Single-Step Genomic Reaction Norm and ssGWAS Reveal Heat-Load-Dependent Genetic Architecture of Age at Puberty in Yorkshire Gilts.

IF 3.2 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Animals Pub Date : 2026-09-30 DOI:10.3390/ani16193085
Chong Zhang, Jinglei Si, Xiaoxiao Song, Youen Xiao, Wenzhou Wang, Borong Liang, Shaoyun Li, Peiqing Cong, Yaosheng Chen, Xiaohong Liu
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Abstract

Heat stress adversely affects porcine reproduction, but genetic variation in the response of age at puberty (AP) to heat exposure remains poorly characterized in gilts. We analyzed 4438 AP records from Yorkshire gilts using adjusted meteorological data and compared three heat-exposure gradients across five prepubertal windows. Pedigree- and single-step genomic reaction-norm models were fitted, followed by single-step genome-wide association analyses of the intercept and slope. Among the 15 exposure scenarios, the best-fitting model used the proportion of sustained heat-stress days in the 14-day window before first observed estrus; a one-standard-deviation increase in this measure was associated with a 7.64-day increase in AP. Both reaction-norm models detected significant genetic variance for environmental sensitivity (p < 0.001). The genomic intercept-slope genetic correlation was -0.524, and genetic variances and correlations varied across the exposure gradient. GEBVs rankings at the 10th and 90th percentiles of the exposure gradient were negatively correlated (Spearman's ρ = -0.742), and the most favorable 10% of gilts did not overlap between these two exposure levels. Intercept and slope window contributions were strongly correlated (Spearman's ρ = 0.822), although component-specific regions were also detected. Functional annotation highlighted candidate genes and biological processes related to neuroendocrine regulation, ovarian development, mitochondrial and redox homeostasis, and cellular stress responses. These findings reveal genetically heterogeneous heat sensitivity in AP, supporting environment-specific genomic evaluation for reproductive robustness in gilts.

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单步基因组反应规范和ssGWAS揭示了约克郡后备母猪青春期年龄的热负荷依赖遗传结构。
热应激对猪的繁殖有不利影响,但在后备母猪中,青春期年龄(AP)对热暴露的反应的遗传变异仍不清楚。我们利用调整后的气象数据分析了来自约克郡母猪的4438份AP记录,并比较了五个青春期前窗口的三种热暴露梯度。拟合系谱和单步基因组反应规范模型,然后对截距和斜率进行单步全基因组关联分析。在15种暴露情景中,最佳拟合模型采用首次观察发情前14天窗口内持续热应激天数的比例;该测量的一个标准差增加与7.64天AP增加相关。两种反应规范模型都检测到环境敏感性的显着遗传变异(p < 0.001)。基因组截斜率遗传相关系数为-0.524,遗传方差和相关系数在暴露梯度上存在差异。gebv在暴露梯度第10和第90百分位的排名呈负相关(Spearman's ρ = -0.742),最有利的10%后备母猪在这两个暴露水平之间没有重叠。截距窗和斜率窗的贡献是强相关的(Spearman ρ = 0.822),尽管也检测到组分特定区域。功能注释突出了与神经内分泌调节、卵巢发育、线粒体和氧化还原稳态以及细胞应激反应相关的候选基因和生物过程。这些发现揭示了AP的遗传异质性热敏性,支持了后备母猪生殖稳健性的环境特异性基因组评估。
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来源期刊
Animals
Animals Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
4.90
自引率
16.70%
发文量
3015
审稿时长
20.52 days
期刊介绍: Animals (ISSN 2076-2615) is an international and interdisciplinary scholarly open access journal. It publishes original research articles, reviews, communications, and short notes that are relevant to any field of study that involves animals, including zoology, ethnozoology, animal science, animal ethics and animal welfare. However, preference will be given to those articles that provide an understanding of animals within a larger context (i.e., the animals'' interactions with the outside world, including humans). There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental details and/or method of study, must be provided for research articles. Articles submitted that involve subjecting animals to unnecessary pain or suffering will not be accepted, and all articles must be submitted with the necessary ethical approval (please refer to the Ethical Guidelines for more information).
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