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Genetic and phylogenetic uncoupling of structure and function in human transmodal cortex

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Valk,  Sofie L.
Otto Hahn Group Cognitive Neurogenetics, MPI for Human Cognitive and Brain Sciences, Max Planck Society;
Institute of Neuroscience and Medicine, Research Center Jülich, Germany;
Institute of Systems Neuroscience, Heinrich Heine University Düsseldorf, Germany;

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Bayrak,  Seyma
Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Citation

Valk, S. L., Xu, T., Paquola, C., Park, B.-y., Bethlehem, R. A. I., Vos de Wael, R., et al. (2022). Genetic and phylogenetic uncoupling of structure and function in human transmodal cortex. Nature Communications, 13(1): 2341. doi:10.1038/s41467-022-29886-1.


Cite as: https://hdl.handle.net/21.11116/0000-000A-7B08-4
Abstract
Brain structure scaffolds intrinsic function, supporting cognition and ultimately behavioral flexibility. However, it remains unclear how a static, genetically controlled architecture supports flexible cognition and behavior. Here, we synthesize genetic, phylogenetic and cognitive analyses to understand how the macroscale organization of structure-function coupling across the cortex can inform its role in cognition. In humans, structure-function coupling was highest in regions of unimodal cortex and lowest in transmodal cortex, a pattern that was mirrored by a reduced alignment with heritable connectivity profiles. Structure-function uncoupling in macaques had a similar spatial distribution, but we observed an increased coupling between structure and function in association cortices relative to humans. Meta-analysis suggested regions with the least genetic control (low heritable correspondence and different across primates) are linked to social-cognition and autobiographical memory. Our findings suggest that genetic and evolutionary uncoupling of structure and function in different transmodal systems may support the emergence of complex forms of cognition.