Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions

Human pluripotent stem cells (hPSCs) with knockout or mutant alleles can be generated using custom-engineered nucleases. Transcription activator-like effector nucleases (TALENs) and clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 nucleases are the most commonly employed techn...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cell stem cell 2016-01, Vol.18 (1), p.53-65
Hauptverfasser: Hendriks, William T., Warren, Curtis R., Cowan, Chad A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 65
container_issue 1
container_start_page 53
container_title Cell stem cell
container_volume 18
creator Hendriks, William T.
Warren, Curtis R.
Cowan, Chad A.
description Human pluripotent stem cells (hPSCs) with knockout or mutant alleles can be generated using custom-engineered nucleases. Transcription activator-like effector nucleases (TALENs) and clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 nucleases are the most commonly employed technologies for editing hPSC genomes. In this Protocol Review, we provide a brief overview of custom-engineered nucleases in the context of gene editing in hPSCs with a focus on the application of TALENs and CRISPR/Cas9. We will highlight the advantages and disadvantages of each method and discuss theoretical and technical considerations for experimental design. In this Protocol Review, Hendriks et al. provide a brief overview of custom-engineered nucleases for gene editing in hPSCs with a focus on the application of TALENs and CRISPR/Cas9. They highlight the advantages and disadvantages of each method and discuss theoretical and technical considerations for experimental design.
doi_str_mv 10.1016/j.stem.2015.12.002
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4709030</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1934590915005470</els_id><sourcerecordid>1760891710</sourcerecordid><originalsourceid>FETCH-LOGICAL-c455t-1ebef2177706cf7ea3eed5da889718717b99406a9aebdb51f00f8dbef2ab10e53</originalsourceid><addsrcrecordid>eNp9UcFu1DAQtRCIlsIPcEA-cmjCOBvHMUJI1aq0SJWotHC2HHvSepXYwXYq8fd4taWCCydbM--9eTOPkLcMagas-7CvU8a5boDxmjU1QPOMnLJe8EoKIZ6Xv9y0FZcgT8irlPYAXDAQL8lJ04m24LpTsrtCH2akl9Zl5--o8_R6nbWnt9Ma3RIy-kx3ZQzd4jSlj_RiWWLQ5h7TOb11edSlek61t3QXpjW74NNr8qKUE755fM_Ijy-X37fX1c23q6_bi5vKtJzniuGAY8OKVejMKFBvEC23uu-lKFswMUjZQqelxsEOnI0AY28PHD0wQL45I5-Puss6zGhNsRr1pJboZh1_qaCd-rfj3b26Cw-qFSBhA0Xg_aNADD9XTFnNLpmyp_YY1qSY6KCXrBytQJsj1MSQUsTxaQwDdUhD7dUhDXVIQ7FGlTQK6d3fBp8of85fAJ-OACxnenAYVTIOvUHrIpqsbHD_0_8NkAadfA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1760891710</pqid></control><display><type>article</type><title>Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions</title><source>MEDLINE</source><source>Cell Press Free Archives</source><source>Elsevier ScienceDirect Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Hendriks, William T. ; Warren, Curtis R. ; Cowan, Chad A.</creator><creatorcontrib>Hendriks, William T. ; Warren, Curtis R. ; Cowan, Chad A.</creatorcontrib><description>Human pluripotent stem cells (hPSCs) with knockout or mutant alleles can be generated using custom-engineered nucleases. Transcription activator-like effector nucleases (TALENs) and clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 nucleases are the most commonly employed technologies for editing hPSC genomes. In this Protocol Review, we provide a brief overview of custom-engineered nucleases in the context of gene editing in hPSCs with a focus on the application of TALENs and CRISPR/Cas9. We will highlight the advantages and disadvantages of each method and discuss theoretical and technical considerations for experimental design. In this Protocol Review, Hendriks et al. provide a brief overview of custom-engineered nucleases for gene editing in hPSCs with a focus on the application of TALENs and CRISPR/Cas9. They highlight the advantages and disadvantages of each method and discuss theoretical and technical considerations for experimental design.</description><identifier>ISSN: 1934-5909</identifier><identifier>EISSN: 1875-9777</identifier><identifier>DOI: 10.1016/j.stem.2015.12.002</identifier><identifier>PMID: 26748756</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alleles ; CRISPR-Cas Systems ; Deoxyribonucleases - genetics ; Deoxyribonucleases - metabolism ; DNA - analysis ; Genetic Techniques ; Genetic Vectors ; Genome, Human ; Genotype ; Humans ; Mutation ; Pluripotent Stem Cells - cytology ; Point Mutation ; Sequence Homology, Nucleic Acid</subject><ispartof>Cell stem cell, 2016-01, Vol.18 (1), p.53-65</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-1ebef2177706cf7ea3eed5da889718717b99406a9aebdb51f00f8dbef2ab10e53</citedby><cites>FETCH-LOGICAL-c455t-1ebef2177706cf7ea3eed5da889718717b99406a9aebdb51f00f8dbef2ab10e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1934590915005470$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26748756$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hendriks, William T.</creatorcontrib><creatorcontrib>Warren, Curtis R.</creatorcontrib><creatorcontrib>Cowan, Chad A.</creatorcontrib><title>Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions</title><title>Cell stem cell</title><addtitle>Cell Stem Cell</addtitle><description>Human pluripotent stem cells (hPSCs) with knockout or mutant alleles can be generated using custom-engineered nucleases. Transcription activator-like effector nucleases (TALENs) and clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 nucleases are the most commonly employed technologies for editing hPSC genomes. In this Protocol Review, we provide a brief overview of custom-engineered nucleases in the context of gene editing in hPSCs with a focus on the application of TALENs and CRISPR/Cas9. We will highlight the advantages and disadvantages of each method and discuss theoretical and technical considerations for experimental design. In this Protocol Review, Hendriks et al. provide a brief overview of custom-engineered nucleases for gene editing in hPSCs with a focus on the application of TALENs and CRISPR/Cas9. They highlight the advantages and disadvantages of each method and discuss theoretical and technical considerations for experimental design.</description><subject>Alleles</subject><subject>CRISPR-Cas Systems</subject><subject>Deoxyribonucleases - genetics</subject><subject>Deoxyribonucleases - metabolism</subject><subject>DNA - analysis</subject><subject>Genetic Techniques</subject><subject>Genetic Vectors</subject><subject>Genome, Human</subject><subject>Genotype</subject><subject>Humans</subject><subject>Mutation</subject><subject>Pluripotent Stem Cells - cytology</subject><subject>Point Mutation</subject><subject>Sequence Homology, Nucleic Acid</subject><issn>1934-5909</issn><issn>1875-9777</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UcFu1DAQtRCIlsIPcEA-cmjCOBvHMUJI1aq0SJWotHC2HHvSepXYwXYq8fd4taWCCydbM--9eTOPkLcMagas-7CvU8a5boDxmjU1QPOMnLJe8EoKIZ6Xv9y0FZcgT8irlPYAXDAQL8lJ04m24LpTsrtCH2akl9Zl5--o8_R6nbWnt9Ma3RIy-kx3ZQzd4jSlj_RiWWLQ5h7TOb11edSlek61t3QXpjW74NNr8qKUE755fM_Ijy-X37fX1c23q6_bi5vKtJzniuGAY8OKVejMKFBvEC23uu-lKFswMUjZQqelxsEOnI0AY28PHD0wQL45I5-Puss6zGhNsRr1pJboZh1_qaCd-rfj3b26Cw-qFSBhA0Xg_aNADD9XTFnNLpmyp_YY1qSY6KCXrBytQJsj1MSQUsTxaQwDdUhD7dUhDXVIQ7FGlTQK6d3fBp8of85fAJ-OACxnenAYVTIOvUHrIpqsbHD_0_8NkAadfA</recordid><startdate>20160107</startdate><enddate>20160107</enddate><creator>Hendriks, William T.</creator><creator>Warren, Curtis R.</creator><creator>Cowan, Chad A.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160107</creationdate><title>Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions</title><author>Hendriks, William T. ; Warren, Curtis R. ; Cowan, Chad A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-1ebef2177706cf7ea3eed5da889718717b99406a9aebdb51f00f8dbef2ab10e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Alleles</topic><topic>CRISPR-Cas Systems</topic><topic>Deoxyribonucleases - genetics</topic><topic>Deoxyribonucleases - metabolism</topic><topic>DNA - analysis</topic><topic>Genetic Techniques</topic><topic>Genetic Vectors</topic><topic>Genome, Human</topic><topic>Genotype</topic><topic>Humans</topic><topic>Mutation</topic><topic>Pluripotent Stem Cells - cytology</topic><topic>Point Mutation</topic><topic>Sequence Homology, Nucleic Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hendriks, William T.</creatorcontrib><creatorcontrib>Warren, Curtis R.</creatorcontrib><creatorcontrib>Cowan, Chad A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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 stem cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hendriks, William T.</au><au>Warren, Curtis R.</au><au>Cowan, Chad A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions</atitle><jtitle>Cell stem cell</jtitle><addtitle>Cell Stem Cell</addtitle><date>2016-01-07</date><risdate>2016</risdate><volume>18</volume><issue>1</issue><spage>53</spage><epage>65</epage><pages>53-65</pages><issn>1934-5909</issn><eissn>1875-9777</eissn><abstract>Human pluripotent stem cells (hPSCs) with knockout or mutant alleles can be generated using custom-engineered nucleases. Transcription activator-like effector nucleases (TALENs) and clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 nucleases are the most commonly employed technologies for editing hPSC genomes. In this Protocol Review, we provide a brief overview of custom-engineered nucleases in the context of gene editing in hPSCs with a focus on the application of TALENs and CRISPR/Cas9. We will highlight the advantages and disadvantages of each method and discuss theoretical and technical considerations for experimental design. In this Protocol Review, Hendriks et al. provide a brief overview of custom-engineered nucleases for gene editing in hPSCs with a focus on the application of TALENs and CRISPR/Cas9. They highlight the advantages and disadvantages of each method and discuss theoretical and technical considerations for experimental design.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26748756</pmid><doi>10.1016/j.stem.2015.12.002</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1934-5909
ispartof Cell stem cell, 2016-01, Vol.18 (1), p.53-65
issn 1934-5909
1875-9777
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4709030
source MEDLINE; Cell Press Free Archives; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Alleles
CRISPR-Cas Systems
Deoxyribonucleases - genetics
Deoxyribonucleases - metabolism
DNA - analysis
Genetic Techniques
Genetic Vectors
Genome, Human
Genotype
Humans
Mutation
Pluripotent Stem Cells - cytology
Point Mutation
Sequence Homology, Nucleic Acid
title Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T08%3A48%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genome%20Editing%20in%20Human%20Pluripotent%20Stem%20Cells:%20Approaches,%20Pitfalls,%20and%20Solutions&rft.jtitle=Cell%20stem%20cell&rft.au=Hendriks,%20William%C2%A0T.&rft.date=2016-01-07&rft.volume=18&rft.issue=1&rft.spage=53&rft.epage=65&rft.pages=53-65&rft.issn=1934-5909&rft.eissn=1875-9777&rft_id=info:doi/10.1016/j.stem.2015.12.002&rft_dat=%3Cproquest_pubme%3E1760891710%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1760891710&rft_id=info:pmid/26748756&rft_els_id=S1934590915005470&rfr_iscdi=true