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...
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Veröffentlicht in: | Cell stem cell 2016-01, Vol.18 (1), p.53-65 |
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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 |
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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.
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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 |
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