CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells

Base editors can inactivate splice sites or introduce stop codons into a gene sequence. Here the authors present SpliceR to design, rank, and test sgRNAs for efficient gene disruption in T cells.

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Autores principales: Mitchell G. Kluesner, Walker S. Lahr, Cara-lin Lonetree, Branden A. Smeester, Xiaohong Qiu, Nicholas J. Slipek, Patricia N. Claudio Vázquez, Samuel P. Pitzen, Emily J. Pomeroy, Madison J. Vignes, Samantha C. Lee, Samuel P. Bingea, Aneesha A. Andrew, Beau R. Webber, Branden S. Moriarity
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/66661828f7814bdf8c8c049d29a4b13b
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spelling oai:doaj.org-article:66661828f7814bdf8c8c049d29a4b13b2021-12-02T13:39:33ZCRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells10.1038/s41467-021-22009-22041-1723https://doaj.org/article/66661828f7814bdf8c8c049d29a4b13b2021-04-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-22009-2https://doaj.org/toc/2041-1723Base editors can inactivate splice sites or introduce stop codons into a gene sequence. Here the authors present SpliceR to design, rank, and test sgRNAs for efficient gene disruption in T cells.Mitchell G. KluesnerWalker S. LahrCara-lin LonetreeBranden A. SmeesterXiaohong QiuNicholas J. SlipekPatricia N. Claudio VázquezSamuel P. PitzenEmily J. PomeroyMadison J. VignesSamantha C. LeeSamuel P. BingeaAneesha A. AndrewBeau R. WebberBranden S. MoriarityNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Mitchell G. Kluesner
Walker S. Lahr
Cara-lin Lonetree
Branden A. Smeester
Xiaohong Qiu
Nicholas J. Slipek
Patricia N. Claudio Vázquez
Samuel P. Pitzen
Emily J. Pomeroy
Madison J. Vignes
Samantha C. Lee
Samuel P. Bingea
Aneesha A. Andrew
Beau R. Webber
Branden S. Moriarity
CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells
description Base editors can inactivate splice sites or introduce stop codons into a gene sequence. Here the authors present SpliceR to design, rank, and test sgRNAs for efficient gene disruption in T cells.
format article
author Mitchell G. Kluesner
Walker S. Lahr
Cara-lin Lonetree
Branden A. Smeester
Xiaohong Qiu
Nicholas J. Slipek
Patricia N. Claudio Vázquez
Samuel P. Pitzen
Emily J. Pomeroy
Madison J. Vignes
Samantha C. Lee
Samuel P. Bingea
Aneesha A. Andrew
Beau R. Webber
Branden S. Moriarity
author_facet Mitchell G. Kluesner
Walker S. Lahr
Cara-lin Lonetree
Branden A. Smeester
Xiaohong Qiu
Nicholas J. Slipek
Patricia N. Claudio Vázquez
Samuel P. Pitzen
Emily J. Pomeroy
Madison J. Vignes
Samantha C. Lee
Samuel P. Bingea
Aneesha A. Andrew
Beau R. Webber
Branden S. Moriarity
author_sort Mitchell G. Kluesner
title CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells
title_short CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells
title_full CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells
title_fullStr CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells
title_full_unstemmed CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells
title_sort crispr-cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/66661828f7814bdf8c8c049d29a4b13b
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