健康苗猪毛发应激激素水平的遗传分析及其与回试反应的关系。

IF 5.1 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-08-06 DOI:10.1093/genetics/iyaf092
Fazhir Kayondo, Hayder Al-Shanoon, Yolande M Seddon, Dylan Carette, Carmen Cole, David M Janz, Frederic Fortin, John C S Harding, Michael K Dyck, Graham S Plastow, PigGen Canada, Jack C M Dekkers
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引用次数: 0

摘要

本研究探索了863头临床健康的约克郡×长白猪毛发中应激激素(皮质醇、可可松、脱氢表雄酮和脱氢表雄酮- s)水平的遗传学,并通过估计在27日龄进行的30秒回测反应的遗传相关性,评估了它们作为先天应激反应生物标志物的潜力。回测反应包括发声(VN, VI)和挣扎(SN, SI)的次数和强度。使用50K单核苷酸多态性(SNP)小组对猪进行基因分型,并将其归为650K个SNP,皮质醇、可可松、DHEA和DHEA- s水平的遗传力估计分别为0.33、0.04、0和0.31,而回测反应的遗传力估计范围为0.26至0.57。凋落物效应占应激激素水平表型变异的9%至16%,而回测反应没有。应激激素水平之间的遗传相关性在皮质醇和可的松之间最强(0.99±0.12),而回测反应之间的遗传相关性在0.60至0.99之间。皮质醇与VN(0.24±0.19)和VI(0.50±0.24)有中度遗传相关性,但与SN和SI无遗传相关性。全基因组关联研究确定了糖皮质激素受体基因(NR3C1)附近毛发皮质醇水平的主要数量性状位点(QTL),该基因解释了45.3%的遗传变异,这可能与之前在猪血液中该基因中发现的导致皮质醇水平的致病突变不同。该QTL rs341258564的主SNP位点多了一个小等位基因拷贝(频率=9%),使皮质醇水平降低30±6%,可的松水平降低17±4%,使VN增加5±2%。DHEA-S、皮质醇/DHEA-S、可的松/DHEA-S、VI和VN的QTL效应较小(占遗传变异的1.0 - 11.1%)。基于遗传变异解释的0.25 Mb窗口的排序基因集富集分析表明,与糖皮质激素水平相关的窗口在与能量产生和炎症抑制相关的生物学术语中富集。相反,与DHEA-S相关的细胞在与免疫激活、基因转录和转录后调控相关的生物过程中富集。这些发现建立了幼猪和临床健康猪应激反应的遗传基础,确定了毛发皮质醇水平的主要QTL的基因组位置,并表明幼猪和健康猪毛发中的皮质醇水平是猪对非传染性应激源的先天应对反应方式的潜在遗传生物标志物。这些结果为选择能够更好地应对非传染性压力源的猪开辟了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic analysis of stress hormone levels in hair of healthy nursery pigs and their relationships with backtest responses.

This study explored the genetics of the levels of stress hormones (cortisol, cortisone, DHEA, and DHEA-S) in hair of 863 clinically healthy Yorkshire × Landrace male pigs at ∼40 days of age and evaluated their potential as biomarkers of innate stress response by estimating genetic correlations with responses to a 30 s backtest performed at ∼27 days of age. Backtest responses included the number and intensity of vocalizations (VN and VI) and struggles (SN and SI). With pigs genotyped using a 50 K single nucleotide polymorphism (SNP) panel that was imputed to 650 K SNPs, heritability estimates for the levels of cortisol, cortisone, DHEA, and DHEA-S were 0.33, 0.04, 0, and 0.31, respectively, while those for backtest responses ranged from 0.26 to 0.57. Litter effects accounted for 9 to 16% of the phenotypic variance for stress hormone levels and none for backtest responses. Genetic correlation estimates among stress hormone levels were strongest between cortisol and cortisone (0.99 ± 0.12), while those among backtest responses ranged from 0.60 to 0.99. Cortisol was estimated to have moderate genetic correlations with VN (0.24 ± 0.19) and VI (0.50 ± 0.24) but not with SN and SI. Genome-wide association studies identified a major quantitative trait locus (QTL) for hair cortisol levels near the glucocorticoid receptor gene (NR3C1) that explained 45.3% of the genetic variance and that may be different than a causative mutation that was previously identified in this gene for cortisol levels in porcine blood. An extra copy of the minor allele (frequency = 9%) at the lead SNP for this QTL, rs341258564 originated from both parental breeds and reduced levels of cortisol by 30 ± 6% and of cortisone by 17 ± 4%, and increased VN by 5 ± 2%. Additional QTL with smaller effects (1.0 to 11.1% of genetic variance) were identified for DHEA-S, cortisol/DHEA-S, cortisone/DHEA-S, VI, and VN. Ranked gene set enrichment analyses of 0.25 Mb windows based on genetic variance explained showed that windows associated with glucocorticoid levels were enriched for biological terms related to energy production and suppression of inflammation. In contrast, those associated with DHEA-S were enriched for biological processes related to immunity activation and gene transcriptional and post-transcriptional regulation. These findings establish the genetic basis of stress response in young and clinically healthy pigs, identify the genomic location of a major QTL for hair cortisol levels, and show that cortisol levels in hair of young and healthy pigs are potential genetic biomarkers for the innate coping response style of pigs to noninfectious stressors. These results open avenues that can facilitate selection of pigs that cope better with noninfectious stressors.

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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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