Alternative Splicing of PTC7 in Saccharomyces cerevisiae Determines Protein Localization

Author:

Juneau Kara1,Nislow Corey2,Davis Ronald W1

Affiliation:

1. Stanford Genome Technology Center, Department of Biochemistry, Stanford University School of Medicine, Palo Alto, California 94304 and

2. Banting and Best Department of Medical Research, Department of Molecular Genetics, Donnelley Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario M5S 3E1, Canada

Abstract

Abstract It is well established that higher eukaryotes use alternative splicing to increase proteome complexity. In contrast, Saccharomyces cerevisiae, a single-cell eukaryote, conducts predominantly regulated splicing through retention of nonfunctional introns. In this article we describe our discovery of a functional intron in the PTC7 (YHR076W) gene that can be alternatively spliced to create two mRNAs that code for distinct proteins. These two proteins localize to different cellular compartments and have distinct cellular roles. The protein translated from the spliced mRNA localizes to the mitochondria and its expression is carbon-source dependent. In comparison, the protein translated from the unspliced mRNA contains a transmembrane domain, localizes to the nuclear envelope, and mediates the toxic effects of Latrunculin A exposure. In conclusion, we identified a definitive example of functional alternative splicing in S. cerevisiae that confers a measurable fitness benefit.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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