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Genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells

In model organisms, classical genetic screening via random mutagenesis provides key insights into the molecular bases of genetic interactions, helping defining synthetic-lethality, synthetic-viability and drug-resistance mechanisms. The limited genetic tractability of diploid mammalian cells, howeve...

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Autores principales: Forment, Josep V., Herzog, Mareike, Coates, Julia, Konopka, Tomasz, Gapp, Bianca V., Nijman, Sebastian M., Adams, David J., Keane, Thomas M., Jackson, Stephen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5164930/
https://www.ncbi.nlm.nih.gov/pubmed/27820796
http://dx.doi.org/10.1038/nchembio.2226
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author Forment, Josep V.
Herzog, Mareike
Coates, Julia
Konopka, Tomasz
Gapp, Bianca V.
Nijman, Sebastian M.
Adams, David J.
Keane, Thomas M.
Jackson, Stephen P.
author_facet Forment, Josep V.
Herzog, Mareike
Coates, Julia
Konopka, Tomasz
Gapp, Bianca V.
Nijman, Sebastian M.
Adams, David J.
Keane, Thomas M.
Jackson, Stephen P.
author_sort Forment, Josep V.
collection PubMed
description In model organisms, classical genetic screening via random mutagenesis provides key insights into the molecular bases of genetic interactions, helping defining synthetic-lethality, synthetic-viability and drug-resistance mechanisms. The limited genetic tractability of diploid mammalian cells, however, precludes this approach. Here, we demonstrate the feasibility of classical genetic screening in mammalian systems by using haploid cells, chemical mutagenesis and next-generation sequencing, providing a new tool to explore mammalian genetic interactions.
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spelling pubmed-51649302017-04-30 Genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells Forment, Josep V. Herzog, Mareike Coates, Julia Konopka, Tomasz Gapp, Bianca V. Nijman, Sebastian M. Adams, David J. Keane, Thomas M. Jackson, Stephen P. Nat Chem Biol Article In model organisms, classical genetic screening via random mutagenesis provides key insights into the molecular bases of genetic interactions, helping defining synthetic-lethality, synthetic-viability and drug-resistance mechanisms. The limited genetic tractability of diploid mammalian cells, however, precludes this approach. Here, we demonstrate the feasibility of classical genetic screening in mammalian systems by using haploid cells, chemical mutagenesis and next-generation sequencing, providing a new tool to explore mammalian genetic interactions. 2016-10-31 2017-01 /pmc/articles/PMC5164930/ /pubmed/27820796 http://dx.doi.org/10.1038/nchembio.2226 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Forment, Josep V.
Herzog, Mareike
Coates, Julia
Konopka, Tomasz
Gapp, Bianca V.
Nijman, Sebastian M.
Adams, David J.
Keane, Thomas M.
Jackson, Stephen P.
Genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells
title Genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells
title_full Genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells
title_fullStr Genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells
title_full_unstemmed Genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells
title_short Genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells
title_sort genome-wide genetic screening with chemically-mutagenized haploid embryonic stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5164930/
https://www.ncbi.nlm.nih.gov/pubmed/27820796
http://dx.doi.org/10.1038/nchembio.2226
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