Transcriptome profiling of muscle in Nelore cattle phenotypically divergent for the ribeye muscle area
This study aimed to use RNA-Seq to identify differentially expressed genes (DEGs) in muscle of uncastrated Nelore males phenotypically divergent for ribeye muscle area (REA). A total of 80 animals were phenotyped for REA, and 15 animals each with the highest REA and the lowest REA were selected for...
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Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 2020-03, Vol.112 (2), p.1257-1263 |
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Zusammenfassung: | This study aimed to use RNA-Seq to identify differentially expressed genes (DEGs) in muscle of uncastrated Nelore males phenotypically divergent for ribeye muscle area (REA). A total of 80 animals were phenotyped for REA, and 15 animals each with the highest REA and the lowest REA were selected for analyses. DEGs found (N = 288) belonging to families related to muscle cell growth, development, motility and proteolysis, such as actin, myosin, collagen, integrin, solute carrier, ubiquitin and kelch-like. Functional analysis showed that many of the significantly enriched gene ontology terms were closely associated with muscle development, growth, and degradation. Through co-expression network analysis, we predicted three hub genes (PPP3R1, FAM129B and UBE2G1), these genes are involved in muscle growth, proteolysis and immune system. The genes expression levels and its biological process found this study may result in differences in muscle deposition, and therefore, Nelore animals with different REA proportions.
•The differences in gene expression highlight the complexity of the longissumis thoracis transcriptome in Nelore cattle.•Differentially expressed genes found play a role in muscle growth, development, and degradation.•We predicted three hub genes (PPP3R1, FAM129B and UBE2G1).•Hub genes are involved in muscle growth, proteolysis and immune system.•Hub genes found may have a putative effect on development and growth muscle of the Nelore cattle. |
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ISSN: | 0888-7543 1089-8646 |
DOI: | 10.1016/j.ygeno.2019.07.012 |