One-step generation of triple gene-targeted pigs using CRISPR/Cas9 system
Pig shows multiple superior characteristics in anatomy, physiology, and genome that have made this species to be more suitable models for human diseases, especially for neurodegenerative diseases, because they have similar cerebral convolutions compared with human neocortex. Recently, CRISPR/Cas9 sy...
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creator | Wang, Xianlong Cao, Chunwei Huang, Jiaojiao Yao, Jing Hai, Tang Zheng, Qiantao Wang, Xiao Zhang, Hongyong Qin, Guosong Cheng, Jinbo Wang, Yanfang Yuan, Zengqiang Zhou, Qi Wang, Hongmei Zhao, Jianguo |
description | Pig shows multiple superior characteristics in anatomy, physiology, and genome that have made this species to be more suitable models for human diseases, especially for neurodegenerative diseases, because they have similar cerebral convolutions compared with human neocortex. Recently, CRISPR/Cas9 system shows enormous potential for engineering the pig genome. In this study, we expect to generate human Parkinson’s disease pig model using CRISPR/Cas9 system by simultaneously targeting three distinct genomic loci, parkin/DJ-1/
PINK1
, in Bama miniature pigs. By co-injection of Cas9 mRNA and multiplexing single guide RNAs (sgRNAs) targeting
parkin, DJ-1
, and
PINK1
genes, respectively, into
in vivo
derived pronuclear embryos, we simultaneously targeted three distinct genomic loci. The gene modified piglets remain healthy and display normal behavior at the age of 10 months. In addition, despite the high number of sgRNAs were employed in the present study, our trio-based whole-genome sequencing analysis suggested that the incidence of off-target events is low. Our results demonstrate that the simplicity, efficiency, and power of the CRISPR/Cas9 system to allow for the modification of multiple genes in pigs and yield results of high medical value. |
doi_str_mv | 10.1038/srep20620 |
format | Article |
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PINK1
, in Bama miniature pigs. By co-injection of Cas9 mRNA and multiplexing single guide RNAs (sgRNAs) targeting
parkin, DJ-1
, and
PINK1
genes, respectively, into
in vivo
derived pronuclear embryos, we simultaneously targeted three distinct genomic loci. The gene modified piglets remain healthy and display normal behavior at the age of 10 months. In addition, despite the high number of sgRNAs were employed in the present study, our trio-based whole-genome sequencing analysis suggested that the incidence of off-target events is low. Our results demonstrate that the simplicity, efficiency, and power of the CRISPR/Cas9 system to allow for the modification of multiple genes in pigs and yield results of high medical value.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep20620</identifier><identifier>PMID: 26857844</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45/70 ; 631/1647/1511 ; 631/1647/1513/1967/3196 ; Anatomy ; Animal models ; Animals ; Animals, Genetically Modified - genetics ; CRISPR ; CRISPR-Cas Systems ; Disease Models, Animal ; Embryos ; Gene loci ; Gene Targeting - methods ; Genetic Loci ; Genomes ; Hogs ; Humanities and Social Sciences ; Humans ; Movement disorders ; mRNA ; multidisciplinary ; Neocortex ; Neurodegenerative diseases ; PARK7 protein ; Parkin protein ; Parkinson Disease - genetics ; Parkinson Disease - metabolism ; Parkinson's disease ; Protein Deglycase DJ-1 - genetics ; Protein Deglycase DJ-1 - metabolism ; Protein Kinases - genetics ; Protein Kinases - metabolism ; PTEN-induced putative kinase ; Science ; Swine ; Ubiquitin-Protein Ligases - genetics ; Ubiquitin-Protein Ligases - metabolism</subject><ispartof>Scientific reports, 2016-02, Vol.6 (1), p.20620-20620, Article 20620</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Feb 2016</rights><rights>Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-e7e6d80c74287b552accfa11fcb362e5f91ef4828483f650c4140a2f1f7e2e8d3</citedby><cites>FETCH-LOGICAL-c504t-e7e6d80c74287b552accfa11fcb362e5f91ef4828483f650c4140a2f1f7e2e8d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746670/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746670/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,27931,27932,41127,42196,51583,53798,53800</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26857844$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Xianlong</creatorcontrib><creatorcontrib>Cao, Chunwei</creatorcontrib><creatorcontrib>Huang, Jiaojiao</creatorcontrib><creatorcontrib>Yao, Jing</creatorcontrib><creatorcontrib>Hai, Tang</creatorcontrib><creatorcontrib>Zheng, Qiantao</creatorcontrib><creatorcontrib>Wang, Xiao</creatorcontrib><creatorcontrib>Zhang, Hongyong</creatorcontrib><creatorcontrib>Qin, Guosong</creatorcontrib><creatorcontrib>Cheng, Jinbo</creatorcontrib><creatorcontrib>Wang, Yanfang</creatorcontrib><creatorcontrib>Yuan, Zengqiang</creatorcontrib><creatorcontrib>Zhou, Qi</creatorcontrib><creatorcontrib>Wang, Hongmei</creatorcontrib><creatorcontrib>Zhao, Jianguo</creatorcontrib><title>One-step generation of triple gene-targeted pigs using CRISPR/Cas9 system</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Pig shows multiple superior characteristics in anatomy, physiology, and genome that have made this species to be more suitable models for human diseases, especially for neurodegenerative diseases, because they have similar cerebral convolutions compared with human neocortex. Recently, CRISPR/Cas9 system shows enormous potential for engineering the pig genome. In this study, we expect to generate human Parkinson’s disease pig model using CRISPR/Cas9 system by simultaneously targeting three distinct genomic loci, parkin/DJ-1/
PINK1
, in Bama miniature pigs. By co-injection of Cas9 mRNA and multiplexing single guide RNAs (sgRNAs) targeting
parkin, DJ-1
, and
PINK1
genes, respectively, into
in vivo
derived pronuclear embryos, we simultaneously targeted three distinct genomic loci. The gene modified piglets remain healthy and display normal behavior at the age of 10 months. In addition, despite the high number of sgRNAs were employed in the present study, our trio-based whole-genome sequencing analysis suggested that the incidence of off-target events is low. Our results demonstrate that the simplicity, efficiency, and power of the CRISPR/Cas9 system to allow for the modification of multiple genes in pigs and yield results of high medical value.</description><subject>45/70</subject><subject>631/1647/1511</subject><subject>631/1647/1513/1967/3196</subject><subject>Anatomy</subject><subject>Animal models</subject><subject>Animals</subject><subject>Animals, Genetically Modified - genetics</subject><subject>CRISPR</subject><subject>CRISPR-Cas Systems</subject><subject>Disease Models, Animal</subject><subject>Embryos</subject><subject>Gene loci</subject><subject>Gene Targeting - methods</subject><subject>Genetic Loci</subject><subject>Genomes</subject><subject>Hogs</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Movement disorders</subject><subject>mRNA</subject><subject>multidisciplinary</subject><subject>Neocortex</subject><subject>Neurodegenerative diseases</subject><subject>PARK7 protein</subject><subject>Parkin protein</subject><subject>Parkinson Disease - genetics</subject><subject>Parkinson Disease - metabolism</subject><subject>Parkinson's disease</subject><subject>Protein Deglycase DJ-1 - genetics</subject><subject>Protein Deglycase DJ-1 - metabolism</subject><subject>Protein Kinases - genetics</subject><subject>Protein Kinases - metabolism</subject><subject>PTEN-induced putative kinase</subject><subject>Science</subject><subject>Swine</subject><subject>Ubiquitin-Protein Ligases - genetics</subject><subject>Ubiquitin-Protein Ligases - metabolism</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplkV1LwzAUhoMoOqYX_gEpeKNCXZImaXojyPBjICh-XIcsO6kdXVqTVti_NzodU3OTcM7Dc054ETok-JzgTI6Ch5ZiQfEWGlDMeEozSrc33nvoIIQ5jofTgpFiF-1RIXkuGRugyb2DNHTQJiU48LqrGpc0Nul81dbwVUw77UvoYJa0VRmSPlSuTMaPk6eHx9FYhyIJyyhY7KMdq-sAB9_3EL1cXz2Pb9O7-5vJ-PIuNRyzLoUcxExikzMq8ynnVBtjNSHWTDNBgduCgGWSSiYzKzg2jDCsqSU2Bwpylg3Rxcrb9tMFzAy4zutatb5aaL9Uja7U746rXlXZvCuWMyFyHAUn3wLfvPUQOrWogoG61g6aPiiSC5YxknER0eM_6LzpvYvfU0QWBSYCSxKp0xVlfBNiHHa9DMHqMyO1ziiyR5vbr8mfRCJwtgJCbLkS_MbIf7YPSHKaXQ</recordid><startdate>20160209</startdate><enddate>20160209</enddate><creator>Wang, Xianlong</creator><creator>Cao, Chunwei</creator><creator>Huang, Jiaojiao</creator><creator>Yao, Jing</creator><creator>Hai, Tang</creator><creator>Zheng, Qiantao</creator><creator>Wang, Xiao</creator><creator>Zhang, Hongyong</creator><creator>Qin, Guosong</creator><creator>Cheng, Jinbo</creator><creator>Wang, Yanfang</creator><creator>Yuan, Zengqiang</creator><creator>Zhou, Qi</creator><creator>Wang, Hongmei</creator><creator>Zhao, Jianguo</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160209</creationdate><title>One-step generation of triple gene-targeted pigs using CRISPR/Cas9 system</title><author>Wang, Xianlong ; Cao, Chunwei ; Huang, Jiaojiao ; Yao, Jing ; Hai, Tang ; Zheng, Qiantao ; Wang, Xiao ; Zhang, Hongyong ; Qin, Guosong ; Cheng, Jinbo ; Wang, Yanfang ; Yuan, Zengqiang ; Zhou, Qi ; Wang, Hongmei ; Zhao, Jianguo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-e7e6d80c74287b552accfa11fcb362e5f91ef4828483f650c4140a2f1f7e2e8d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>45/70</topic><topic>631/1647/1511</topic><topic>631/1647/1513/1967/3196</topic><topic>Anatomy</topic><topic>Animal models</topic><topic>Animals</topic><topic>Animals, Genetically Modified - genetics</topic><topic>CRISPR</topic><topic>CRISPR-Cas Systems</topic><topic>Disease Models, Animal</topic><topic>Embryos</topic><topic>Gene loci</topic><topic>Gene Targeting - methods</topic><topic>Genetic Loci</topic><topic>Genomes</topic><topic>Hogs</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Movement disorders</topic><topic>mRNA</topic><topic>multidisciplinary</topic><topic>Neocortex</topic><topic>Neurodegenerative diseases</topic><topic>PARK7 protein</topic><topic>Parkin protein</topic><topic>Parkinson Disease - genetics</topic><topic>Parkinson Disease - metabolism</topic><topic>Parkinson's disease</topic><topic>Protein Deglycase DJ-1 - genetics</topic><topic>Protein Deglycase DJ-1 - metabolism</topic><topic>Protein Kinases - genetics</topic><topic>Protein Kinases - metabolism</topic><topic>PTEN-induced putative kinase</topic><topic>Science</topic><topic>Swine</topic><topic>Ubiquitin-Protein Ligases - genetics</topic><topic>Ubiquitin-Protein Ligases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Xianlong</creatorcontrib><creatorcontrib>Cao, Chunwei</creatorcontrib><creatorcontrib>Huang, Jiaojiao</creatorcontrib><creatorcontrib>Yao, Jing</creatorcontrib><creatorcontrib>Hai, Tang</creatorcontrib><creatorcontrib>Zheng, Qiantao</creatorcontrib><creatorcontrib>Wang, Xiao</creatorcontrib><creatorcontrib>Zhang, Hongyong</creatorcontrib><creatorcontrib>Qin, Guosong</creatorcontrib><creatorcontrib>Cheng, Jinbo</creatorcontrib><creatorcontrib>Wang, Yanfang</creatorcontrib><creatorcontrib>Yuan, Zengqiang</creatorcontrib><creatorcontrib>Zhou, Qi</creatorcontrib><creatorcontrib>Wang, Hongmei</creatorcontrib><creatorcontrib>Zhao, Jianguo</creatorcontrib><collection>Springer Nature OA/Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Xianlong</au><au>Cao, Chunwei</au><au>Huang, Jiaojiao</au><au>Yao, Jing</au><au>Hai, Tang</au><au>Zheng, Qiantao</au><au>Wang, Xiao</au><au>Zhang, Hongyong</au><au>Qin, Guosong</au><au>Cheng, Jinbo</au><au>Wang, Yanfang</au><au>Yuan, Zengqiang</au><au>Zhou, Qi</au><au>Wang, Hongmei</au><au>Zhao, Jianguo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>One-step generation of triple gene-targeted pigs using CRISPR/Cas9 system</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2016-02-09</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><spage>20620</spage><epage>20620</epage><pages>20620-20620</pages><artnum>20620</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Pig shows multiple superior characteristics in anatomy, physiology, and genome that have made this species to be more suitable models for human diseases, especially for neurodegenerative diseases, because they have similar cerebral convolutions compared with human neocortex. Recently, CRISPR/Cas9 system shows enormous potential for engineering the pig genome. In this study, we expect to generate human Parkinson’s disease pig model using CRISPR/Cas9 system by simultaneously targeting three distinct genomic loci, parkin/DJ-1/
PINK1
, in Bama miniature pigs. By co-injection of Cas9 mRNA and multiplexing single guide RNAs (sgRNAs) targeting
parkin, DJ-1
, and
PINK1
genes, respectively, into
in vivo
derived pronuclear embryos, we simultaneously targeted three distinct genomic loci. The gene modified piglets remain healthy and display normal behavior at the age of 10 months. In addition, despite the high number of sgRNAs were employed in the present study, our trio-based whole-genome sequencing analysis suggested that the incidence of off-target events is low. Our results demonstrate that the simplicity, efficiency, and power of the CRISPR/Cas9 system to allow for the modification of multiple genes in pigs and yield results of high medical value.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26857844</pmid><doi>10.1038/srep20620</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 45/70 631/1647/1511 631/1647/1513/1967/3196 Anatomy Animal models Animals Animals, Genetically Modified - genetics CRISPR CRISPR-Cas Systems Disease Models, Animal Embryos Gene loci Gene Targeting - methods Genetic Loci Genomes Hogs Humanities and Social Sciences Humans Movement disorders mRNA multidisciplinary Neocortex Neurodegenerative diseases PARK7 protein Parkin protein Parkinson Disease - genetics Parkinson Disease - metabolism Parkinson's disease Protein Deglycase DJ-1 - genetics Protein Deglycase DJ-1 - metabolism Protein Kinases - genetics Protein Kinases - metabolism PTEN-induced putative kinase Science Swine Ubiquitin-Protein Ligases - genetics Ubiquitin-Protein Ligases - metabolism |
title | One-step generation of triple gene-targeted pigs using CRISPR/Cas9 system |
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