首页> 外文期刊>Evolution: International Journal of Organic Evolution >Antagonistic pleiotropy and mutation accumulation contribute to age-related decline in stress response
【24h】

Antagonistic pleiotropy and mutation accumulation contribute to age-related decline in stress response

机译:拮抗性的肺炎和突变积累有助于应激反应的年龄相关的下降

获取原文
获取原文并翻译 | 示例
       

摘要

As organisms age, the effectiveness of natural selection weakens, leading to age-related decline in fitness-related traits. The evolution of age-related changes associated with senescence is likely influenced by mutation accumulation (MA) and antagonistic pleiotropy (AP). MA predicts that age-related decline in fitness components is driven by age-specific sets of alleles, nonnegative genetic correlations within trait across age, and an increase in the coefficient of genetic variance. AP predicts that age-related decline in a trait is driven by alleles with positive effects on fitness in young individuals and negative effects in old individuals, and is expected to lead to negative genetic correlations within traits across age. We build on these predictions using an association mapping approach to investigate the change in additive effects of SNPs across age and among traits for multiple stress-response fitness-related traits, including cold stress with and without acclimation and starvation resistance. We found support for both MA and AP theories of aging in the age-related decline in stress tolerance. Our study demonstrates that the evolution of age-related decline in stress tolerance is driven by a combination of alleles that have age-specific additive effects, consistent with MA, as well as nonindependent and antagonistic genetic architectures characteristic of AP.
机译:作为生物年龄,自然选择的有效性削弱,导致健身相关性状的年龄相关的下降。与衰老相关的年龄相关变化的演变可能受到突变积累(MA)和拮抗性肺炎(AP)的影响。 MA预测健身组分的年龄相关的下降是由年龄特异性等位基因的驱动的,非年龄特征在特征中的非负遗传相关性,以及遗传方差系数的增加。 AP预测特征的年龄相关的下降是由对老年人的年轻人和负面影响的健身产生积极影响的等位基因驱动,并且预计将导致跨年龄的特征的负遗传相关性。我们使用关联映射方法构建这些预测,探讨了跨年龄和多种应激健身相关性状的SNP的添加剂效应的变化,包括具有和不加速和饥饿性的冷应激。我们发现对患者的衰老和AP理论的支持在应激耐受性的年龄相关的下降中。我们的研究表明,应激耐受性与年龄相关的减少的演变是由具有年龄特异性添加剂效应的等位基因的组合驱动,与MA的一致,以及AP的非依赖性和拮抗遗传架构。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号