Abstract
How genes interact with the environment to shape phenotypic variation and evolution is a fundamental question interesting to biologists from various fields. Existing linear models built on single genes are inadequate to reveal the complexity of gene-environment (G-E) interactions. Here, we develop a conceptual model for mechanistically dissecting G-E interplay by integrating previously disconnected theories and methods. Under this integration, evolutionary game theory, developmental modularity theory, and variable selection method allow us to reconstruct environment-induced, maximally informative, sparse, and casual multilayer genetic networks. We design and conduct a mapping experiment using a salt-resistant tree species to validate the biological application of the new model. The model identifies previously uncharacterized molecular mechanisms that mediate trees’ response to saline stress. Our model provides a tool to comprehend the genetic architecture of trait variation and evolution and trace the information flow of each gene toward phenotypes within omnigenic networks.
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