Literature DB >> 25483189

How MAP kinase modules function as robust, yet adaptable, circuits.

Tianhai Tian1, Angus Harding.   

Abstract

Genetic and biochemical studies have revealed that the diversity of cell types and developmental patterns evident within the animal kingdom is generated by a handful of conserved, core modules. Core biological modules must be robust, able to maintain functionality despite perturbations, and yet sufficiently adaptable for random mutations to generate phenotypic variation during evolution. Understanding how robust, adaptable modules have influenced the evolution of eukaryotes will inform both evolutionary and synthetic biology. One such system is the MAP kinase module, which consists of a 3-tiered kinase circuit configuration that has been evolutionarily conserved from yeast to man. MAP kinase signal transduction pathways are used across eukaryotic phyla to drive biological functions that are crucial for life. Here we ask the fundamental question, why do MAPK modules follow a conserved 3-tiered topology rather than some other number? Using computational simulations, we identify a fundamental 2-tiered circuit topology that can be readily reconfigured by feedback loops and scaffolds to generate diverse signal outputs. When this 2-kinase circuit is connected to proximal input kinases, a 3-tiered modular configuration is created that is both robust and adaptable, providing a biological circuit that can regulate multiple phenotypes and maintain functionality in an uncertain world. We propose that the 3-tiered signal transduction module has been conserved through positive selection, because it facilitated the generation of phenotypic variation during eukaryotic evolution.

Entities:  

Keywords:  MAP kinase; evolution; facilitated variation; robustness; signal transduction; systems biology

Mesh:

Year:  2014        PMID: 25483189      PMCID: PMC4128883          DOI: 10.4161/cc.29349

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  72 in total

Review 1.  Signal transduction: hanging on a scaffold.

Authors:  W R Burack; A S Shaw
Journal:  Curr Opin Cell Biol       Date:  2000-04       Impact factor: 8.382

2.  Scaffold proteins may biphasically affect the levels of mitogen-activated protein kinase signaling and reduce its threshold properties.

Authors:  A Levchenko; J Bruck; P W Sternberg
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-23       Impact factor: 11.205

Review 3.  Mammalian MAPK signal transduction pathways activated by stress and inflammation: a 10-year update.

Authors:  John M Kyriakis; Joseph Avruch
Journal:  Physiol Rev       Date:  2012-04       Impact factor: 37.312

4.  The original Michaelis constant: translation of the 1913 Michaelis-Menten paper.

Authors:  Leonor Michaelis; Maud Leonora Menten; Kenneth A Johnson; Roger S Goody
Journal:  Biochemistry       Date:  2011-09-09       Impact factor: 3.162

5.  Why do protein kinase cascades have more than one level?

Authors:  G C Brown; J B Hoek; B N Kholodenko
Journal:  Trends Biochem Sci       Date:  1997-08       Impact factor: 13.807

6.  How responses get more switch-like as you move down a protein kinase cascade.

Authors:  J E Ferrell
Journal:  Trends Biochem Sci       Date:  1997-08       Impact factor: 13.807

7.  Multiple mitogen-activated protein kinase signaling pathways connect the cot oncoprotein to the c-jun promoter and to cellular transformation.

Authors:  M Chiariello; M J Marinissen; J S Gutkind
Journal:  Mol Cell Biol       Date:  2000-03       Impact factor: 4.272

8.  Identification and characterization of a novel MAP kinase kinase kinase, MLTK.

Authors:  I Gotoh; M Adachi; E Nishida
Journal:  J Biol Chem       Date:  2000-10-19       Impact factor: 5.157

9.  Bistability in the JNK cascade.

Authors:  C P Bagowski; J E Ferrell
Journal:  Curr Biol       Date:  2001-08-07       Impact factor: 10.834

10.  Variability and robustness in T cell activation from regulated heterogeneity in protein levels.

Authors:  Ofer Feinerman; Joël Veiga; Jeffrey R Dorfman; Ronald N Germain; Grégoire Altan-Bonnet
Journal:  Science       Date:  2008-08-22       Impact factor: 47.728

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  4 in total

1.  Analysis of mechanotransduction dynamics during combined mechanical stimulation and modulation of the extracellular-regulated kinase cascade uncovers hidden information within the signalling noise.

Authors:  Gianluca Ascolani; Timothy M Skerry; Damien Lacroix; Enrico Dall'Ara; Aban Shuaib
Journal:  Interface Focus       Date:  2020-12-11       Impact factor: 3.906

2.  Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway.

Authors:  Mathilde Guzzo; Rym Agrebi; Leon Espinosa; Grégory Baronian; Virginie Molle; Emilia M F Mauriello; Céline Brochier-Armanet; Tâm Mignot
Journal:  PLoS Genet       Date:  2015-08-20       Impact factor: 5.917

Review 3.  GPCR Signaling Regulation: The Role of GRKs and Arrestins.

Authors:  Vsevolod V Gurevich; Eugenia V Gurevich
Journal:  Front Pharmacol       Date:  2019-02-19       Impact factor: 5.810

Review 4.  c-Jun N-Terminal Kinase Inhibitors as Potential Leads for New Therapeutics for Alzheimer's Diseases.

Authors:  Stephanie Cristine Hepp Rehfeldt; Fernanda Majolo; Márcia Inês Goettert; Stefan Laufer
Journal:  Int J Mol Sci       Date:  2020-12-18       Impact factor: 6.208

  4 in total

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