Sosa-Madrid Bolívar Samuel, Maniatis Gerasimos, Ibáñez-Escriche Noelia, Avendaño Santiago, Kranis Andreas
The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush Campus, Midlothian EH25 9RG, UK.
Institute for Animal Science and Technology, Universitat Politècnica de València, P.O. Box 2201, 46071 Valencia, Spain.
Animals (Basel). 2023 Oct 24;13(21):3306. doi: 10.3390/ani13213306.
Monitoring the genetic variance of traits is a key priority to ensure the sustainability of breeding programmes in populations under directional selection, since directional selection can decrease genetic variation over time. Studies monitoring changes in genetic variation have typically used long-term data from small experimental populations selected for a handful of traits. Here, we used a large dataset from a commercial breeding line spread over a period of twenty-three years. A total of 2,059,869 records and 2,062,112 animals in the pedigree were used for the estimations of variance components for the traits: body weight (BWT; 2,059,869 records) and hen-housed egg production (HHP; 45,939 records). Data were analysed with three estimation approaches: sliding overlapping windows, under frequentist (restricted maximum likelihood (REML)) and Bayesian (Gibbs sampling) methods; expected variances using coefficients of the full relationship matrix; and a "double trait covariances" analysis by computing correlations and covariances between the same trait in two distinct consecutive windows. The genetic variance showed marginal fluctuations in its estimation over time. Whereas genetic, maternal permanent environmental, and residual variances were similar for BWT in both the REML and Gibbs methods, variance components when using the Gibbs method for HHP were smaller than the variances estimated when using REML. Large data amounts were needed to estimate variance components and detect their changes. For Gibbs (REML), the changes in genetic variance from 1999-2001 to 2020-2022 were 82.29 to 93.75 (82.84 to 93.68) for BWT and 76.68 to 95.67 (98.42 to 109.04) for HHP. Heritability presented a similar pattern as the genetic variance estimation, changing from 0.32 to 0.36 (0.32 to 0.36) for BWT and 0.16 to 0.15 (0.21 to 0.18) for HHP. On the whole, genetic parameters tended slightly to increase over time. The expected variance estimates were lower than the estimates when using overlapping windows. That indicates the low effect of the drift-selection process on the genetic variance, or likely, the presence of genetic variation sources compensating for the loss. Double trait covariance analysis confirmed the maintenance of variances over time, presenting genetic correlations >0.86 for BWT and >0.82 for HHP. Monitoring genetic variance in broiler breeding programmes is important to sustain genetic progress. Although the genetic variances of both traits fluctuated over time, in some windows, particularly between 2003 and 2020, increasing trends were observed, which warrants further research on the impact of other factors, such as novel mutations, operating on the dynamics of genetic variance.
监测性状的遗传方差是确保定向选择下种群育种计划可持续性的关键优先事项,因为定向选择会随着时间推移降低遗传变异。监测遗传变异变化的研究通常使用来自为少数性状选择的小型实验种群的长期数据。在此,我们使用了一个商业育种品系长达二十三年的大型数据集。总共2,059,869条记录和系谱中的2,062,112只动物用于估计体重(BWT;2,059,869条记录)和入舍母鸡产蛋量(HHP;45,939条记录)这两个性状的方差分量。数据采用三种估计方法进行分析:滑动重叠窗口法,采用频率学派(限制最大似然法(REML))和贝叶斯(吉布斯抽样)方法;使用完全关系矩阵系数的期望方差;以及通过计算两个不同连续窗口中同一性状之间的相关性和协方差进行“双性状协方差”分析。遗传方差估计值随时间呈现边际波动。虽然在REML和吉布斯方法中,BWT的遗传、母体永久环境和残差方差相似,但使用吉布斯方法时HHP的方差分量小于使用REML时估计的方差。估计方差分量并检测其变化需要大量数据。对于吉布斯(REML)方法,BWT从1999 - 2001年到2020 - 2022年遗传方差的变化为82.29至93.75(82.84至93.68),HHP为76.68至95.67(98.42至109.04)。遗传力呈现出与遗传方差估计相似的模式,BWT从0.32变为0.36(0.32至0.36),HHP从0.16变为0.15(0.21至0.18)。总体而言,遗传参数随时间略有增加趋势。期望方差估计值低于使用重叠窗口时的估计值。这表明漂变 - 选择过程对遗传方差的影响较小,或者可能存在补偿损失的遗传变异来源。双性状协方差分析证实了方差随时间的维持,BWT的遗传相关性>0.86,HHP>0.82。监测肉鸡育种计划中的遗传方差对于维持遗传进展很重要。尽管两个性状的遗传方差随时间波动,但在某些窗口,特别是2003年至2020年之间,观察到增加趋势,这需要进一步研究其他因素,如新突变,对遗传方差动态的影响。