Assessment and the regulation of adaptive phenotypic plasticity.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-10-15 Epub Date: 2024-10-17 DOI:10.1242/dev.203101
Karl A P Hill, Karin S Pfennig, David W Pfennig
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Abstract

Organisms can react to environmental variation by altering their phenotype, and such phenotypic plasticity is often adaptive. This plasticity contributes to the diversity of phenotypes across the tree of life. Generally, the production of these phenotypes must be preceded by assessment, where the individual acquires information about its environment and phenotype relative to that environment, and then determines if and how to respond with an alternative phenotype. The role of assessment in adaptive plasticity is, therefore, crucial. In this Review, we (1) highlight the need for explicitly considering the role of assessment in plasticity; (2) present two different models for how assessment and the facultative production of phenotypes are related; and (3) describe an overarching framework for how assessment evolves. In doing so, we articulate avenues of future work and suggest that explicitly considering the role of assessment in the evolution of plasticity is key to explaining how and when plasticity occurs. Moreover, we emphasize the need to understand the role of assessment in adaptive versus maladaptive plasticity, which is an issue that will become increasingly important in a rapidly changing world.

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适应性表型可塑性的评估和调节。
生物可通过改变其表型对环境变化做出反应,这种表型可塑性通常具有适应性。这种可塑性造就了生命之树上表型的多样性。一般来说,在产生这些表型之前必须先进行评估,即个体获取有关其所处环境和表型的信息,然后决定是否以及如何以另一种表型做出反应。因此,评估在适应性可塑性中的作用至关重要。在这篇综述中,我们将:(1)强调明确考虑评估在可塑性中的作用的必要性;(2)介绍两种不同的模型,说明评估与表型的面性产生之间的关系;(3)描述评估如何演化的总体框架。在此过程中,我们阐明了未来的工作方向,并提出明确考虑评估在可塑性进化过程中的作用是解释可塑性如何以及何时发生的关键。此外,我们强调有必要了解评估在适应性可塑性与适应性不良可塑性中的作用,这个问题在瞬息万变的世界中将变得越来越重要。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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David Ish-Horowicz FRS (1948-2024): outstanding scientific discovery, with a unique touch of selfless humanity. In preprints: early cell differentiation and mechanical environment. Transitions in development - an interview with Dorit Hockman. Emerin preserves stem cell survival through maintenance of centrosome and nuclear lamina structure. RAB6 GTPase is required for stem cell maintenance and cell migration in the gut epithelium.
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