Inducible Transgene Expression in Human iPS Cells Using Versatile All-in-One piggyBac Transposons
Transgenics is a mainstay of functional genomics. Conditionally overexpressing genes of interest (GOIs) helps to reveal their roles in the control of complex biological processes. Complemented by findings in classic animal model systems, recent advances in human embryonic stem cell (hESC) and patien...
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container_title | Induced Pluripotent Stem (iPS) Cells |
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creator | Kim, Shin-Il Oceguera-Yanez, Fabian Sakurai, Chiho Nakagawa, Masato Yamanaka, Shinya Woltjen, Knut |
description | Transgenics is a mainstay of functional genomics. Conditionally overexpressing genes of interest (GOIs) helps to reveal their roles in the control of complex biological processes. Complemented by findings in classic animal model systems, recent advances in human embryonic stem cell (hESC) and patient-specific induced pluripotent stem cell (hiPSC) differentiation have led to sophisticated in vitro models of human development and disease. Yet, as transgenic elements encoding inducible systems must be introduced de novo into each genetically unique human stem cell line, robust and straightforward solutions to gene delivery are required. Transposons are a family of mobile DNA elements that have been adapted as experimental tools for stable genomic integration of transgenes. The piggyBac (PB) transposon from Trichoplusia ni presents a number of benefits over classic viral or BAC transgenesis: ease of application, simple integration-site mapping, and the unique capacity for traceless excision. Moreover, their large capacity permits the consolidation of multiple transgene components in a single vector system. In this chapter, we outline the features of a panel of “All-in-One” PB transposons designed for drug-inducible gene expression and provide guidelines to establish and validate populations or clones of transgenic hiPSCs. |
doi_str_mv | 10.1007/7651_2015_251 |
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Conditionally overexpressing genes of interest (GOIs) helps to reveal their roles in the control of complex biological processes. Complemented by findings in classic animal model systems, recent advances in human embryonic stem cell (hESC) and patient-specific induced pluripotent stem cell (hiPSC) differentiation have led to sophisticated in vitro models of human development and disease. Yet, as transgenic elements encoding inducible systems must be introduced de novo into each genetically unique human stem cell line, robust and straightforward solutions to gene delivery are required. Transposons are a family of mobile DNA elements that have been adapted as experimental tools for stable genomic integration of transgenes. The piggyBac (PB) transposon from Trichoplusia ni presents a number of benefits over classic viral or BAC transgenesis: ease of application, simple integration-site mapping, and the unique capacity for traceless excision. Moreover, their large capacity permits the consolidation of multiple transgene components in a single vector system. 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Conditionally overexpressing genes of interest (GOIs) helps to reveal their roles in the control of complex biological processes. Complemented by findings in classic animal model systems, recent advances in human embryonic stem cell (hESC) and patient-specific induced pluripotent stem cell (hiPSC) differentiation have led to sophisticated in vitro models of human development and disease. Yet, as transgenic elements encoding inducible systems must be introduced de novo into each genetically unique human stem cell line, robust and straightforward solutions to gene delivery are required. Transposons are a family of mobile DNA elements that have been adapted as experimental tools for stable genomic integration of transgenes. The piggyBac (PB) transposon from Trichoplusia ni presents a number of benefits over classic viral or BAC transgenesis: ease of application, simple integration-site mapping, and the unique capacity for traceless excision. Moreover, their large capacity permits the consolidation of multiple transgene components in a single vector system. In this chapter, we outline the features of a panel of “All-in-One” PB transposons designed for drug-inducible gene expression and provide guidelines to establish and validate populations or clones of transgenic hiPSCs.</description><subject>Cell Culture Techniques - methods</subject><subject>Cell Separation - methods</subject><subject>Cell Tracking - methods</subject><subject>Cells, Cultured</subject><subject>Cellular Reprogramming</subject><subject>Cellular Reprogramming Techniques - methods</subject><subject>Clone Cells - cytology</subject><subject>DNA Transposable Elements - genetics</subject><subject>Doxycycline - pharmacology</subject><subject>Doxycycline regulated</subject><subject>Fibroblasts - cytology</subject><subject>Gene expression</subject><subject>Gene Expression - drug effects</subject><subject>Gene Expression - genetics</subject><subject>Genes, Reporter</subject><subject>Genetic Vectors - genetics</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Human induced pluripotent stem cell (hiPSC)</subject><subject>Humans</subject><subject>Induced Pluripotent Stem Cells - cytology</subject><subject>Induced Pluripotent Stem Cells - metabolism</subject><subject>Luciferases - genetics</subject><subject>Luminescent Proteins - genetics</subject><subject>Neomycin - pharmacology</subject><subject>Puromycin - pharmacology</subject><subject>Red Fluorescent Protein</subject><subject>Reprogramming</subject><subject>Stable transgenesis</subject><subject>Transgenes - genetics</subject><subject>Transposon</subject><issn>1064-3745</issn><issn>1940-6029</issn><isbn>9781493930548</isbn><isbn>1493930540</isbn><isbn>9781493930555</isbn><isbn>1493930559</isbn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUMtKw0AUHV_YUrt0K9lL9N7MK1nWUrVQqGDrdphMJmE0nYSMBfv3jlQXru6B8-CeQ8g1wh0CyHspOKoMkKuM4wmZFjJHVtCCAuf8lIyxYJAKyIqzfxzLzyMHgqVUMj4i0xDeAQAFF5nESzLKoidiGBO99NXeuLK1yWbQPjTW22Tx1Q82BNf5xPnkeb_TEby8JnPbtiHZBueb5M0OQX-66Ju1bep8uo7G3jXN4UGbY1bfhc6HK3JR6zbY6e-dkO3jYjN_Tlfrp-V8tkpNxiim8XVmKskQdS6QGYkcEGleoRCmhhptVbDaCl7XFkrIJGha5aIWhpq80CWdkJtjbr8vd7ZS_eB2ejiov65RcHsUhEj5xg6q7LqPoBDUz9jq39j0G8TDaNg</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Kim, Shin-Il</creator><creator>Oceguera-Yanez, Fabian</creator><creator>Sakurai, Chiho</creator><creator>Nakagawa, Masato</creator><creator>Yamanaka, Shinya</creator><creator>Woltjen, Knut</creator><general>Springer New York</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20160101</creationdate><title>Inducible Transgene Expression in Human iPS Cells Using Versatile All-in-One piggyBac Transposons</title><author>Kim, Shin-Il ; Oceguera-Yanez, Fabian ; Sakurai, Chiho ; Nakagawa, Masato ; Yamanaka, Shinya ; Woltjen, Knut</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2431-4934cd7411a8614c71501138d166cf0f1ed94fe65ffe0b0270a3d86f6c3c89ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cell Culture Techniques - methods</topic><topic>Cell Separation - methods</topic><topic>Cell Tracking - methods</topic><topic>Cells, Cultured</topic><topic>Cellular Reprogramming</topic><topic>Cellular Reprogramming Techniques - methods</topic><topic>Clone Cells - cytology</topic><topic>DNA Transposable Elements - genetics</topic><topic>Doxycycline - pharmacology</topic><topic>Doxycycline regulated</topic><topic>Fibroblasts - cytology</topic><topic>Gene expression</topic><topic>Gene Expression - drug effects</topic><topic>Gene Expression - genetics</topic><topic>Genes, Reporter</topic><topic>Genetic Vectors - genetics</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Human induced pluripotent stem cell (hiPSC)</topic><topic>Humans</topic><topic>Induced Pluripotent Stem Cells - cytology</topic><topic>Induced Pluripotent Stem Cells - metabolism</topic><topic>Luciferases - genetics</topic><topic>Luminescent Proteins - genetics</topic><topic>Neomycin - pharmacology</topic><topic>Puromycin - pharmacology</topic><topic>Red Fluorescent Protein</topic><topic>Reprogramming</topic><topic>Stable transgenesis</topic><topic>Transgenes - genetics</topic><topic>Transposon</topic><toplevel>online_resources</toplevel><creatorcontrib>Kim, Shin-Il</creatorcontrib><creatorcontrib>Oceguera-Yanez, Fabian</creatorcontrib><creatorcontrib>Sakurai, Chiho</creatorcontrib><creatorcontrib>Nakagawa, Masato</creatorcontrib><creatorcontrib>Yamanaka, Shinya</creatorcontrib><creatorcontrib>Woltjen, Knut</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Induced Pluripotent Stem (iPS) Cells</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Shin-Il</au><au>Oceguera-Yanez, Fabian</au><au>Sakurai, Chiho</au><au>Nakagawa, Masato</au><au>Yamanaka, Shinya</au><au>Woltjen, Knut</au><au>Turksen, Kursad</au><au>Nagy, Andras</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inducible Transgene Expression in Human iPS Cells Using Versatile All-in-One piggyBac Transposons</atitle><jtitle>Induced Pluripotent Stem (iPS) Cells</jtitle><addtitle>Methods Mol Biol</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>1357</volume><spage>111</spage><epage>131</epage><pages>111-131</pages><issn>1064-3745</issn><eissn>1940-6029</eissn><isbn>9781493930548</isbn><isbn>1493930540</isbn><eisbn>9781493930555</eisbn><eisbn>1493930559</eisbn><abstract>Transgenics is a mainstay of functional genomics. Conditionally overexpressing genes of interest (GOIs) helps to reveal their roles in the control of complex biological processes. Complemented by findings in classic animal model systems, recent advances in human embryonic stem cell (hESC) and patient-specific induced pluripotent stem cell (hiPSC) differentiation have led to sophisticated in vitro models of human development and disease. Yet, as transgenic elements encoding inducible systems must be introduced de novo into each genetically unique human stem cell line, robust and straightforward solutions to gene delivery are required. Transposons are a family of mobile DNA elements that have been adapted as experimental tools for stable genomic integration of transgenes. The piggyBac (PB) transposon from Trichoplusia ni presents a number of benefits over classic viral or BAC transgenesis: ease of application, simple integration-site mapping, and the unique capacity for traceless excision. Moreover, their large capacity permits the consolidation of multiple transgene components in a single vector system. In this chapter, we outline the features of a panel of “All-in-One” PB transposons designed for drug-inducible gene expression and provide guidelines to establish and validate populations or clones of transgenic hiPSCs.</abstract><cop>New York, NY</cop><pub>Springer New York</pub><pmid>26025620</pmid><doi>10.1007/7651_2015_251</doi><tpages>21</tpages></addata></record> |
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subjects | Cell Culture Techniques - methods Cell Separation - methods Cell Tracking - methods Cells, Cultured Cellular Reprogramming Cellular Reprogramming Techniques - methods Clone Cells - cytology DNA Transposable Elements - genetics Doxycycline - pharmacology Doxycycline regulated Fibroblasts - cytology Gene expression Gene Expression - drug effects Gene Expression - genetics Genes, Reporter Genetic Vectors - genetics Green Fluorescent Proteins - genetics Human induced pluripotent stem cell (hiPSC) Humans Induced Pluripotent Stem Cells - cytology Induced Pluripotent Stem Cells - metabolism Luciferases - genetics Luminescent Proteins - genetics Neomycin - pharmacology Puromycin - pharmacology Red Fluorescent Protein Reprogramming Stable transgenesis Transgenes - genetics Transposon |
title | Inducible Transgene Expression in Human iPS Cells Using Versatile All-in-One piggyBac Transposons |
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