Mitogen-activated protein kinase: conservation of a three-kinase module from yeast to human - PubMed (original) (raw)
Review
Mitogen-activated protein kinase: conservation of a three-kinase module from yeast to human
C Widmann et al. Physiol Rev. 1999 Jan.
Free article
Abstract
Mitogen-activated protein kinases (MAPK) are serine-threonine protein kinases that are activated by diverse stimuli ranging from cytokines, growth factors, neurotransmitters, hormones, cellular stress, and cell adherence. Mitogen-activated protein kinases are expressed in all eukaryotic cells. The basic assembly of MAPK pathways is a three-component module conserved from yeast to humans. The MAPK module includes three kinases that establish a sequential activation pathway comprising a MAPK kinase kinase (MKKK), MAPK kinase (MKK), and MAPK. Currently, there have been 14 MKKK, 7 MKK, and 12 MAPK identified in mammalian cells. The mammalian MAPK can be subdivided into five families: MAPKerk1/2, MAPKp38, MAPKjnk, MAPKerk3/4, and MAPKerk5. Each MAPK family has distinct biological functions. In Saccharomyces cerevisiae, there are five MAPK pathways involved in mating, cell wall remodelling, nutrient deprivation, and responses to stress stimuli such as osmolarity changes. Component members of the yeast pathways have conserved counterparts in mammalian cells. The number of different MKKK in MAPK modules allows for the diversity of inputs capable of activating MAPK pathways. In this review, we define all known MAPK module kinases from yeast to humans, what is known about their regulation, defined MAPK substrates, and the function of MAPK in cell physiology.
Similar articles
- Inhibitory and activating functions for MAPK Kss1 in the S. cerevisiae filamentous-growth signalling pathway.
Cook JG, Bardwell L, Thorner J. Cook JG, et al. Nature. 1997 Nov 6;390(6655):85-8. doi: 10.1038/36355. Nature. 1997. PMID: 9363895 - Regulation of the Saccharomyces cerevisiae HOG1 mitogen-activated protein kinase by the PTP2 and PTP3 protein tyrosine phosphatases.
Wurgler-Murphy SM, Maeda T, Witten EA, Saito H. Wurgler-Murphy SM, et al. Mol Cell Biol. 1997 Mar;17(3):1289-97. doi: 10.1128/MCB.17.3.1289. Mol Cell Biol. 1997. PMID: 9032256 Free PMC article. - Mammalian MAP kinase modules: how to transduce specific signals.
Brunet A, Pouysségur J. Brunet A, et al. Essays Biochem. 1997;32:1-16. Essays Biochem. 1997. PMID: 9493007 Review. - MAP kinase pathways in yeast: for mating and more.
Herskowitz I. Herskowitz I. Cell. 1995 Jan 27;80(2):187-97. doi: 10.1016/0092-8674(95)90402-6. Cell. 1995. PMID: 7834739 Review. No abstract available.
Cited by
- Cellular and Molecular Mechanisms of Hypertrophy of Ligamentum Flavum.
Silwal P, Nguyen-Thai AM, Alexander PG, Sowa GA, Vo NV, Lee JY. Silwal P, et al. Biomolecules. 2024 Oct 10;14(10):1277. doi: 10.3390/biom14101277. Biomolecules. 2024. PMID: 39456209 Free PMC article. Review. - Understanding the Genetic Landscape of Gestational Diabetes: Insights into the Causes and Consequences of Elevated Glucose Levels in Pregnancy.
Brito Nunes C, Borges MC, Freathy RM, Lawlor DA, Qvigstad E, Evans DM, Moen GH. Brito Nunes C, et al. Metabolites. 2024 Sep 20;14(9):508. doi: 10.3390/metabo14090508. Metabolites. 2024. PMID: 39330515 Free PMC article. Review. - Post-Translational Modification of WRKY Transcription Factors.
Zhou X, Lei Z, An P. Zhou X, et al. Plants (Basel). 2024 Jul 25;13(15):2040. doi: 10.3390/plants13152040. Plants (Basel). 2024. PMID: 39124158 Free PMC article. Review. - Targeting the multifaceted BRAF in cancer: New directions.
Toye E, Chehrazi-Raffle A, Hwang J, Antonarakis ES. Toye E, et al. Oncotarget. 2024 Jul 16;15:486-492. doi: 10.18632/oncotarget.28612. Oncotarget. 2024. PMID: 39018217 Free PMC article. Review. - N-methyl-D-aspartate Receptor Subunits 2A and 2B Mediate Connexins and Pannexins in the Trigeminal Ganglion Involved in Orofacial Inflammatory Allodynia during Temporomandibular Joint Inflammation.
Li YL, Zhang YY, Song QX, Liu F, Liu YJ, Li YK, Zhou C, Shen JF. Li YL, et al. Mol Neurobiol. 2024 Jul 8. doi: 10.1007/s12035-024-04291-5. Online ahead of print. Mol Neurobiol. 2024. PMID: 38976127
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases