAs) and their target genes were screened by comparing Queshan Black (QS) and Large White (LW) pigs based on RNA-seq. The results displayed 55 DE lncRNAs between QS and LW, 29 upregulated and 26 downregulated, with 172 co-located target genes, and 6203 co-expressed target genes. The results of GO and KEGG analysis showed that the target genes of DE lncRNAs were involved in multiple pathways related to lipogenesis and lipid metabolism, such as the lipid biosynthetic process, protein phosphorylation, activation of MAPK activity, and the Jak-STAT signaling pathway. By constructing regulatory networks, lincRNA-ZFP42- , lincRNA-AMY2- , and/or lincRNA-AMY2/miR-204/ were sieved, and the results indicate that lncRNA could participate in IMF deposition through direct regulation or ceRNA. These findings provide a basis for analyzing the molecular mechanism of IMF deposition in pigs and lay a foundation for developing and utilizing high-quality resources of local pig breeds.