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Traffic. 2011 Nov;12(11):1592-603. doi: 10.1111/j.1600-0854.2011.01252.x. Epub 2011 Aug 18.

An overexpression screen in Saccharomyces cerevisiae identifies novel genes that affect endocytic protein trafficking.

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  • 1Department of Biology/Chemistry, Biochemistry section, University of Osnabrück, Osnabrück 49076, Germany.


A large number of proteins involved in the biogenesis of yeast endosomes and vacuoles have been identified based on screens that scored for inactivation of proteins. Such screens may, however, miss important regulators of the pathway. Here, we present a visual screen in which we examined the effects on vacuole morphology if any of the 6153 yeast open reading frames was overexpressed. Using a progressive screening procedure, we could identify a total of 53 genes. Among the most striking endosomal proteins are the CORVET/HOPS subunits Vps3, Vps18 and Vps39 and the putative tethering inhibitor Ivy1. Furthermore, six endosomal sorting complex related to transport (ESCRT) proteins led to altered vacuole morphology if overproduced. Among the novel proteins, we identify Yer128w as an endosomal protein that interacts with the AAA-ATPase Vps4, and therefore named it Vfa1 (Vps Four-Associated 1). We present evidence on the possible role of these novel proteins in trafficking to the vacuole. Our data provide novel insights into the regulation of protein trafficking.

© 2011 John Wiley & Sons A/S.

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