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Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions
Genomic studies have identified hundreds of candidate genes near loci associated with risk for schizophrenia. To define candidates and their functions, we mutated zebrafish orthologs of 132 human schizophrenia-associated genes. We created a phenotype atlas consisting of whole-brain activity maps, br...
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Published in: | Cell 2019-04, Vol.177 (2), p.478-491.e20 |
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creator | Thyme, Summer B. Pieper, Lindsey M. Li, Eric H. Pandey, Shristi Wang, Yiqun Morris, Nathan S. Sha, Carrie Choi, Joo Won Herrera, Kristian J. Soucy, Edward R. Zimmerman, Steve Randlett, Owen Greenwood, Joel McCarroll, Steven A. Schier, Alexander F. |
description | Genomic studies have identified hundreds of candidate genes near loci associated with risk for schizophrenia. To define candidates and their functions, we mutated zebrafish orthologs of 132 human schizophrenia-associated genes. We created a phenotype atlas consisting of whole-brain activity maps, brain structural differences, and profiles of behavioral abnormalities. Phenotypes were diverse but specific, including altered forebrain development and decreased prepulse inhibition. Exploration of these datasets identified promising candidates in more than 10 gene-rich regions, including the magnesium transporter cnnm2 and the translational repressor gigyf2, and revealed shared anatomical sites of activity differences, including the pallium, hypothalamus, and tectum. Single-cell RNA sequencing uncovered an essential role for the understudied transcription factor znf536 in the development of forebrain neurons implicated in social behavior and stress. This phenotypic landscape of schizophrenia-associated genes prioritizes more than 30 candidates for further study and provides hypotheses to bridge the divide between genetic association and biological mechanism.
[Display omitted]
•132 zebrafish mutants for genes located in schizophrenia-associated genomic regions•Phenotypes for many understudied genes with previously unknown functions•Phenotype atlas for abnormal behavior and brain activity•More than 30 genes prioritized for future study
Analysis of zebrafish deficient for human schizophrenia-associated genes generates an atlas of brain and behavior phenotypes for the study of psychiatric disorders. |
doi_str_mv | 10.1016/j.cell.2019.01.048 |
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[Display omitted]
•132 zebrafish mutants for genes located in schizophrenia-associated genomic regions•Phenotypes for many understudied genes with previously unknown functions•Phenotype atlas for abnormal behavior and brain activity•More than 30 genes prioritized for future study
Analysis of zebrafish deficient for human schizophrenia-associated genes generates an atlas of brain and behavior phenotypes for the study of psychiatric disorders.</description><identifier>ISSN: 0092-8674</identifier><identifier>ISSN: 1097-4172</identifier><identifier>EISSN: 1097-4172</identifier><identifier>DOI: 10.1016/j.cell.2019.01.048</identifier><identifier>PMID: 30929901</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; behavior ; Brain ; Cerebral Cortex ; Disease Models, Animal ; forebrain ; Gene Expression Regulation - genetics ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; GWAS ; neurodevelopment ; neuropsychiatric disorder ; Phenotype ; Polymorphism, Single Nucleotide - genetics ; prepulse inhibition ; schizophrenia ; Schizophrenia - genetics ; Schizophrenia - physiopathology ; single-cell RNA-sequencing ; whole-brain activity ; zebrafish ; Zebrafish - genetics</subject><ispartof>Cell, 2019-04, Vol.177 (2), p.478-491.e20</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-f3f421fe86de793c65cb6873578458d638245435c996cf619b071ec4e295a2b23</citedby><cites>FETCH-LOGICAL-c455t-f3f421fe86de793c65cb6873578458d638245435c996cf619b071ec4e295a2b23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0092867419301114$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3547,27923,27924,45779</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30929901$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thyme, Summer B.</creatorcontrib><creatorcontrib>Pieper, Lindsey M.</creatorcontrib><creatorcontrib>Li, Eric H.</creatorcontrib><creatorcontrib>Pandey, Shristi</creatorcontrib><creatorcontrib>Wang, Yiqun</creatorcontrib><creatorcontrib>Morris, Nathan S.</creatorcontrib><creatorcontrib>Sha, Carrie</creatorcontrib><creatorcontrib>Choi, Joo Won</creatorcontrib><creatorcontrib>Herrera, Kristian J.</creatorcontrib><creatorcontrib>Soucy, Edward R.</creatorcontrib><creatorcontrib>Zimmerman, Steve</creatorcontrib><creatorcontrib>Randlett, Owen</creatorcontrib><creatorcontrib>Greenwood, Joel</creatorcontrib><creatorcontrib>McCarroll, Steven A.</creatorcontrib><creatorcontrib>Schier, Alexander F.</creatorcontrib><title>Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions</title><title>Cell</title><addtitle>Cell</addtitle><description>Genomic studies have identified hundreds of candidate genes near loci associated with risk for schizophrenia. To define candidates and their functions, we mutated zebrafish orthologs of 132 human schizophrenia-associated genes. We created a phenotype atlas consisting of whole-brain activity maps, brain structural differences, and profiles of behavioral abnormalities. Phenotypes were diverse but specific, including altered forebrain development and decreased prepulse inhibition. Exploration of these datasets identified promising candidates in more than 10 gene-rich regions, including the magnesium transporter cnnm2 and the translational repressor gigyf2, and revealed shared anatomical sites of activity differences, including the pallium, hypothalamus, and tectum. Single-cell RNA sequencing uncovered an essential role for the understudied transcription factor znf536 in the development of forebrain neurons implicated in social behavior and stress. This phenotypic landscape of schizophrenia-associated genes prioritizes more than 30 candidates for further study and provides hypotheses to bridge the divide between genetic association and biological mechanism.
[Display omitted]
•132 zebrafish mutants for genes located in schizophrenia-associated genomic regions•Phenotypes for many understudied genes with previously unknown functions•Phenotype atlas for abnormal behavior and brain activity•More than 30 genes prioritized for future study
Analysis of zebrafish deficient for human schizophrenia-associated genes generates an atlas of brain and behavior phenotypes for the study of psychiatric disorders.</description><subject>Animals</subject><subject>behavior</subject><subject>Brain</subject><subject>Cerebral Cortex</subject><subject>Disease Models, Animal</subject><subject>forebrain</subject><subject>Gene Expression Regulation - genetics</subject><subject>Genetic Predisposition to Disease</subject><subject>Genome-Wide Association Study</subject><subject>GWAS</subject><subject>neurodevelopment</subject><subject>neuropsychiatric disorder</subject><subject>Phenotype</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>prepulse inhibition</subject><subject>schizophrenia</subject><subject>Schizophrenia - genetics</subject><subject>Schizophrenia - physiopathology</subject><subject>single-cell RNA-sequencing</subject><subject>whole-brain activity</subject><subject>zebrafish</subject><subject>Zebrafish - genetics</subject><issn>0092-8674</issn><issn>1097-4172</issn><issn>1097-4172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9UU1r3DAQFSWh2ab9Az0EH3OxI8mSLEEphG2TFBZSSHoWWmkca9mVXMkbSH59ZTYNzaWnGXgfM7yH0GeCG4KJuNg0FrbbhmKiGkwazOQ7tCBYdTUjHT1CC4wVraXo2An6kPMGYyw55-_RSVsApTBZIPdzgBCnp9HbamWCy9aMUMW-urODf47jkCB4U1_mHK03E7jqGgLk6hv0fp7LovGuALkqW3U_gE_V3WBSYV7tg518DPkjOu7NNsOnl3mKfl19v1_e1Kvb6x_Ly1VtGedT3bc9o6QHKRx0qrWC27WQXcs7ybh0opWUcdZyq5SwvSBqjTsClgFV3NA1bU_R14PvuF_vwFkIUzJbPSa_M-lJR-P1WyT4QT_ERy2YYozjYnD-YpDi7z3kSe98nkM2AeI-a1qy7ojkoi1UeqDaFHNO0L-eIVjP9eiNnpV6rkdjoks9RXT274Ovkr99FMKXAwFKTI8eks7WQ7DgfAI7aRf9__z_AI5tomo</recordid><startdate>20190404</startdate><enddate>20190404</enddate><creator>Thyme, Summer B.</creator><creator>Pieper, Lindsey M.</creator><creator>Li, Eric H.</creator><creator>Pandey, Shristi</creator><creator>Wang, Yiqun</creator><creator>Morris, Nathan S.</creator><creator>Sha, Carrie</creator><creator>Choi, Joo Won</creator><creator>Herrera, Kristian J.</creator><creator>Soucy, Edward R.</creator><creator>Zimmerman, Steve</creator><creator>Randlett, Owen</creator><creator>Greenwood, Joel</creator><creator>McCarroll, Steven A.</creator><creator>Schier, Alexander F.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190404</creationdate><title>Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions</title><author>Thyme, Summer B. ; Pieper, Lindsey M. ; Li, Eric H. ; Pandey, Shristi ; Wang, Yiqun ; Morris, Nathan S. ; Sha, Carrie ; Choi, Joo Won ; Herrera, Kristian J. ; Soucy, Edward R. ; Zimmerman, Steve ; Randlett, Owen ; Greenwood, Joel ; McCarroll, Steven A. ; Schier, Alexander F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-f3f421fe86de793c65cb6873578458d638245435c996cf619b071ec4e295a2b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>behavior</topic><topic>Brain</topic><topic>Cerebral Cortex</topic><topic>Disease Models, Animal</topic><topic>forebrain</topic><topic>Gene Expression Regulation - genetics</topic><topic>Genetic Predisposition to Disease</topic><topic>Genome-Wide Association Study</topic><topic>GWAS</topic><topic>neurodevelopment</topic><topic>neuropsychiatric disorder</topic><topic>Phenotype</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>prepulse inhibition</topic><topic>schizophrenia</topic><topic>Schizophrenia - genetics</topic><topic>Schizophrenia - physiopathology</topic><topic>single-cell RNA-sequencing</topic><topic>whole-brain activity</topic><topic>zebrafish</topic><topic>Zebrafish - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thyme, Summer B.</creatorcontrib><creatorcontrib>Pieper, Lindsey M.</creatorcontrib><creatorcontrib>Li, Eric H.</creatorcontrib><creatorcontrib>Pandey, Shristi</creatorcontrib><creatorcontrib>Wang, Yiqun</creatorcontrib><creatorcontrib>Morris, Nathan S.</creatorcontrib><creatorcontrib>Sha, Carrie</creatorcontrib><creatorcontrib>Choi, Joo Won</creatorcontrib><creatorcontrib>Herrera, Kristian J.</creatorcontrib><creatorcontrib>Soucy, Edward R.</creatorcontrib><creatorcontrib>Zimmerman, Steve</creatorcontrib><creatorcontrib>Randlett, Owen</creatorcontrib><creatorcontrib>Greenwood, Joel</creatorcontrib><creatorcontrib>McCarroll, Steven A.</creatorcontrib><creatorcontrib>Schier, Alexander F.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thyme, Summer B.</au><au>Pieper, Lindsey M.</au><au>Li, Eric H.</au><au>Pandey, Shristi</au><au>Wang, Yiqun</au><au>Morris, Nathan S.</au><au>Sha, Carrie</au><au>Choi, Joo Won</au><au>Herrera, Kristian J.</au><au>Soucy, Edward R.</au><au>Zimmerman, Steve</au><au>Randlett, Owen</au><au>Greenwood, Joel</au><au>McCarroll, Steven A.</au><au>Schier, Alexander F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions</atitle><jtitle>Cell</jtitle><addtitle>Cell</addtitle><date>2019-04-04</date><risdate>2019</risdate><volume>177</volume><issue>2</issue><spage>478</spage><epage>491.e20</epage><pages>478-491.e20</pages><issn>0092-8674</issn><issn>1097-4172</issn><eissn>1097-4172</eissn><abstract>Genomic studies have identified hundreds of candidate genes near loci associated with risk for schizophrenia. To define candidates and their functions, we mutated zebrafish orthologs of 132 human schizophrenia-associated genes. We created a phenotype atlas consisting of whole-brain activity maps, brain structural differences, and profiles of behavioral abnormalities. Phenotypes were diverse but specific, including altered forebrain development and decreased prepulse inhibition. Exploration of these datasets identified promising candidates in more than 10 gene-rich regions, including the magnesium transporter cnnm2 and the translational repressor gigyf2, and revealed shared anatomical sites of activity differences, including the pallium, hypothalamus, and tectum. Single-cell RNA sequencing uncovered an essential role for the understudied transcription factor znf536 in the development of forebrain neurons implicated in social behavior and stress. This phenotypic landscape of schizophrenia-associated genes prioritizes more than 30 candidates for further study and provides hypotheses to bridge the divide between genetic association and biological mechanism.
[Display omitted]
•132 zebrafish mutants for genes located in schizophrenia-associated genomic regions•Phenotypes for many understudied genes with previously unknown functions•Phenotype atlas for abnormal behavior and brain activity•More than 30 genes prioritized for future study
Analysis of zebrafish deficient for human schizophrenia-associated genes generates an atlas of brain and behavior phenotypes for the study of psychiatric disorders.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30929901</pmid><doi>10.1016/j.cell.2019.01.048</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals behavior Brain Cerebral Cortex Disease Models, Animal forebrain Gene Expression Regulation - genetics Genetic Predisposition to Disease Genome-Wide Association Study GWAS neurodevelopment neuropsychiatric disorder Phenotype Polymorphism, Single Nucleotide - genetics prepulse inhibition schizophrenia Schizophrenia - genetics Schizophrenia - physiopathology single-cell RNA-sequencing whole-brain activity zebrafish Zebrafish - genetics |
title | Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions |
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