TY - JOUR
T1 - A novel single-cell screening platform reveals proteome plasticity during yeast stress responses
AU - Breker, Michal
AU - Gymrek, Melissa
AU - Schuldiner, Maya
N1 - Minerva Minna James Heineman Stiftung; European Research Council StG [260395]; Israeli Science Foundation (ISF) [1995/08]; Human Frontiers Science Program [CDA0006/2008-C]; MIT International Science and Technology Initiatives (MISTI)This work was funded by the Minerva Minna James Heineman Stiftung grant and by a European Research Council StG (260395). The robotic setup was purchased through the generous support of the Israeli Science Foundation (ISF) Legacy Heritage fund (grant No. 1995/08) and the Human Frontiers Science Program (CDA0006/2008-C) as well as through the generous donation of Mr. James Nathan, Beverly Hills, CA, and the Estate of Lela London. M. Gymrek was supported by the MIT International Science and Technology Initiatives (MISTI). The authors declare that they have no competing financial interests.
PY - 2013/3
Y1 - 2013/3
N2 - 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).
AB - 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).
UR - http://www.scopus.com/inward/record.url?scp=84876305060&partnerID=8YFLogxK
U2 - 10.1083/jcb.201301120
DO - 10.1083/jcb.201301120
M3 - مقالة
C2 - 23509072
SN - 0021-9525
VL - 200
SP - 839
EP - 850
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 6
ER -