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. © 2012 Duncan et al.
CITATION STYLE
Duncan, L. M., Timms, R. T., Zavodszky, E., Cano, F., Dougan, G., Randow, F., & Lehner, P. J. (2012). Fluorescence-based phenotypic selection allows forward genetic screens in haploid human cells. PLoS ONE, 7(6). https://doi.org/10.1371/journal.pone.0039651
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