Deletion of the transcription factors Hsf1, Msn2 and Msn4 in yeast uncovers transcriptional reprogramming in response to proteotoxic stress

被引:4
作者
Muehlhofer, Moritz [1 ]
Offensperger, Felix [2 ]
Reschke, Sarah [3 ]
Wallmann, Georg [2 ]
Csaba, Gergely [2 ]
Berchtold, Evi [2 ]
Riedl, Maximilian [1 ]
Blum, Helmut [3 ]
Haslbeck, Martin [1 ]
Zimmer, Ralf [2 ]
Buchner, Johannes [1 ]
机构
[1] Tech Univ Munich, Ctr Prot Assemblies, Dept Biosci, Ernst Otto Fischer Str 8, D-85747 Garching, Germany
[2] Ludwig Maximilians Univ Munchen, Inst Bioinformat, Dept Informat, Munich, Germany
[3] LMU Munchen, Gene Ctr, Lab Funct Genome Anal, Munich, Germany
关键词
heat shock response; Hsf1; Msn2/4; transcriptome; proteome; proteostasis; HEAT-SHOCK RESPONSE; DNA-BINDING PROTEIN; SACCHAROMYCES-CEREVISIAE; MOLECULAR CHAPERONES; SIGNALING PATHWAYS; OXIDATIVE STRESS; GENE; EXPRESSION; INDUCTION; LIFE;
D O I
10.1002/1873-3468.14821
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The response to proteotoxic stresses such as heat shock allows organisms to maintain protein homeostasis under changing environmental conditions. We asked what happens if an organism can no longer react to cytosolic proteotoxic stress. To test this, we deleted or depleted, either individually or in combination, the stress-responsive transcription factors Msn2, Msn4, and Hsf1 in Saccharomyces cerevisiae. Our study reveals a combination of survival strategies, which together protect essential proteins. Msn2 and 4 broadly reprogram transcription, triggering the response to oxidative stress, as well as biosynthesis of the protective sugar trehalose and glycolytic enzymes, while Hsf1 mainly induces the synthesis of molecular chaperones and reverses the transcriptional response upon prolonged mild heat stress (adaptation). What happens if an organism can no longer react to cytosolic proteotoxic stress? To answer this question, we deleted or depleted the stress-responsive transcription factors Msn2, Msn4 and Hsf1 in S. cerevisiae. We show that Msn2/4 broadly reprogram transcription while Hsf1 induces mainly the synthesis of molecular chaperones and reverses the transcriptional response upon prolonged mild heat stress (adaptation). image
引用
收藏
页码:635 / 657
页数:23
相关论文
共 96 条
[11]   Msn2p and Msn4p control a large number of genes induced at the diauxic transition which are repressed by cyclic AMP in Saccharomyces cerevisiae [J].
Boy-Marcotte, E ;
Perrot, M ;
Bussereau, F ;
Boucherie, H ;
Jacquet, M .
JOURNAL OF BACTERIOLOGY, 1998, 180 (05) :1044-1052
[12]   Structure and function of a transcriptional network activated by the MAPK Hog1 [J].
Capaldi, Andrew P. ;
Kaplan, Tommy ;
Liu, Ying ;
Habib, Naomi ;
Regev, Aviv ;
Friedman, Nir ;
O'Shea, Erin K. .
NATURE GENETICS, 2008, 40 (11) :1300-1306
[13]   Dynamic 3D proteomes reveal protein functional alterations at high resolution in situ [J].
Cappelletti, Valentina ;
Hauser, Thomas ;
Piazza, Ilaria ;
Pepelnjak, Monika ;
Malinovska, Liliana ;
Fuhrer, Tobias ;
Li, Yaozong ;
Doerig, Christian ;
Boersema, Paul ;
Gillet, Ludovic ;
Grossbach, Jan ;
Dugourd, Aurelien ;
Saez-Rodriguez, Julio ;
Beyer, Andreas ;
Zamboni, Nicola ;
Caflisch, Amedeo ;
de Souza, Natalie ;
Picotti, Paola .
CELL, 2021, 184 (02) :545-+
[14]   Thermotolerant yeasts selected by adaptive evolution express heat stress response at 30°C [J].
Caspeta, Luis ;
Chen, Yun ;
Nielsen, Jens .
SCIENTIFIC REPORTS, 2016, 6
[15]   Remodeling of yeast genome expression in response to environmental changes [J].
Causton, HC ;
Ren, B ;
Koh, SS ;
Harbison, CT ;
Kanin, E ;
Jennings, EG ;
Lee, TI ;
True, HL ;
Lander, ES ;
Young, RA .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (02) :323-337
[16]   Function and regulation in MAPK signaling pathways:: Lessons learned from the yeast Saccharomyces cerevisiae [J].
Chen, Raymond E. ;
Thorner, Jeremy .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2007, 1773 (08) :1311-1340
[17]   Multiple decay events target HAC1 mRNA during splicing to regulate the unfolded protein response [J].
Cherry, Patrick D. ;
Peach, Sally E. ;
Hesselberth, Jay R. .
ELIFE, 2019, 8
[18]   Expression of a glutamate decarboxylase homologue is required for normal oxidative stress tolerance in Saccharomyces cerevisiae [J].
Coleman, ST ;
Fang, TK ;
Rovinsky, SA ;
Turano, FJ ;
Moye-Rowley, WS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (01) :244-250
[19]  
Collart M A, 2001, Curr Protoc Mol Biol, VChapter 13, DOI 10.1002/0471142727.mb1312s23
[20]   Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ [J].
Cox, Juergen ;
Hein, Marco Y. ;
Luber, Christian A. ;
Paron, Igor ;
Nagaraj, Nagarjuna ;
Mann, Matthias .
MOLECULAR & CELLULAR PROTEOMICS, 2014, 13 (09) :2513-2526