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Genetic identification of brain cell types underlying schizophrenia

With few exceptions, the marked advances in knowledge about the genetic basis of schizophrenia have not converged on findings that can be confidently used for precise experimental modeling. Applying knowledge of the cellular taxonomy of the brain from single-cell RNA-sequencing, we evaluated whether...

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Autores principales: Skene, Nathan G, Bryois, Julien, Bakken, Trygve E, Breen, Gerome, Crowley, James J, Gaspar, Héléna A, Giusti-Rodriguez, Paola, Hodge, Rebecca D, Miller, Jeremy A, Muñoz-Manchado, Ana B, O’Donovan, Michael C, Owen, Michael J, Pardiñas, Antonio F, Ryge, Jesper, Walters, James T R, Linnarsson, Sten, Lein, Ed S, Sullivan, Patrick F, Hjerling-Leffler, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477180/
https://www.ncbi.nlm.nih.gov/pubmed/29785013
http://dx.doi.org/10.1038/s41588-018-0129-5
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author Skene, Nathan G
Bryois, Julien
Bakken, Trygve E
Breen, Gerome
Crowley, James J
Gaspar, Héléna A
Giusti-Rodriguez, Paola
Hodge, Rebecca D
Miller, Jeremy A
Muñoz-Manchado, Ana B
O’Donovan, Michael C
Owen, Michael J
Pardiñas, Antonio F
Ryge, Jesper
Walters, James T R
Linnarsson, Sten
Lein, Ed S
Sullivan, Patrick F
Hjerling-Leffler, Jens
author_facet Skene, Nathan G
Bryois, Julien
Bakken, Trygve E
Breen, Gerome
Crowley, James J
Gaspar, Héléna A
Giusti-Rodriguez, Paola
Hodge, Rebecca D
Miller, Jeremy A
Muñoz-Manchado, Ana B
O’Donovan, Michael C
Owen, Michael J
Pardiñas, Antonio F
Ryge, Jesper
Walters, James T R
Linnarsson, Sten
Lein, Ed S
Sullivan, Patrick F
Hjerling-Leffler, Jens
author_sort Skene, Nathan G
collection PubMed
description With few exceptions, the marked advances in knowledge about the genetic basis of schizophrenia have not converged on findings that can be confidently used for precise experimental modeling. Applying knowledge of the cellular taxonomy of the brain from single-cell RNA-sequencing, we evaluated whether the genomic loci implicated in schizophrenia map onto specific brain cell types. We found that the common variant genomic results consistently mapped to pyramidal cells, medium spiny neurons, and certain interneurons but far less consistently to embryonic, progenitor, or glial cells. These enrichments were due to sets of genes specifically expressed in each of these cell types. We also found that many of the diverse gene sets previously associated with schizophrenia (synaptic genes, FMRP interactors, antipsychotic targets, etc.) generally implicate the same brain cell types. Our results suggest a parsimonious explanation: the common-variant genetic results for schizophrenia point at a limited set of neurons, and the gene sets point to the same cells. The genetic risk associated with medium spiny neurons did not overlap with that of glutamatergic pyramidal cells and interneurons, suggesting that different cell types have biologically distinct roles in schizophrenia.
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spelling pubmed-64771802019-04-23 Genetic identification of brain cell types underlying schizophrenia Skene, Nathan G Bryois, Julien Bakken, Trygve E Breen, Gerome Crowley, James J Gaspar, Héléna A Giusti-Rodriguez, Paola Hodge, Rebecca D Miller, Jeremy A Muñoz-Manchado, Ana B O’Donovan, Michael C Owen, Michael J Pardiñas, Antonio F Ryge, Jesper Walters, James T R Linnarsson, Sten Lein, Ed S Sullivan, Patrick F Hjerling-Leffler, Jens Nat Genet Article With few exceptions, the marked advances in knowledge about the genetic basis of schizophrenia have not converged on findings that can be confidently used for precise experimental modeling. Applying knowledge of the cellular taxonomy of the brain from single-cell RNA-sequencing, we evaluated whether the genomic loci implicated in schizophrenia map onto specific brain cell types. We found that the common variant genomic results consistently mapped to pyramidal cells, medium spiny neurons, and certain interneurons but far less consistently to embryonic, progenitor, or glial cells. These enrichments were due to sets of genes specifically expressed in each of these cell types. We also found that many of the diverse gene sets previously associated with schizophrenia (synaptic genes, FMRP interactors, antipsychotic targets, etc.) generally implicate the same brain cell types. Our results suggest a parsimonious explanation: the common-variant genetic results for schizophrenia point at a limited set of neurons, and the gene sets point to the same cells. The genetic risk associated with medium spiny neurons did not overlap with that of glutamatergic pyramidal cells and interneurons, suggesting that different cell types have biologically distinct roles in schizophrenia. 2018-05-21 2018-06 /pmc/articles/PMC6477180/ /pubmed/29785013 http://dx.doi.org/10.1038/s41588-018-0129-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Skene, Nathan G
Bryois, Julien
Bakken, Trygve E
Breen, Gerome
Crowley, James J
Gaspar, Héléna A
Giusti-Rodriguez, Paola
Hodge, Rebecca D
Miller, Jeremy A
Muñoz-Manchado, Ana B
O’Donovan, Michael C
Owen, Michael J
Pardiñas, Antonio F
Ryge, Jesper
Walters, James T R
Linnarsson, Sten
Lein, Ed S
Sullivan, Patrick F
Hjerling-Leffler, Jens
Genetic identification of brain cell types underlying schizophrenia
title Genetic identification of brain cell types underlying schizophrenia
title_full Genetic identification of brain cell types underlying schizophrenia
title_fullStr Genetic identification of brain cell types underlying schizophrenia
title_full_unstemmed Genetic identification of brain cell types underlying schizophrenia
title_short Genetic identification of brain cell types underlying schizophrenia
title_sort genetic identification of brain cell types underlying schizophrenia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477180/
https://www.ncbi.nlm.nih.gov/pubmed/29785013
http://dx.doi.org/10.1038/s41588-018-0129-5
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