Genomic regions underlying uniformity of yearling weight in Nellore cattle evaluated under different response variables

被引:12
|
作者
de Souza Iung, Laiza Helena [1 ]
Mulder, Herman Arend [2 ]
de Rezende Neves, Haroldo Henrique [3 ]
Carvalheiro, Roberto [1 ]
机构
[1] Sao Paulo State Univ Unesp, Sch Agr & Vet Sci, FCAV UNESP, Via Acesso Prof Paulo Donato Castelane S-N, BR-14884900 Sao Paulo, Brazil
[2] Wageningen Univ & Res Anim Breeding & Genom, POB 338, NL-6700 AH Wageningen, Netherlands
[3] GenSys Consultores Associados SS Ltda, BR-90680000 Porto Alegre, RS, Brazil
来源
BMC GENOMICS | 2018年 / 19卷
关键词
Beef cattle; DHGLM; Genetic heterogeneity of residual variance; Growth traits; GWAS; Micro-environmental sensitivity; QUANTITATIVE TRAIT LOCI; SINGLE NUCLEOTIDE POLYMORPHISMS; LIPOPROTEIN-LIPASE GENE; HEAT-STRESS; CARCASS COMPOSITION; RESIDUAL VARIANCE; FAT DEPOSITION; FEED-INTAKE; LPL GENE; T-CELL;
D O I
10.1186/s12864-018-5003-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: In livestock, residual variance has been studied because of the interest to improve uniformity of production. Several studies have provided evidence that residual variance is partially under genetic control; however, few investigations have elucidated genes that control it. The aim of this study was to identify genomic regions associated with within-family residual variance of yearling weight (YW; N = 423) in Nellore bulls with high density SNP data, using different response variables. For this, solutions from double hierarchical generalized linear models (DHGLM) were used to provide the response variables, as follows: a DGHLM assuming non-null genetic correlation between mean and residual variance (r(mv) not equal 0) to obtain deregressed EBV for mean (dEBV(m)) and residual variance (dEBV(v)); and a DHGLM assuming r(mv) = 0 to obtain two alternative response variables for residual variance, dEBV(v)_(r0) and log-transformed variance of estimated residuals (ln_sigma(2)((e) over cap)). Results: The dEBV(m) and dEBV(v) were highly correlated, resulting in common regions associated with mean and residual variance of YW. However, higher effects on variance than the mean showed that these regions had effects on the variance beyond scale effects. More independent association results between mean and residual variance were obtained when null rmv was assumed. While 13 and 4 single nucleotide polymorphisms (SNPs) showed a strong association (Bayes Factor > 20) with dEBV(v) and ln_ sigma(2)((e) over cap), respectively, only suggestive signals were found for dEBV(v)_(r0). All overlapping 1-Mb windows among top 20 between dEBV(m) and dEBV(v) were previously associated with growth traits. The potential candidate genes for uniformity are involved in metabolism, stress, inflammatory and immune responses, mineralization, neuronal activity and bone formation. Conclusions: It is necessary to use a strategy like assuming null r(mv) to obtain genomic regions associated with uniformity that are not associated with the mean. Genes involved not only in metabolism, but also stress, inflammatory and immune responses, mineralization, neuronal activity and bone formation were the most promising biological candidates for uniformity of YW. Although no clear evidence of using a specific response variable was found, we recommend consider different response variables to study uniformity to increase evidence on candidate regions and biological mechanisms behind it.
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页数:13
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