Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors
Multiplexed genome engineering with Cas9 can increase efficiency but also the risk of unintended alterations. Here the authors demonstrate the use of multiplexed base editors on primary T cells with reduced translocation frequency.
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Nature Publishing Group
2019-11-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-019-13007-6 |
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doaj-7b8f9319f4d349b9a42406e609bf1cd42021-05-11T11:59:30ZengNature Publishing GroupNature Communications2041-17232019-11-0110111010.1038/s41467-019-13007-6Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editorsBeau R. Webber0Cara-lin Lonetree1Mitchell G. Kluesner2Matthew J. Johnson3Emily J. Pomeroy4Miechaleen D. Diers5Walker S. Lahr6Garrett M. Draper7Nicholas J. Slipek8Branden A. Smeester9Klaus N. Lovendahl10Amber N. McElroy11Wendy R. Gordon12Mark J. Osborn13Branden S. Moriarity14Department of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Biochemistry, Molecular Biology, and Biophysics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Biochemistry, Molecular Biology, and Biophysics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaDepartment of Pediatrics, University of MinnesotaMultiplexed genome engineering with Cas9 can increase efficiency but also the risk of unintended alterations. Here the authors demonstrate the use of multiplexed base editors on primary T cells with reduced translocation frequency.https://doi.org/10.1038/s41467-019-13007-6 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Beau R. Webber Cara-lin Lonetree Mitchell G. Kluesner Matthew J. Johnson Emily J. Pomeroy Miechaleen D. Diers Walker S. Lahr Garrett M. Draper Nicholas J. Slipek Branden A. Smeester Klaus N. Lovendahl Amber N. McElroy Wendy R. Gordon Mark J. Osborn Branden S. Moriarity |
spellingShingle |
Beau R. Webber Cara-lin Lonetree Mitchell G. Kluesner Matthew J. Johnson Emily J. Pomeroy Miechaleen D. Diers Walker S. Lahr Garrett M. Draper Nicholas J. Slipek Branden A. Smeester Klaus N. Lovendahl Amber N. McElroy Wendy R. Gordon Mark J. Osborn Branden S. Moriarity Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors Nature Communications |
author_facet |
Beau R. Webber Cara-lin Lonetree Mitchell G. Kluesner Matthew J. Johnson Emily J. Pomeroy Miechaleen D. Diers Walker S. Lahr Garrett M. Draper Nicholas J. Slipek Branden A. Smeester Klaus N. Lovendahl Amber N. McElroy Wendy R. Gordon Mark J. Osborn Branden S. Moriarity |
author_sort |
Beau R. Webber |
title |
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors |
title_short |
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors |
title_full |
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors |
title_fullStr |
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors |
title_full_unstemmed |
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors |
title_sort |
highly efficient multiplex human t cell engineering without double-strand breaks using cas9 base editors |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2019-11-01 |
description |
Multiplexed genome engineering with Cas9 can increase efficiency but also the risk of unintended alterations. Here the authors demonstrate the use of multiplexed base editors on primary T cells with reduced translocation frequency. |
url |
https://doi.org/10.1038/s41467-019-13007-6 |
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