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Sensitivity control through attenuation of signal transfer efficiency by negative regulation of cellular signalling
Open accessAbstract
Sensitivity is one of the hallmarks of biological and pharmacological responses. However, the principle of controlling sensitivity remains unclear. Here we theoretically analyse a simple biochemical reaction and find that the signal transfer efficiency of the transient peak amplitude attenuates depending on the strength of negative regulation. We experimentally find that many signalling pathways in various cell lines, including the Akt and ERK pathways, can be approximated by simple biochemical reactions and that the same property of the attenuation of signal transfer efficiency was observed for such pathways. Because of this property, a downstream molecule should show higher sensitivity to an activator and lower sensitivity to an inhibitor than an upstream molecule. Indeed, we experimentally verify that S6, which lies downstream of Akt, shows lower sensitivity to an epidermal growth factor receptor inhibitor than Akt. Thus, cells can control downstream sensitivity through the attenuation of signal transfer efficiency by changing the expression level of negative regulators.
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“In further support earlier studies [46] found that a downstream molecule can be more sensitive to an upstream activator than the direct target molecule of the activator.”
From Maximizing the information content of experiments in systems biology (2013) · cites this paper as [46]
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References 29 · Cited by 21
Metadata
- Authors
- Toyoshima, Y., Kakuda, H., Fujita, K. A., Uda, S., & Kuroda, S.
- Affiliations
- The University of Tokyo (JP)
- Japan Science and Technology Agency (JP)
- Corresponding author
- Kuroda, Shinya
- Venue
- Nature Communications
- Published
- 2012-03-13
- Volume
- 3
- Issue
- 1
- Pages
- 743-743
- ISSN
- 2041-1723 (ISSN-L)
- OpenAlex
- W2026992340
- Cited by
- 21
- References
- 29
- Citations by year
- 2021: 1 · 2020: 3 · 2019: 1 · 2018: 1 · 2017: 3 · 2016: 2 · 2015: 2 · 2014: 3 · 2013: 4 · 2012: 1
- FWCI
- 1.28
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Nature Communications (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology (21240025, CREST)
- Japan Society for the Promotion of Science (CREST, 21240025)
- Core Research for Evolutional Science and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- sensitivity control, negative regulation, signal transduction, AKT pathway, ERK signaling, ribosomal protein S6, EGFR inhibitors, biochemical reaction models
- MeSH terms
- Lapatinib, Animals, Cell Line, HeLa Cells, Humans, Models, Biological, Quinazolines, Signal Transduction, 3T3 Cells, MAP Kinase Signaling System, Cell Line, Tumor, Protein Kinase Inhibitors, Extracellular Signal-Regulated MAP Kinases, Proto-Oncogene Proteins c-akt, Mice, Rats, ErbB Receptors
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