Understanding Patterns of Life History Trait Covariation in an Untapped Resource, the Lab Mouse.

IF 1.8 3区 生物学 Q3 PHYSIOLOGY Physiological and Biochemical Zoology Pub Date : 2023-09-01 Epub Date: 2023-07-07 DOI:10.1086/725435
Chloe C Josefson, Wendy R Hood
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Abstract

AbstractThrough artificial selection and inbreeding, strains of laboratory mice have been developed that vary in the expression of a single or suite of desired traits valuable to biomedical research. In addition to the selected trait(s), these strains also display variation in pelage color, body size, physiology, and life history. This article exploits the broad phenotypic variation across lab mouse strains to evaluate the relationships between life history and metabolism. Life history variation tends to exist along a fast-slow continuum. There has been considerable interest in understanding the ecological and evolutionary factors underlying life history variation and the physiological and metabolic processes that support them. Yet it remains unclear how these key traits scale across hierarchical levels, as ambiguous empirical support has been garnered at the intraspecific level. Within-species investigations have been thwarted by methodological constraints and environmental factors that obscure the genetic architecture underlying the hypothesized functional integration of life history and metabolic traits. In this analysis, we used the publicly available Mouse Phenome Database by the Jackson Laboratory to investigate the relationships among life history traits (e.g., body size, reproduction, and life span) and metabolic traits (e.g., daily energy expenditure and insulin-like growth factor 1 concentration). Our findings revealed significant variation in reproductive characteristics across strains of mice as well as relationships among life history and metabolic traits. We found evidence of variation along the fast-slow life history continuum, though the direction of some relationships among these traits deviated from interspecific predictions laid out in previous literature. Furthermore, our results suggest that the strength of these relationships are strongest earlier in life.

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在一个未命名的资源,实验室老鼠中理解生活史特征的变异模式。
摘要通过人工选择和近亲繁殖,已经开发出对生物医学研究有价值的单一或一套所需性状表达不同的实验室小鼠品系。除了选定的性状外,这些菌株还表现出不同的毛皮颜色、体型、生理学和生活史。本文利用实验室小鼠品系之间广泛的表型变异来评估生活史和代谢之间的关系。生活史的变化往往沿着一个快-慢的连续体存在。人们对理解生命史变异背后的生态和进化因素以及支持它们的生理和代谢过程非常感兴趣。然而,由于在种内水平上获得了模糊的经验支持,目前尚不清楚这些关键特征是如何在等级水平上扩展的。种内研究受到方法限制和环境因素的阻碍,这些因素掩盖了假设的生活史和代谢特征功能整合的遗传结构。在这项分析中,我们使用杰克逊实验室公开的小鼠表型数据库来研究生活史特征(如体型、繁殖和寿命)与代谢特征(如每日能量消耗和胰岛素样生长因子1浓度)之间的关系。我们的研究结果揭示了不同品种小鼠生殖特征的显著差异,以及生活史和代谢特征之间的关系。我们发现了沿着快-慢生活史连续体变化的证据,尽管这些特征之间的一些关系的方向偏离了以前文献中提出的种间预测。此外,我们的研究结果表明,这些关系的强度在生命早期最强。
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来源期刊
CiteScore
3.20
自引率
6.20%
发文量
62
审稿时长
6-12 weeks
期刊介绍: Physiological and Biochemical Zoology: Ecological and Evolutionary Approaches primarily publishes original research in animal physiology and biochemistry as considered from behavioral, ecological, and/or evolutionary perspectives. Studies at all levels of biological organization from the molecular to the whole organism are welcome, and work that integrates across levels of organization is particularly encouraged. Studies that focus on behavior or morphology are welcome, so long as they include ties to physiology or biochemistry, in addition to having an ecological or evolutionary context. Subdisciplines of interest include nutrition and digestion, salt and water balance, epithelial and membrane transport, gas exchange and transport, acid-base balance, temperature adaptation, energetics, structure and function of macromolecules, chemical coordination and signal transduction, nitrogen metabolism and excretion, locomotion and muscle function, biomechanics, circulation, behavioral, comparative and mechanistic endocrinology, sensory physiology, neural coordination, and ecotoxicology ecoimmunology.
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