{"title":"Single-Step Genomic Reaction Norm and ssGWAS Reveal Heat-Load-Dependent Genetic Architecture of Age at Puberty in Yorkshire Gilts.","authors":"Chong Zhang, Jinglei Si, Xiaoxiao Song, Youen Xiao, Wenzhou Wang, Borong Liang, Shaoyun Li, Peiqing Cong, Yaosheng Chen, Xiaohong Liu","doi":"10.3390/ani16193085","DOIUrl":null,"url":null,"abstract":"<p><p>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 (<i>p</i> < 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.</p>","PeriodicalId":7955,"journal":{"name":"Animals","volume":"16 19","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13663369/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animals","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.3390/ani16193085","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0
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.
AnimalsAgricultural 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).