A novel single-cell screening platform reveals proteome plasticity during yeast stress responses

被引:166
作者
Breker, Michal [1 ]
Gymrek, Melissa [2 ,3 ]
Schuldiner, Maya [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[2] MIT, Harvard MIT Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[3] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
基金
欧洲研究理事会;
关键词
SACCHAROMYCES-CEREVISIAE REVEALS; DYNAMIC PROTEOMICS; NONQUIESCENT CELLS; STATIONARY-PHASE; GENE-EXPRESSION; GLOBAL ANALYSIS; IN-VIVO; LOCALIZATION; PROTEINS; AGGREGATION;
D O I
10.1083/jcb.201301120
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Uncovering the mechanisms underlying robust responses of cells to stress is crucial for our understanding of cellular physiology. Indeed, vast amounts of data have been collected on transcriptional responses in Saccharomyces cerevisiae. However, only a handful of pioneering studies describe the dynamics of proteins in response to external stimuli, despite the fact that regulation of protein levels and localization is an essential part of such responses. Here we characterized unprecedented proteome plasticity by systematically tracking the localization and abundance of 5,330 yeast proteins at single-cell resolution under three different stress conditions (DTT, H2O2, and nitrogen starvation) using the GFP-tagged yeast library. We uncovered a unique "fingerprint" of changes for each stress and elucidated a new response arsenal for adapting to radical environments. These include bet-hedging strategies, organelle rearrangement, and redistribution of protein localizations. All data are available for download through our online database, LOQATE (localization and quantitation atlas of yeast proteome).
引用
收藏
页码:839 / 850
页数:12
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