Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Apr 18:9:848027.
doi: 10.3389/fvets.2022.848027. eCollection 2022.

Identification of Key Pathways Associated With Residual Feed Intake of Beef Cattle Based on Whole Blood Transcriptome Data Analyzed Using Gene Set Enrichment Analysis

Affiliations

Identification of Key Pathways Associated With Residual Feed Intake of Beef Cattle Based on Whole Blood Transcriptome Data Analyzed Using Gene Set Enrichment Analysis

Godstime A Taiwo et al. Front Vet Sci. .

Abstract

We applied whole blood transcriptome analysis and gene set enrichment analysis to identify pathways associated with divergent selection for low or high RFI in beef cattle. A group of 56 crossbred beef steers (average BW = 261 ± 18.5 kg) were adapted to a high-forage total mixed ration in a confinement dry lot equipped with GrowSafe intake nodes for period of 49 d to determine their residual feed intake (RFI). After RFI determination, whole blood samples were collected from beef steers with the lowest RFI (most efficient; low-RFI; n = 8) and highest RFI (least efficient; high-RFI; n = 8). Prior to RNA extraction, whole blood samples collected were composited for each steer. Sequencing was performed on an Illumina NextSeq2000 equipped with a P3 flow. Gene set enrichment analysis (GSEA) was used to analyze differentially expressed gene sets and pathways between the two groups of steers. Results of GSEA revealed pathways associated with metabolism of proteins, cellular responses to external stimuli, stress, and heat stress were differentially inhibited (false discovery rate (FDR) < 0.05) in high-RFI compared to low-RFI beef cattle, while pathways associated with binding and uptake of ligands by scavenger receptors, scavenging of heme from plasma, and erythrocytes release/take up oxygen were differentially enriched (FDR < 0.05) in high-RFI, relative to low-RFI beef cattle. Taken together, our results revealed that beef steers divergently selected for low or high RFI revealed differential expressions of genes related to protein metabolism and stress responsiveness.

Keywords: cellular response; feed efficiency; heat stress; oxidative stress; protein metabolism.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Similar articles

Cited by

References

    1. Koch RM, Swiger LA, Chambers D, Gregory KE. Efficiency of food use in beef cattle. J Anim Sci. (1963) 22:486–94. 10.2527/jas1963.222486x - DOI
    1. Alexandre PA, Kogelman LJ, Santana MH, Passarelli D, Pulz LH, Fantinato-Neto P, et al. . Liver transcriptomic networks reveal main biological processes associated with feed efficiency in beef cattle. BMC Genomics. (2015) 16:s12864–015. 10.1186/s12864-015-2292-8 - DOI - PMC - PubMed
    1. Kong RS, Liang G, Chen Y, Stothard P, Guan I. Transcriptome profiling of the rumen epithelium of beef cattle differing in residual feed intake. BMC Genomics. (2016) 17:592. 10.1186/s12864-016-2935-4 - DOI - PMC - PubMed
    1. Mukiibi R, Vinsky M, Keogh KA, Fitzsimmons C, Stothard P, Waters SM, et al. . Transcriptome analyses reveal reduced hepatic lipid synthesis and accumulation in more feed efficient beef cattle. Sci Rep. (2018) 8:7303. 10.1038/s41598-018-25605-3 - DOI - PMC - PubMed
    1. MacNeil MD, Berry DP, Clark SA, Crowley JJ, Scholtz MM. Evaluation of partial body weight for predicting body weight and average daily gain in growing beef cattle. Transl Anim Sci. (2021) 5:1–12. 10.1093/tas/txab126 - DOI - PMC - PubMed