Sbp1p Affects Translational Repression and Decapping in Saccharomyces cerevisiae

Abstract

The relationship between translation and mRNA turnover is critical to the regulation of gene expression. One major pathway for mRNA turnover occurs by deadenylation, which leads to decapping and subsequent 5′-to-3′ degradation of the body of the mRNA. Prior to mRNA decapping, a transcript exits translation and enters P bodies to become a potential decapping substrate. To understand the transition from translation to decapping, it is important to identify the factors involved in this process. In this work, we identify Sbp1p (formerly known as Ssb1p), an abundant RNA binding protein, as a high-copy-number suppressor of a conditional allele in the decapping enzyme. Sbp1p overexpression restores normal decay rates in decapping-defective strains and increases P-body size and number. In addition, Sbp1p promotes translational repression of mRNA during glucose deprivation. Moreover, P-body formation is reduced in strains lacking Sbp1p. Sbp1p acts in conjunction with Dhh1p, as it is required for translational repression and P-body formation in pat1Δ strains under these conditions. These results identify Sbp1p as a new protein that functions in the transition of mRNAs from translation to an mRNP complex destined for decapping.

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Sbp1p Affects Translational Repression and Decapping in Saccharomyces cerevisiae

We thank Denise Muhlrad, Debrah Thompson, Carolyn Decker, Tracy Nissan, and Scott Barbee for thoughtful advice and critical reading of the manuscript, as well as the members of Roy Parker's laboratory for useful discussion. We also thank Denise Muhlrad for construction of the SBP1-2μm plasmids and Bettsy Valencia for help with strain maintenance.

This work was supported by HHMI.