Gene essentiality and synthetic lethality in haploid human cells

Vincent A. Blomen(The Netherlands Cancer Institute), Peter Májek(Austrian Academy of Sciences), Lucas T. Jae(The Netherlands Cancer Institute), Johannes W. Bigenzahn(Austrian Academy of Sciences), Joppe Nieuwenhuis(The Netherlands Cancer Institute), Jacqueline Staring(The Netherlands Cancer Institute), Roberto Sacco(Austrian Academy of Sciences), Ferdy R. van Diemen(The Netherlands Cancer Institute), Nadine Olk(Austrian Academy of Sciences), Alexey Stukalov(Austrian Academy of Sciences), Caleb Marceau(Stanford University), Hans Janßen(The Netherlands Cancer Institute), Jan E. Carette(Stanford University), Keiryn L. Bennett(Austrian Academy of Sciences), Jacques Colinge(Austrian Academy of Sciences), Giulio Superti‐Furga(Austrian Academy of Sciences), Thijn R. Brummelkamp(Austrian Academy of Sciences)
Science
October 15, 2015
Cited by 945

Abstract

Although the genes essential for life have been identified in less complex model organisms, their elucidation in human cells has been hindered by technical barriers. We used extensive mutagenesis in haploid human cells to identify approximately 2000 genes required for optimal fitness under culture conditions. To study the principles of genetic interactions in human cells, we created a synthetic lethality network focused on the secretory pathway based exclusively on mutations. This revealed a genetic cross-talk governing Golgi homeostasis, an additional subunit of the human oligosaccharyltransferase complex, and a phosphatidylinositol 4-kinase β adaptor hijacked by viruses. The synthetic lethality map parallels observations made in yeast and projects a route forward to reveal genetic networks in diverse aspects of human cell biology.


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