Exploiting the yeast stress-activated signaling network to inform on stress biology and disease signaling

被引:96
作者
Ho, Yi-Hsuan [1 ]
Gasch, Audrey P. [1 ]
机构
[1] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
关键词
Stress response; Growth control; Transcription; Signal transduction; PROTEIN-KINASE-A; POLYMERASE-III TRANSCRIPTION; MESSENGER-RNA TRANSLATION; RAS/CYCLIC AMP PATHWAY; GENOME-WIDE ANALYSIS; GENE-EXPRESSION; SACCHAROMYCES-CEREVISIAE; RIBOSOMAL-PROTEIN; CELL-CYCLE; NUCLEAR-LOCALIZATION;
D O I
10.1007/s00294-015-0491-0
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Healthy cells utilize intricate systems to monitor their environment and mount robust responses in the event of cellular stress. Whether stress arises from external insults or defects due to mutation and disease, cells must be able to respond precisely to mount the appropriate defenses. Multi-faceted stress responses are generally coupled with arrest of growth and cell-cycle progression, which both limits the transmission of damaged materials and serves to reallocate limited cellular resources toward defense. Therefore, stress defense versus rapid growth represent competing interests in the cell. How eukaryotic cells set the balance between defense versus proliferation, and in particular knowledge of the regulatory networks that control this decision, are poorly understood. In this perspective, we expand upon our recent work inferring the stress-activated signaling network in budding yeast, which captures pathways controlling stress defense and regulators of growth and cell-cycle progression. We highlight similarities between the yeast and mammalian stress responses and explore how stress-activated signaling networks in yeast can inform on signaling defects in human cancers.
引用
收藏
页码:503 / 511
页数:9
相关论文
共 114 条
[1]
Cell cycle checkpoint signaling through the ATM and ATR kinases [J].
Abraham, RT .
GENES & DEVELOPMENT, 2001, 15 (17) :2177-2196
[2]
p53 suppresses carcinoma progression by inhibiting mTOR pathway activation [J].
Akeno, N. ;
Miller, A. L. ;
Ma, X. ;
Wikenheiser-Brokamp, K. A. .
ONCOGENE, 2015, 34 (05) :589-599
[3]
GPD1, WHICH ENCODES GLYCEROL-3-PHOSPHATE DEHYDROGENASE, IS ESSENTIAL FOR GROWTH UNDER OSMOTIC-STRESS IN SACCHAROMYCES-CEREVISIAE, AND ITS EXPRESSION IS REGULATED BY THE HIGH-OSMOLARITY GLYCEROL RESPONSE PATHWAY [J].
ALBERTYN, J ;
HOHMANN, S ;
THEVELEIN, JM ;
PRIOR, BA .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (06) :4135-4144
[4]
Genome-wide analysis of mRNA translation profiles in Saccharomyces cerevisiae [J].
Arava, Y ;
Wang, YL ;
Storey, JD ;
Liu, CL ;
Brown, PO ;
Herschlag, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3889-3894
[5]
The many paths to p38 mitogen-activated protein kinase activation in the immune system [J].
Ashwell, Jonathan D. .
NATURE REVIEWS IMMUNOLOGY, 2006, 6 (07) :532-540
[6]
The TOR signalling pathway controls nuclear localization of nutrient-regulated transcription factors [J].
Beck, T ;
Hall, MN .
NATURE, 1999, 402 (6762) :689-692
[7]
Transcriptional Regulation by p53 [J].
Beckerman, Rachel ;
Prives, Carol .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2010, 2 (08) :a000935
[8]
Osmotic stress causes a G1 cell cycle delay and downregulation of Cln3/Cdc28 activity in Saccharomyces cerevisiae [J].
Belli, G ;
Garí, E ;
Aldea, M ;
Herrero, E .
MOLECULAR MICROBIOLOGY, 2001, 39 (04) :1022-1035
[9]
Stress-activated Genomic Expression Changes Serve a Preparative Role for Impending Stress in Yeast [J].
Berry, David B. ;
Gasch, Audrey P. .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (11) :4580-4587
[10]
Multiple Means to the Same End: The Genetic Basis of Acquired Stress Resistance in Yeast [J].
Berry, David B. ;
Guan, Qiaoning ;
Hose, James ;
Haroon, Suraiya ;
Gebbia, Marinella ;
Heisler, Lawrence E. ;
Nislow, Corey ;
Giaever, Guri ;
Gasch, Audrey P. .
PLOS GENETICS, 2011, 7 (11)