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Transgenic mice with defined combinations of drug-inducible reprogramming factors
Proviruses carrying drug-inducible Oct4, Sox2, Klf4 and c-Myc used to derive 'primary' induced pluripotent stem (iPS) cells were segregated through germline transmission, generating mice and cells carrying subsets of the reprogramming factors. Drug treatment produced 'secondary'...
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Published in: | Nature biotechnology 2009-02, Vol.27 (2), p.169-171 |
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container_end_page | 171 |
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container_title | Nature biotechnology |
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creator | Jaenisch, Rudolf Markoulaki, Styliani Hanna, Jacob Beard, Caroline Carey, Bryce W Cheng, Albert W Lengner, Christopher J Dausman, Jessica A Fu, Dongdong Gao, Qing Wu, Su Cassady, John P |
description | Proviruses carrying drug-inducible Oct4, Sox2, Klf4 and c-Myc used to derive 'primary' induced pluripotent stem (iPS) cells were segregated through germline transmission, generating mice and cells carrying subsets of the reprogramming factors. Drug treatment produced 'secondary' iPS cells only when the missing factor was introduced. This approach creates a defined system for studying reprogramming mechanisms and allows screening of genetically homogeneous cells for compounds that can replace any transcription factor required for iPS cell derivation. |
doi_str_mv | 10.1038/nbt.1520 |
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Drug treatment produced 'secondary' iPS cells only when the missing factor was introduced. This approach creates a defined system for studying reprogramming mechanisms and allows screening of genetically homogeneous cells for compounds that can replace any transcription factor required for iPS cell derivation.</description><identifier>ISSN: 1087-0156</identifier><identifier>EISSN: 1546-1696</identifier><identifier>DOI: 10.1038/nbt.1520</identifier><identifier>PMID: 19151700</identifier><identifier>CODEN: NABIF9</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>Agriculture ; Animals ; Bioinformatics ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedical Engineering/Biotechnology ; Biomedicine ; Biotechnology ; brief-communication ; Cell Differentiation - drug effects ; Cell Differentiation - genetics ; Cells, Cultured ; Chimera - genetics ; Chimera - metabolism ; DNA binding proteins ; Doxycycline - pharmacology ; Female ; Fibroblasts - metabolism ; Fundamental and applied biological sciences. Psychology ; Genetic aspects ; Genetic Techniques ; Genetically modified mice ; Genetics ; Health aspects ; Health. Pharmaceutical industry ; Industrial applications and implications. Economical aspects ; Kruppel-Like Transcription Factors - genetics ; Kruppel-Like Transcription Factors - metabolism ; Life Sciences ; Male ; Mice ; Mice, Transgenic ; Miscellaneous ; Octamer Transcription Factor-3 - genetics ; Octamer Transcription Factor-3 - metabolism ; Physiological aspects ; Pluripotent Stem Cells ; Proto-Oncogene Proteins c-myc - genetics ; Proto-Oncogene Proteins c-myc - metabolism ; Proviruses - genetics ; Proviruses - metabolism ; Rodents ; SOXB1 Transcription Factors - genetics ; SOXB1 Transcription Factors - metabolism ; Stem cells ; Transcription Factors - drug effects ; Transcription Factors - genetics ; Transgenic animals</subject><ispartof>Nature biotechnology, 2009-02, Vol.27 (2), p.169-171</ispartof><rights>Springer Nature America, Inc. 2009</rights><rights>2009 INIST-CNRS</rights><rights>COPYRIGHT 2009 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Feb 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c659t-6779c54fa382534fdf49f8ce66df1e98f10b7e70d84326efa71f3002eef3f5df3</citedby><cites>FETCH-LOGICAL-c659t-6779c54fa382534fdf49f8ce66df1e98f10b7e70d84326efa71f3002eef3f5df3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,2727,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21267386$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19151700$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jaenisch, Rudolf</creatorcontrib><creatorcontrib>Markoulaki, Styliani</creatorcontrib><creatorcontrib>Hanna, Jacob</creatorcontrib><creatorcontrib>Beard, Caroline</creatorcontrib><creatorcontrib>Carey, Bryce W</creatorcontrib><creatorcontrib>Cheng, Albert W</creatorcontrib><creatorcontrib>Lengner, Christopher J</creatorcontrib><creatorcontrib>Dausman, Jessica A</creatorcontrib><creatorcontrib>Fu, Dongdong</creatorcontrib><creatorcontrib>Gao, Qing</creatorcontrib><creatorcontrib>Wu, Su</creatorcontrib><creatorcontrib>Cassady, John P</creatorcontrib><title>Transgenic mice with defined combinations of drug-inducible reprogramming factors</title><title>Nature biotechnology</title><addtitle>Nat Biotechnol</addtitle><addtitle>Nat Biotechnol</addtitle><description>Proviruses carrying drug-inducible Oct4, Sox2, Klf4 and c-Myc used to derive 'primary' induced pluripotent stem (iPS) cells were segregated through germline transmission, generating mice and cells carrying subsets of the reprogramming factors. Drug treatment produced 'secondary' iPS cells only when the missing factor was introduced. This approach creates a defined system for studying reprogramming mechanisms and allows screening of genetically homogeneous cells for compounds that can replace any transcription factor required for iPS cell derivation.</description><subject>Agriculture</subject><subject>Animals</subject><subject>Bioinformatics</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering/Biotechnology</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>brief-communication</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - genetics</subject><subject>Cells, Cultured</subject><subject>Chimera - genetics</subject><subject>Chimera - metabolism</subject><subject>DNA binding proteins</subject><subject>Doxycycline - pharmacology</subject><subject>Female</subject><subject>Fibroblasts - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic aspects</subject><subject>Genetic Techniques</subject><subject>Genetically modified mice</subject><subject>Genetics</subject><subject>Health aspects</subject><subject>Health. Pharmaceutical industry</subject><subject>Industrial applications and implications. 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subjects | Agriculture Animals Bioinformatics Biological and medical sciences Biomedical and Life Sciences Biomedical Engineering/Biotechnology Biomedicine Biotechnology brief-communication Cell Differentiation - drug effects Cell Differentiation - genetics Cells, Cultured Chimera - genetics Chimera - metabolism DNA binding proteins Doxycycline - pharmacology Female Fibroblasts - metabolism Fundamental and applied biological sciences. Psychology Genetic aspects Genetic Techniques Genetically modified mice Genetics Health aspects Health. Pharmaceutical industry Industrial applications and implications. Economical aspects Kruppel-Like Transcription Factors - genetics Kruppel-Like Transcription Factors - metabolism Life Sciences Male Mice Mice, Transgenic Miscellaneous Octamer Transcription Factor-3 - genetics Octamer Transcription Factor-3 - metabolism Physiological aspects Pluripotent Stem Cells Proto-Oncogene Proteins c-myc - genetics Proto-Oncogene Proteins c-myc - metabolism Proviruses - genetics Proviruses - metabolism Rodents SOXB1 Transcription Factors - genetics SOXB1 Transcription Factors - metabolism Stem cells Transcription Factors - drug effects Transcription Factors - genetics Transgenic animals |
title | Transgenic mice with defined combinations of drug-inducible reprogramming factors |
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