Optogenetic actuator - ERK biosensor circuits identify MAPK network nodes that shape ERK dynamics

被引:23
作者
Dessauges, Coralie [1 ]
Mikelson, Jan [2 ]
Dobrzynski, Maciej [1 ]
Jacques, Marc-Antoine [1 ]
Frismantiene, Agne [1 ]
Gagliardi, Paolo Armando [1 ]
Khammash, Mustafa [2 ]
Pertz, Olivier [1 ]
机构
[1] Univ Bern, Inst Cell Biol, Bern, Switzerland
[2] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Basel, Switzerland
基金
欧盟地平线“2020”; 瑞士国家科学基金会;
关键词
ERK dynamics; MAPK network; optogenetics; signaling robustness; single-cell biology; NEGATIVE FEEDBACK-REGULATION; SPATIOTEMPORAL CONTROL; ERBB NETWORK; RAS; EXPRESSION; PHOSPHORYLATION; OSCILLATIONS; PHOSPHATASE; ACTIVATION; INHIBITOR;
D O I
10.15252/msb.202110670
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
Combining single-cell measurements of ERK activity dynamics with perturbations provides insights into the MAPK network topology. We built circuits consisting of an optogenetic actuator to activate MAPK signaling and an ERK biosensor to measure single-cell ERK dynamics. This allowed us to conduct RNAi screens to investigate the role of 50 MAPK proteins in ERK dynamics. We found that the MAPK network is robust against most node perturbations. We observed that the ERK-RAF and the ERK-RSK2-SOS negative feedback operate simultaneously to regulate ERK dynamics. Bypassing the RSK2-mediated feedback, either by direct optogenetic activation of RAS, or by RSK2 perturbation, sensitized ERK dynamics to further perturbations. Similarly, targeting this feedback in a human ErbB2-dependent oncogenic signaling model increased the efficiency of a MEK inhibitor. The RSK2-mediated feedback is thus important for the ability of the MAPK network to produce consistent ERK outputs, and its perturbation can enhance the efficiency of MAPK inhibitors.
引用
收藏
页数:22
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共 71 条
[41]  
Lam AJ, 2012, NAT METHODS, V9, P1005, DOI [10.1038/NMETH.2171, 10.1038/nmeth.2171]
[42]   NEGATIVE FEEDBACK-REGULATION AND DESENSITIZATION OF INSULIN-STIMULATED AND EPIDERMAL GROWTH FACTOR-STIMULATED P21(RAS) ACTIVATION [J].
LANGLOIS, WJ ;
SASAOKA, T ;
SALTIEL, AR ;
OLEFSKY, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (43) :25320-25323
[43]   ERK signalling: a master regulator of cell behaviour, life and fate [J].
Lavoie, Hugo ;
Gagnon, Jessica ;
Therrien, Marc .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2020, 21 (10) :607-632
[44]   The Dark Side of Cell Signaling: Positive Roles for Negative Regulators [J].
Lemmon, Mark A. ;
Freed, Daniel M. ;
Schlessinger, Joseph ;
Kiyatkin, Anatoly .
CELL, 2016, 164 (06) :1172-1184
[45]   CellProfiler 3.0: Next-generation image processing for biology [J].
McQuin, Claire ;
Goodman, Allen ;
Chernyshev, Vasiliy ;
Kamentsky, Lee ;
Cimini, Beth A. ;
Karhohs, Kyle W. ;
Doan, Minh ;
Ding, Liya ;
Rafelski, Susanne M. ;
Thirstrup, Derek ;
Wiegraebe, Winfried ;
Singh, Shantanu ;
Becker, Tim ;
Caicedo, Juan C. ;
Carpenter, Anne E. .
PLOS BIOLOGY, 2018, 16 (07)
[46]   Likelihood-free nested sampling for parameter inference of biochemical reaction networks [J].
Mikelson, Jan ;
Khammash, Mustafa .
PLOS COMPUTATIONAL BIOLOGY, 2020, 16 (10)
[47]   Ligand-Specific c-Fos Expression Emerges from the Spatiotemporal Control of ErbB Network Dynamics [J].
Nakakuki, Takashi ;
Birtwistle, Marc R. ;
Saeki, Yuko ;
Yumoto, Noriko ;
Ide, Kaori ;
Nagashima, Takeshi ;
Brusch, Lutz ;
Ogunnaike, Babatunde A. ;
Okada-Hatakeyama, Mariko ;
Kholodenko, Boris N. .
CELL, 2010, 141 (05) :884-896
[48]   Systematic Functional Annotation of Somatic Mutations in Cancer [J].
Ng, Patrick Kwok-Shing ;
Li, Jun ;
Jeong, Kang Jin ;
Shao, Shan ;
Chen, Hu ;
Tsang, Yiu Huen ;
Sengupta, Sohini ;
Wang, Zixing ;
Bhavana, Venkata Hemanjani ;
Tran, Richard ;
Soewito, Stephanie ;
Minussi, Darlan Conterno ;
Moreno, Daniela ;
Kong, Kathleen ;
Dogruluk, Turgut ;
Lu, Hengyu ;
Gao, Jianjiong ;
Tokheim, Collin ;
Zhou, Daniel Cui ;
Johnson, Amber M. ;
Zeng, Jia ;
Ip, Carman Ka Man ;
Ju, Zhenlin ;
Wester, Matthew ;
Yu, Shuangxing ;
Li, Yongsheng ;
Vellano, Christopher P. ;
Schultz, Nikolaus ;
Karchin, Rachel ;
Ding, Li ;
Lu, Yiling ;
Cheung, Lydia Wai Ting ;
Chen, Ken ;
Shaw, Kenna R. ;
Meric-Bernstam, Funda ;
Scott, Kenneth L. ;
Yi, Song ;
Sahni, Nidhi ;
Liang, Han ;
Mills, Gordon B. .
CANCER CELL, 2018, 33 (03) :450-+
[49]   The Fibroblast Growth Factor signaling pathway [J].
Ornitz, David M. ;
Itoh, Nobuyuki .
WILEY INTERDISCIPLINARY REVIEWS-DEVELOPMENTAL BIOLOGY, 2015, 4 (03) :215-266
[50]   Computational modelling of the receptor-tyrosine-kinase-activated MAPK pathway [J].
Orton, RJ ;
Sturm, OE ;
Vyshemirsky, V ;
Calder, M ;
Gilbert, DR ;
Kolch, W .
BIOCHEMICAL JOURNAL, 2005, 392 :249-261