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Developmental bias as a cause and consequence of adaptive radiation and divergence.

作者信息

Stansfield Corin, Parsons Kevin J

机构信息

School of Biodiversity, One Health & Veterinary Medicine, University of Glasgow, Glasgow, United Kingdom.

出版信息

Front Cell Dev Biol. 2024 Oct 16;12:1453566. doi: 10.3389/fcell.2024.1453566. eCollection 2024.


DOI:10.3389/fcell.2024.1453566
PMID:39479512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11521891/
Abstract

Efforts to reconcile development and evolution have demonstrated that development is biased, with phenotypic variation being more readily produced in certain directions. However, how this "developmental bias" can influence micro- and macroevolution is poorly understood. In this review, we demonstrate that defining features of adaptive radiations suggest a role for developmental bias in driving adaptive divergence. These features are i) common ancestry of developmental systems; ii) rapid evolution along evolutionary "lines of least resistance;" iii) the subsequent repeated and parallel evolution of ecotypes; and iv) evolutionary change "led" by biased phenotypic plasticity upon exposure to novel environments. Drawing on empirical and theoretical data, we highlight the reciprocal relationship between development and selection as a key driver of evolutionary change, with development biasing what variation is exposed to selection, and selection acting to mold these biases to align with the adaptive landscape. Our central thesis is that developmental biases are both the causes and consequences of adaptive radiation and divergence. We argue throughout that incorporating development and developmental bias into our thinking can help to explain the exaggerated rate and scale of evolutionary processes that characterize adaptive radiations, and that this can be best achieved by using an eco-evo-devo framework incorporating evolutionary biology, development, and ecology. Such a research program would demonstrate that development is not merely a force that imposes constraints on evolution, but rather directs and is directed by evolutionary forces. We round out this review by highlighting key gaps in our understanding and suggest further research programs that can help to resolve these issues.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815a/11521891/bf876326aee9/fcell-12-1453566-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815a/11521891/c75288597fc2/fcell-12-1453566-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815a/11521891/914d9d6b3c51/fcell-12-1453566-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815a/11521891/bf876326aee9/fcell-12-1453566-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815a/11521891/c75288597fc2/fcell-12-1453566-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815a/11521891/914d9d6b3c51/fcell-12-1453566-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815a/11521891/bf876326aee9/fcell-12-1453566-g003.jpg

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[1]
Developmental lines of least resistance predict standing genetic covariation but do not constrain plasticity or rapid evolution.

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[4]
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Nat Ecol Evol. 2023-10

[5]
Developmental bias predicts 60 million years of wing shape evolution.

Proc Natl Acad Sci U S A. 2023-5-9

[6]
Shared reproductive disruption, not neural crest or tameness, explains the domestication syndrome.

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[7]
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[8]
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[9]
Repeated genetic divergence plays a minor role in repeated phenotypic divergence of lake-stream stickleback.

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