Partitioning of genomic variance reveals biological pathways associated with udder health and milk production traits in dairy cattle

被引:25
|
作者
Edwards, Stefan M. [1 ]
Thomsen, Bo [2 ]
Madsen, Per [1 ]
Sorensen, Peter [1 ]
机构
[1] Aarhus Univ, Dept Mol Biol & Genet, Ctr Quantitat Genet & Genom, DK-8830 Tjele, Denmark
[2] Aarhus Univ, Dept Mol Biol & Genet, DK-8830 Tjele, Denmark
基金
欧盟第七框架计划;
关键词
HERITABILITY; NUCLEOTIDE; COMPONENTS; POWERFUL; RETINOL; MODELS; SETS; KEGG;
D O I
10.1186/s12711-015-0132-6
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Background: We have used a linear mixed model (LMM) approach to examine the joint contribution of genetic markers associated with a biological pathway. However, with these markers being scattered throughout the genome, we are faced with the challenge of modelling the contribution from several, sometimes even all, chromosomes at once. Due to linkage disequilibrium (LD), all markers may be assumed to account for some genomic variance; but the question is whether random sets of markers account for the same genomic variance as markers associated with a biological pathway? Results: We applied the LMM approach to identify biological pathways associated with udder health and milk production traits in dairy cattle. A random gene sampling procedure was applied to assess the biological pathways in a dataset that has an inherently complex genetic correlation pattern due to the population structure of dairy cattle, and to linkage disequilibrium within the bovine genome and within the genes associated to the biological pathway. Conclusions: Several biological pathways that were significantly associated with health and production traits were identified in dairy cattle; i.e. the markers linked to these pathways explained more of the genomic variance and provided a better model fit than 95% of the randomly sampled gene groups. Our results show that immune related pathways are associated with production traits, and that pathways that include a causal marker for production traits are identified with our procedure. We are confident that the LMM approach provides a general framework to exploit and integrate prior biological information and could potentially lead to improved understanding of the genetic architecture of complex traits and diseases.
引用
收藏
页数:13
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