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通过在遗传模型中纳入显性效应来改进绵羊数量性状的遗传评估。

Improvement in genetic evaluation of quantitative traits in sheep by enriching genetic model with dominance effects.

作者信息

Ghafouri-Kesbi Farhad, Mokhtari Morteza, Gholizadeh Mohsen

机构信息

Department of Animal Science, Faculty of Agriculture, Bu-Ali Sina University, Hamedan, Iran.

Department of Animal Science, Faculty of Agriculture, University of Jiroft, Jiroft, Iran.

出版信息

Sci Rep. 2025 Aug 17;15(1):30144. doi: 10.1038/s41598-025-16005-5.

DOI:10.1038/s41598-025-16005-5
PMID:40820152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12358534/
Abstract

Although dominance effects play a major role in quantitative genetics, most studies on quantitative traits have often neglected dominance effects, assuming alleles act additively. Therefore, the aim followed here was to quantify the proportion of variation in the early growth of Baluchi sheep that was attributed to dominance effects. Data collected over a 28-year period at the Baluchi sheep breeding station was used in this study. Traits evaluated were birth weight (BW), weaning weight (WW) and average daily gain (ADG). Each trait was analyzed with a series of twelve animal models which included different combinations of additive genetic, dominance genetic, maternal genetic and maternal permanent environmental effects. The Akaike's information criterion (AIC) was used to rank models. The predictive ability of models was measured using the mean squared error of prediction (MSE) and Pearson's correlation coefficient between the real and predicted values of records (r([Formula: see text],[Formula: see text])). Correlations between traits due to additive and dominance effects were estimated using bivariate analyses. For all traits studied, including dominance effects improved the likelihood of the fitting model. In addition, models that included dominance effects had the better predictive ability as provided higher r([Formula: see text],[Formula: see text]) and lower MSE. However, accounting for dominance effects significantly increased the computing burden evidenced by considerably longer computing time and a huge amount of memory required. By including dominance effects in the model, additive genetic variance did not change, but residual variance decreased significantly up to 41%, which indicated that the dominance component distangelled from residual variance. For BW, WW and ADG, dominance genetic variance was 6.61, 1.91, and 2.73 times greater than additive genetic variance and contributed 87%, 65% and 73% to the total genetic variance, respectively. Estimates of dominance heritability ([Formula: see text]), were 0.29 ± 0.06, 0.15 ± 0.07 and 0.20 ± 0.07 for BW, WW and ADG, respectively. Additive heritability ([Formula: see text]), was 0.05 ± 0.01 for BW, 0.08 ± 0.02 for WW and 0.07 ± 0.02 for ADG, respectively. By including dominance effects in the model, the accuracy of additive breeding values increased by 8%, 8% and 11% for BW, WW and ADG, respectively. Correlation between additive breeding values obtained from the best model and the best model without dominance effects were close to unity for all traits studied, indicating negligible changes in the additive breeding values and little chance for re-ranking of top animals across models. While additive genetic correlations were all positive and high, the dominance genetic correlation between WW and ADG was positively high (0.99), and between other pairs of traits was negative. Although the inclusion of dominance effects in the model did not change the ranking of top animals and had high computational requirements, it improved the predictive performance of the model and led to a significantly better data fit and an increase in the accuracy of additive breeding values. Therefore, including dominance effects in the model for genetic evaluation of the early growth of Baluchi lambs can be a reasonable recommendation.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/12358534/f3f0542e3357/41598_2025_16005_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/12358534/0358a9737b56/41598_2025_16005_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/12358534/f3f0542e3357/41598_2025_16005_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/12358534/0358a9737b56/41598_2025_16005_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/12358534/f3f0542e3357/41598_2025_16005_Fig2_HTML.jpg
摘要

尽管显性效应在数量遗传学中起着重要作用,但大多数关于数量性状的研究往往忽略了显性效应,假设等位基因具有加性作用。因此,本研究的目的是量化俾路支绵羊早期生长中归因于显性效应的变异比例。本研究使用了在俾路支绵羊育种站28年期间收集的数据。评估的性状包括出生体重(BW)、断奶体重(WW)和平均日增重(ADG)。每个性状都用一系列十二个动物模型进行分析,这些模型包括加性遗传、显性遗传、母体遗传和母体永久环境效应的不同组合。使用赤池信息准则(AIC)对模型进行排名。模型的预测能力通过预测均方误差(MSE)以及记录的实际值和预测值之间的皮尔逊相关系数(r([公式:见正文],[公式:见正文]))来衡量。使用双变量分析估计加性和显性效应导致的性状之间的相关性。对于所有研究的性状,包括显性效应提高了拟合模型的似然性。此外,包含显性效应的模型具有更好的预测能力,因为其r([公式:见正文],[公式:见正文])更高且MSE更低。然而,考虑显性效应显著增加了计算负担,表现为计算时间显著延长以及需要大量内存。通过在模型中包含显性效应,加性遗传方差没有变化,但残差方差显著降低了41%,这表明显性成分从残差方差中分离出来。对于BW、WW和ADG,显性遗传方差分别比加性遗传方差大6.61、1.91和2.73倍,分别占总遗传方差的87%、65%和73%。BW、WW和ADG的显性遗传力([公式:见正文])估计值分别为0.29±0.06、0.15±0.07和0.20±0.07。加性遗传力([公式:见正文]),BW为0.05±0.01,WW为0.08±0.02,ADG为0.07±0.02。通过在模型中包含显性效应,BW、WW和ADG的加性育种值准确性分别提高了8%、8%和11%。对于所有研究的性状,从最佳模型获得的加性育种值与不包含显性效应的最佳模型之间的相关性接近1,表明加性育种值变化可忽略不计,且跨模型对顶级动物重新排名的可能性很小。虽然加性遗传相关性均为正且较高,但WW和ADG之间的显性遗传相关性为正且较高(0.99),其他性状对之间为负。尽管在模型中包含显性效应没有改变顶级动物的排名且计算要求较高,但它提高了模型的预测性能,导致数据拟合显著更好且加性育种值准确性提高。因此,在俾路支羔羊早期生长的遗传评估模型中包含显性效应是一个合理的建议。

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