四种啮齿类动物骨盆的比较数量遗传学及遗传协方差和相关结构的保存

IF 1.9 2区 生物学 Q3 EVOLUTIONARY BIOLOGY Evolutionary Biology Pub Date : 2022-02-21 DOI:10.1007/s11692-022-09559-z
Carl J. Saltzberg, Laura I. Walker, Lee E. Chipps-Walton, Bárbara M. A. Costa, Ángel E. Spotorno, Scott J. Steppan
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引用次数: 3

摘要

数量遗传学是在微观进化尺度上预测表型进化的有力工具。这种预测能力主要来自朗德方程(Δz′s = Gβ),这是育种方程的多变量扩展,其中表型变化(Δz′s)是通过遗传协方差(G)和选择(β)来预测的。进化生物学家提出,如果预测扩展到更长的时间尺度,数量遗传学可以在微观和宏观进化模式之间建立桥梁。虽然在数学上是可能的,但对跨代或跨物种进行定量遗传预测仍存在争议,主要是在假设g矩阵长期稳定的情况下。在这里,我们通过对南美叶耳鼠Phyllotis vaccum和P. darwini进行全同胞和半同胞繁殖计划,测试了在宏观进化时间尺度上的稳定性,并估计了8种骨盆特征的g矩阵。为了扩大我们的系统发育广度,我们结合了两个额外的g矩阵,测量来自Kohn &阿奇利1988年对老鼠啮齿类动物小家鼠和褐家鼠的研究。利用系统发育比较框架和矩阵差异或相似性的四个独立度量,我们发现物种g -矩阵的进化差异与时间之间没有显著关联,这支持了至少某些结构的稳定性假设。然而,系统发育样本量必然很小。我们认为协方差结构的微小波动可以迅速发生,但潜在的发育调节阻止了宏观进化尺度上的显著差异,类似于Ornstein-Uhlenbeck模式。需要扩大分类学抽样来检验这一建议。
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Comparative Quantitative Genetics of the Pelvis in Four-Species of Rodents and the Conservation of Genetic Covariance and Correlation Structure

Quantitative genetics is a powerful tool for predicting phenotypic evolution on a microevolutionary scale. This predictive power primarily comes from the Lande equation (Δ = ), a multivariate expansion of the breeder’s equation, where phenotypic change (Δ) is predicted from the genetic covariances (G) and selection (β). Typically restricted to generational change, evolutionary biologists have proposed that quantitative genetics could bridge micro- and macroevolutionary patterns if predictions were expanded to longer timescales. While mathematically possible, making quantitative genetic predictions across generations or species is contentiously debated, principally in assuming long-term stability of the G-matrix. Here we tested stability at a macroevolutionary timescale by conducting full- and half-sib breeding programs in two species of sigmodontine rodents from South America, the leaf-eared mice Phyllotis vaccarum and P. darwini and estimated the G-matrices for eight pelvic traits. To expand our phylogenetic breadth, we incorporated two additional G-matrices measured for the same traits from Kohn & Atchley’s 1988 study of the murine rodents Mus musculus and Rattus norvegicus. Using a phylogenetic comparative framework and four separate metrics of matrix divergence or similarity, we found no significant association between evolutionary divergence among species G-matrices and time, supporting the assumption of stability for at least some structures. However, the phylogenetic sample size is necessarily small. We suggest that small fluctuations in covariance structure can occur rapidly, but underlying developmental regulation prevents significant divergence at macroevolutionary scales, analogous to an Ornstein–Uhlenbeck pattern. Expanded taxonomic sampling will be needed to test this suggestion.

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来源期刊
Evolutionary Biology
Evolutionary Biology 生物-进化生物学
CiteScore
3.80
自引率
4.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: The aim, scope, and format of Evolutionary Biology will be based on the following principles: Evolutionary Biology will publish original articles and reviews that address issues and subjects of core concern in evolutionary biology. All papers must make original contributions to our understanding of the evolutionary process. The journal will remain true to the original intent of the original series to provide a place for broad syntheses in evolutionary biology. Articles will contribute to this goal by defining the direction of current and future research and by building conceptual links between disciplines. In articles presenting an empirical analysis, the results of these analyses must be integrated within a broader evolutionary framework. Authors are encouraged to submit papers presenting novel conceptual frameworks or major challenges to accepted ideas. While brevity is encouraged, there is no formal restriction on length for major articles. The journal aims to keep the time between original submission and appearance online to within four months and will encourage authors to revise rapidly once a paper has been submitted and deemed acceptable.
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