Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant

Manipulating DNA repair pathways can be used to improve the outcomes of CRISPR-based genome editing. Here the authors derive an enhanced RAD18 variant that suppresses 53BP1 recruitment to DNA double-strand breaks to enhance homology-mediated repair.

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Autores principales: Tarun S. Nambiar, Pierre Billon, Giacomo Diedenhofen, Samuel B. Hayward, Angelo Taglialatela, Kunheng Cai, Jen-Wei Huang, Giuseppe Leuzzi, Raquel Cuella-Martin, Andrew Palacios, Anuj Gupta, Dieter Egli, Alberto Ciccia
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Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/f4d885e322c6447198d8c7f4fa611f33
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spelling oai:doaj.org-article:f4d885e322c6447198d8c7f4fa611f332021-12-02T15:35:57ZStimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant10.1038/s41467-019-11105-z2041-1723https://doaj.org/article/f4d885e322c6447198d8c7f4fa611f332019-07-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-11105-zhttps://doaj.org/toc/2041-1723Manipulating DNA repair pathways can be used to improve the outcomes of CRISPR-based genome editing. Here the authors derive an enhanced RAD18 variant that suppresses 53BP1 recruitment to DNA double-strand breaks to enhance homology-mediated repair.Tarun S. NambiarPierre BillonGiacomo DiedenhofenSamuel B. HaywardAngelo TaglialatelaKunheng CaiJen-Wei HuangGiuseppe LeuzziRaquel Cuella-MartinAndrew PalaciosAnuj GuptaDieter EgliAlberto CicciaNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Tarun S. Nambiar
Pierre Billon
Giacomo Diedenhofen
Samuel B. Hayward
Angelo Taglialatela
Kunheng Cai
Jen-Wei Huang
Giuseppe Leuzzi
Raquel Cuella-Martin
Andrew Palacios
Anuj Gupta
Dieter Egli
Alberto Ciccia
Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant
description Manipulating DNA repair pathways can be used to improve the outcomes of CRISPR-based genome editing. Here the authors derive an enhanced RAD18 variant that suppresses 53BP1 recruitment to DNA double-strand breaks to enhance homology-mediated repair.
format article
author Tarun S. Nambiar
Pierre Billon
Giacomo Diedenhofen
Samuel B. Hayward
Angelo Taglialatela
Kunheng Cai
Jen-Wei Huang
Giuseppe Leuzzi
Raquel Cuella-Martin
Andrew Palacios
Anuj Gupta
Dieter Egli
Alberto Ciccia
author_facet Tarun S. Nambiar
Pierre Billon
Giacomo Diedenhofen
Samuel B. Hayward
Angelo Taglialatela
Kunheng Cai
Jen-Wei Huang
Giuseppe Leuzzi
Raquel Cuella-Martin
Andrew Palacios
Anuj Gupta
Dieter Egli
Alberto Ciccia
author_sort Tarun S. Nambiar
title Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant
title_short Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant
title_full Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant
title_fullStr Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant
title_full_unstemmed Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant
title_sort stimulation of crispr-mediated homology-directed repair by an engineered rad18 variant
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/f4d885e322c6447198d8c7f4fa611f33
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