Genetic mechanisms control the linear scaling between related cortical primary and higher order sensory areas

In mammals, the neocortical layout consists of few modality-specific primary sensory areas and a multitude of higher order ones. Abnormal layout of cortical areas may disrupt sensory function and behavior. Developmental genetic mechanisms specify primary areas, but mechanisms influencing higher orde...

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Published in:eLife Vol. 4
Main Authors: Zembrzycki, Andreas, Stocker, Adam M, Leingärtner, Axel, Sahara, Setsuko, Chou, Shen-Ju, Kalatsky, Valery, May, Scott R, Stryker, Michael P, O'Leary, Dennis Dm
Format: Journal Article
Language:English
Published: England eLife Science Publications, Ltd 24-12-2015
eLife Sciences Publications Ltd
eLife Sciences Publications, Ltd
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Summary:In mammals, the neocortical layout consists of few modality-specific primary sensory areas and a multitude of higher order ones. Abnormal layout of cortical areas may disrupt sensory function and behavior. Developmental genetic mechanisms specify primary areas, but mechanisms influencing higher order area properties are unknown. By exploiting gain-of and loss-of function mouse models of the transcription factor Emx2, we have generated bi-directional changes in primary visual cortex size in vivo and have used it as a model to show a novel and prominent function for genetic mechanisms regulating primary visual area size and also proportionally dictating the sizes of surrounding higher order visual areas. This finding redefines the role for intrinsic genetic mechanisms to concomitantly specify and scale primary and related higher order sensory areas in a linear fashion.
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These authors contributed equally to this work.
Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
University Cancer Center Hamburg, University Medical Center, Hamburg, Germany.
MRC Centre for Developmental Neurobiology, Kings College, London, United Kingdom.
Biosciences Department, Minnesota State University, Moorhead, United States.
Enthought Inc, Austin, United States.
ISSN:2050-084X
2050-084X
DOI:10.7554/eLife.11416