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PEA15 loss of function and defective cerebral development in the domestic cat

Cerebral cortical size and organization are critical features of neurodevelopment and human evolution, for which genetic investigation in model organisms can provide insight into developmental mechanisms and the causes of cerebral malformations. However, some abnormalities in cerebral cortical proli...

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Autores principales: Graff, Emily C., Cochran, J. Nicholas, Kaelin, Christopher B., Day, Kenneth, Gray-Edwards, Heather L., Watanabe, Rie, Koehler, Jey W., Falgoust, Rebecca A., Prokop, Jeremy W., Myers, Richard M., Cox, Nancy R., Barsh, Gregory S., Martin, Douglas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723247/
https://www.ncbi.nlm.nih.gov/pubmed/33290415
http://dx.doi.org/10.1371/journal.pgen.1008671
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author Graff, Emily C.
Cochran, J. Nicholas
Kaelin, Christopher B.
Day, Kenneth
Gray-Edwards, Heather L.
Watanabe, Rie
Koehler, Jey W.
Falgoust, Rebecca A.
Prokop, Jeremy W.
Myers, Richard M.
Cox, Nancy R.
Barsh, Gregory S.
Martin, Douglas R.
author_facet Graff, Emily C.
Cochran, J. Nicholas
Kaelin, Christopher B.
Day, Kenneth
Gray-Edwards, Heather L.
Watanabe, Rie
Koehler, Jey W.
Falgoust, Rebecca A.
Prokop, Jeremy W.
Myers, Richard M.
Cox, Nancy R.
Barsh, Gregory S.
Martin, Douglas R.
author_sort Graff, Emily C.
collection PubMed
description Cerebral cortical size and organization are critical features of neurodevelopment and human evolution, for which genetic investigation in model organisms can provide insight into developmental mechanisms and the causes of cerebral malformations. However, some abnormalities in cerebral cortical proliferation and folding are challenging to study in laboratory mice due to the absence of gyri and sulci in rodents. We report an autosomal recessive allele in domestic cats associated with impaired cerebral cortical expansion and folding, giving rise to a smooth, lissencephalic brain, and that appears to be caused by homozygosity for a frameshift in PEA15 (phosphoprotein expressed in astrocytes-15). Notably, previous studies of a Pea15 targeted mutation in mice did not reveal structural brain abnormalities. Affected cats, however, present with a non-progressive hypermetric gait and tremors, develop dissociative behavioral defects and aggression with age, and exhibit profound malformation of the cerebrum, with a 45% average decrease in overall brain weight, and reduction or absence of the ectosylvian, sylvian and anterior cingulate gyrus. Histologically, the cerebral cortical layers are disorganized, there is substantial loss of white matter in tracts such as the corona radiata and internal capsule, but the cerebellum is relatively spared. RNA-seq and immunohistochemical analysis reveal astrocytosis. Fibroblasts cultured from affected cats exhibit increased TNFα-mediated apoptosis, and increased FGFb-induced proliferation, consistent with previous studies implicating PEA15 as an intracellular adapter protein, and suggesting an underlying pathophysiology in which increased death of neurons accompanied by increased proliferation of astrocytes gives rise to abnormal organization of neuronal layers and loss of white matter. Taken together, our work points to a new role for PEA15 in development of a complex cerebral cortex that is only apparent in gyrencephalic species.
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spelling pubmed-77232472020-12-16 PEA15 loss of function and defective cerebral development in the domestic cat Graff, Emily C. Cochran, J. Nicholas Kaelin, Christopher B. Day, Kenneth Gray-Edwards, Heather L. Watanabe, Rie Koehler, Jey W. Falgoust, Rebecca A. Prokop, Jeremy W. Myers, Richard M. Cox, Nancy R. Barsh, Gregory S. Martin, Douglas R. PLoS Genet Research Article Cerebral cortical size and organization are critical features of neurodevelopment and human evolution, for which genetic investigation in model organisms can provide insight into developmental mechanisms and the causes of cerebral malformations. However, some abnormalities in cerebral cortical proliferation and folding are challenging to study in laboratory mice due to the absence of gyri and sulci in rodents. We report an autosomal recessive allele in domestic cats associated with impaired cerebral cortical expansion and folding, giving rise to a smooth, lissencephalic brain, and that appears to be caused by homozygosity for a frameshift in PEA15 (phosphoprotein expressed in astrocytes-15). Notably, previous studies of a Pea15 targeted mutation in mice did not reveal structural brain abnormalities. Affected cats, however, present with a non-progressive hypermetric gait and tremors, develop dissociative behavioral defects and aggression with age, and exhibit profound malformation of the cerebrum, with a 45% average decrease in overall brain weight, and reduction or absence of the ectosylvian, sylvian and anterior cingulate gyrus. Histologically, the cerebral cortical layers are disorganized, there is substantial loss of white matter in tracts such as the corona radiata and internal capsule, but the cerebellum is relatively spared. RNA-seq and immunohistochemical analysis reveal astrocytosis. Fibroblasts cultured from affected cats exhibit increased TNFα-mediated apoptosis, and increased FGFb-induced proliferation, consistent with previous studies implicating PEA15 as an intracellular adapter protein, and suggesting an underlying pathophysiology in which increased death of neurons accompanied by increased proliferation of astrocytes gives rise to abnormal organization of neuronal layers and loss of white matter. Taken together, our work points to a new role for PEA15 in development of a complex cerebral cortex that is only apparent in gyrencephalic species. Public Library of Science 2020-12-08 /pmc/articles/PMC7723247/ /pubmed/33290415 http://dx.doi.org/10.1371/journal.pgen.1008671 Text en © 2020 Graff et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Graff, Emily C.
Cochran, J. Nicholas
Kaelin, Christopher B.
Day, Kenneth
Gray-Edwards, Heather L.
Watanabe, Rie
Koehler, Jey W.
Falgoust, Rebecca A.
Prokop, Jeremy W.
Myers, Richard M.
Cox, Nancy R.
Barsh, Gregory S.
Martin, Douglas R.
PEA15 loss of function and defective cerebral development in the domestic cat
title PEA15 loss of function and defective cerebral development in the domestic cat
title_full PEA15 loss of function and defective cerebral development in the domestic cat
title_fullStr PEA15 loss of function and defective cerebral development in the domestic cat
title_full_unstemmed PEA15 loss of function and defective cerebral development in the domestic cat
title_short PEA15 loss of function and defective cerebral development in the domestic cat
title_sort pea15 loss of function and defective cerebral development in the domestic cat
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723247/
https://www.ncbi.nlm.nih.gov/pubmed/33290415
http://dx.doi.org/10.1371/journal.pgen.1008671
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