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Fluorescence-Based Phenotypic Selection Allows Forward Genetic Screens in Haploid Human Cells

The isolation of haploid cell lines has recently allowed the power of forward genetic screens to be applied to mammalian cells. The interest in applying this powerful genetic approach to a mammalian system is only tempered by the limited utility of these screens, if confined to lethal phenotypes. He...

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Detalles Bibliográficos
Autores principales: Duncan, Lidia M., Timms, Richard T., Zavodszky, Eszter, Cano, Florencia, Dougan, Gordon, Randow, Felix, Lehner, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382162/
https://www.ncbi.nlm.nih.gov/pubmed/22745803
http://dx.doi.org/10.1371/journal.pone.0039651
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author Duncan, Lidia M.
Timms, Richard T.
Zavodszky, Eszter
Cano, Florencia
Dougan, Gordon
Randow, Felix
Lehner, Paul J.
author_facet Duncan, Lidia M.
Timms, Richard T.
Zavodszky, Eszter
Cano, Florencia
Dougan, Gordon
Randow, Felix
Lehner, Paul J.
author_sort Duncan, Lidia M.
collection PubMed
description The isolation of haploid cell lines has recently allowed the power of forward genetic screens to be applied to mammalian cells. The interest in applying this powerful genetic approach to a mammalian system is only tempered by the limited utility of these screens, if confined to lethal phenotypes. Here we expand the scope of these approaches beyond live/dead screens and show that selection for a cell surface phenotype via fluorescence-activated cell sorting can identify the key molecules in an intracellular pathway, in this case MHC class I antigen presentation. Non-lethal haploid genetic screens are widely applicable to identify genes involved in essentially any cellular pathway.
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spelling pubmed-33821622012-06-28 Fluorescence-Based Phenotypic Selection Allows Forward Genetic Screens in Haploid Human Cells Duncan, Lidia M. Timms, Richard T. Zavodszky, Eszter Cano, Florencia Dougan, Gordon Randow, Felix Lehner, Paul J. PLoS One Research Article The isolation of haploid cell lines has recently allowed the power of forward genetic screens to be applied to mammalian cells. The interest in applying this powerful genetic approach to a mammalian system is only tempered by the limited utility of these screens, if confined to lethal phenotypes. Here we expand the scope of these approaches beyond live/dead screens and show that selection for a cell surface phenotype via fluorescence-activated cell sorting can identify the key molecules in an intracellular pathway, in this case MHC class I antigen presentation. Non-lethal haploid genetic screens are widely applicable to identify genes involved in essentially any cellular pathway. Public Library of Science 2012-06-22 /pmc/articles/PMC3382162/ /pubmed/22745803 http://dx.doi.org/10.1371/journal.pone.0039651 Text en Duncan et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Duncan, Lidia M.
Timms, Richard T.
Zavodszky, Eszter
Cano, Florencia
Dougan, Gordon
Randow, Felix
Lehner, Paul J.
Fluorescence-Based Phenotypic Selection Allows Forward Genetic Screens in Haploid Human Cells
title Fluorescence-Based Phenotypic Selection Allows Forward Genetic Screens in Haploid Human Cells
title_full Fluorescence-Based Phenotypic Selection Allows Forward Genetic Screens in Haploid Human Cells
title_fullStr Fluorescence-Based Phenotypic Selection Allows Forward Genetic Screens in Haploid Human Cells
title_full_unstemmed Fluorescence-Based Phenotypic Selection Allows Forward Genetic Screens in Haploid Human Cells
title_short Fluorescence-Based Phenotypic Selection Allows Forward Genetic Screens in Haploid Human Cells
title_sort fluorescence-based phenotypic selection allows forward genetic screens in haploid human cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382162/
https://www.ncbi.nlm.nih.gov/pubmed/22745803
http://dx.doi.org/10.1371/journal.pone.0039651
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