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Article
Nature 423, 720-725 (12 June 2003) | doi:10.1038/nature01692; Received 25 February 2003; Accepted 6 May 2003; Published online 25 May 2003
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Functional proteomic identification of DNA replication proteins by induced proteolysis in vivo
Masato Kanemaki1, Alberto Sanchez-Diaz1, Agnieszka Gambus & Karim Labib
- Cancer Research UK, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Wilmslow Road, Manchester, M20 4BX, UK
- These authors contributed equally to this work
Correspondence to: Karim Labib Correspondence and requests for materials should be addressed to K.L. (Email: klabib@picr.man.ac.uk).
Abstract
Evolutionarily diverse eukaryotic cells share many conserved proteins of unknown function. Some are essential for cell viability1, 2, emphasising their importance for fundamental processes of cell biology but complicating their analysis. We have developed an approach to the large-scale characterization of such proteins, based on conditional and rapid degradation of the target protein in vivo, so that the immediate consequences of bulk protein depletion can be examined3. Budding yeast strains have been constructed in which essential proteins of unknown function have been fused to a 'heat-inducible-degron' cassette that targets the protein for proteolysis at 37 °C (ref. 4). By screening the collection for defects in cell-cycle progression, here we identify three DNA replication factors that interact with each other and that have uncharacterized homologues in human cells. We have used the degron strains to show that these proteins are required for the establishment and normal progression of DNA replication forks. The degron collection could also be used to identify other, essential, proteins with roles in many other processes of eukaryotic cell biology.
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