Transcriptome Profiling of the Liver in Nellore Cattle Phenotypically Divergent for RFI in Two Genetic Groups

• Published in: Animals (Basel) 2023-01, Vol.13 (3), p.359
• Main Authors: Serna-García, Marta, Fonseca, Larissa Fernanda Simielli, Panadero Romero, Joaquin Javier, Carretero Asuncion, Julian, Dos Santos Silva, Danielly Beraldo, Salatta, Bruna Maria, Frezarim, Gabriela Bonfá, Mercadante, Maria Eugênia Zerlotti, Bonilha, Sarah Figueiredo Martins, Ferro, Jesus Aparecido, De Albuquerque, Lucia Galvão
• Format: Article
• Language: English
• Subjects: Animal growth; Animal husbandry; Animal tissues; Animals; Beef cattle; Biological activity; Biological effects; Biomarkers; bovine; Cattle; Cell death; Corn; Cytotoxicity; Divergence; Efficiency; Energy metabolism; Farms; feed efficiency; Feeds; Gene expression; Genes; Homeostasis; Immune response; Immune system; Lipid metabolism; Lipids; Liver; liver tissue; Material requirements planning; Meat; Meat production; Metabolic pathways; miRNA; Mitochondria; Non-coding RNA; non-coding RNAs; Oxidative stress; Production costs; Protein turnover; Proteins; Ribonuclease MRP; RNA-Seq; Sustainable development; Transcriptomes; β2 Microglobulin
• ISSN: 2076-2615; 2076-2615
• DOI: 10.3390/ani13030359

The identification and selection of genetically superior animals for residual feed intake (RFI) could enhance productivity and minimize environmental impacts. The aim of this study was to use RNA-seq data to identify the differentially expressed genes (DEGs), known non-coding RNAs (ncRNAs), specific biomarkers and enriched biological processes associated with RFI of the liver in Nellore cattle in two genetic groups. In genetic group 1 (G1), 24 extreme RFI animals (12 low RFI (LRFI) versus 12 high RFI (HRFI)) were selected from a population of 60 Nellore bulls. The RNA-seq of the samples from their liver tissues was performed using an Illumina HiSeq 2000. In genetic group 2 (G2), 20 samples of liver tissue of Nellore bulls divergent for RFI (LRFI, = 10 versus HRFI, = 10) were selected from 83 animals. The raw data of the G2 were chosen from the ENA repository. A total of 1811 DEGs were found for the G1 and 2054 for the G2 ( -value ≤ 0.05). We detected 88 common genes in both genetic groups, of which 33 were involved in the immune response and in blocking oxidative stress. In addition, seven ( , , , , , , and ) possible gene biomarkers were identified through a receiver operating characteristic analysis (ROC) considering an AUC > 0.70. The gene was overexpressed in the LRFI group. This gene regulates the lipid metabolism protein turnover and inhibits cell death. We also found non-coding RNAs in both groups. MIR25 was up-regulated and SNORD16 was down-regulated in the LRFI for G1. For G2, up-regulated RNase_MRP and SCARNA10 were found. We highlight MIR25 as being able to act by blocking cytotoxicity and oxidative stress and RMRP as a blocker of mitochondrial damage. The biological pathways associated with RFI of the liver in Nellore cattle in the two genetic groups were for energy metabolism, protein turnover, redox homeostasis and the immune response. The common transcripts, biomarkers and metabolic pathways found in the two genetic groups make this unprecedented work even more relevant, since the results are valid for different herds raised in different ways. The results reinforce the biological importance of these known processes but also reveal new insights into the complexity of the liver tissue transcriptome of Nellore cattle.