Gene expression analysis of blood, liver, and muscle in cattle divergently selected for high and low residual feed intake

被引:30
|
作者
Khansefid, M. [1 ,2 ]
Millen, C. A. [2 ,3 ]
Chen, Y. [4 ]
Pryce, J. E. [1 ,5 ]
Chamberlain, A. J. [1 ]
Vander Jagt, C. J. [1 ]
Gondro, C. [6 ]
Goddard, M. E. [1 ,2 ]
机构
[1] Agr Victoria, Ctr AgriBiosci, AgriBio, Bundoora, Vic 3083, Australia
[2] Univ Melbourne, Fac Vet & Agr Sci, Dept Agr & Food Syst, Parkville, Vic 3010, Australia
[3] Univ New England, Agr Business Res Inst, Armidale, NSW 2351, Australia
[4] NSW Dept Primary Ind, Elizabeth Macarthur Agr Inst, Woodbridge Rd, Menangle, NSW 2568, Australia
[5] La Trobe Univ, Sch Appl Syst Biol, Bundoora, Vic 3086, Australia
[6] Univ New England, Sch Environm & Rural Sci, Armidale, NSW 2351, Australia
关键词
Bos taurus; differential gene expression; feed efficiency; residual feed intake; RNA sequencing; GENOMIC BREEDING VALUES; COMPLEX TRAITS; NELORE STEERS; DAIRY; EFFICIENCY;
D O I
10.2527/jas2016.1320
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Improving feed efficiency in cattle is important because it increases profitability by reducing costs, and it also shrinks the environmental footprint of cattle production by decreasing manure and greenhouse gas emissions. Residual feed intake (RFI) is 1 measurement of feed efficiency and is the difference between actual and predicted feed intake. Residual feed intake is a complex trait with moderate heritability, but the genes and biological processes associated with its variation still need to be found. We explored the variation in expression of genes using RNA sequencing to find genes whose expression was associated with RFI and then investigated the pathways that are enriched for these genes. In this study, we used samples from growing Angus bulls (muscle and liver tissues) and lactating Holstein cows (liver tissue and white blood cells) divergently selected for low and high RFI. Within each breed-tissue combination, the correlation between the expression of genes and RFI phenotypes, as well as GEBV, was calculated to determine the genes whose expression was correlated with RFI. There were 16,039 genes expressed in more than 25% of samples in 1 or more tissues. The expression of 6,143 genes was significantly associated with RFI phenotypes, and expression of 2,343 genes was significantly associated with GEBV for RFI (P < 0.05) in at least 1 tissue. The genes whose expression was correlated with RFI phenotype (or GEBV) within each breed-tissue combination were enriched for 158 (78) biological processes (Fisher Exact Statistics for gene-enrichment analysis, EASE score < 0.1) and associated with 13 (13) Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways (P < 0.05 and fold enrichment > 2). These biological processes were related to regulation of transcription, translation, energy generation, cell cycling, apoptosis, and proteolysis. However, the direction of the correlation between RFI and gene expression in some cases reversed between tissues. For instance, low levels of proteolysis in muscle were associated with high efficiency in growing bulls, but high levels of proteolysis in white blood cells were associated with efficiency of milk production in lactating cows.
引用
收藏
页码:4764 / 4775
页数:12
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