Literature DB >> 9024636

MEKKs, GCKs, MLKs, PAKs, TAKs, and tpls: upstream regulators of the c-Jun amino-terminal kinases?

G R Fanger1, P Gerwins, C Widmann, M B Jarpe, G L Johnson.   

Abstract

Regulation of the mitogen-activated protein kinase (MAPK) family members - which include the extracellular response kinases (ERKs), p38/HOG1, and the c-Jun amino-terminal kinases (JNKs) - plays a central role in mediating the effects of diverse stimuli encompassing cytokines, hormones, growth factors and stresses such as osmotic imbalance, heat shock, inhibition of protein synthesis and irradiation. A rapidly increasing number of kinases that activate the JNK pathways has been described recently, including the MAPK/ERK kinase kinases, p21-activated kinases, germinal center kinase, mixed lineage kinases, tumor progression locus 2, and TGF-beta-activated kinase. Thus, regulation of the JNK pathway provides an interesting example of how many different stimuli can converge into regulating pathways critical for the determination of cell fate.

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Year:  1997        PMID: 9024636     DOI: 10.1016/s0959-437x(97)80111-6

Source DB:  PubMed          Journal:  Curr Opin Genet Dev        ISSN: 0959-437X            Impact factor:   5.578


  62 in total

1.  Functional characterization of the interaction of Ste50p with Ste11p MAPKKK in Saccharomyces cerevisiae.

Authors:  C Wu; E Leberer; D Y Thomas; M Whiteway
Journal:  Mol Biol Cell       Date:  1999-07       Impact factor: 4.138

2.  Expression and activation of mitogen-activated protein kinase kinases-3 and -6 in rheumatoid arthritis.

Authors:  Martine Chabaud-Riou; Gary S Firestein
Journal:  Am J Pathol       Date:  2004-01       Impact factor: 4.307

Review 3.  Signal transduction networks in rheumatoid arthritis.

Authors:  D Hammaker; S Sweeney; G S Firestein
Journal:  Ann Rheum Dis       Date:  2003-11       Impact factor: 19.103

4.  Stress- and cell type-dependent regulation of transfected c-Jun N-terminal kinase and mitogen-activated protein kinase kinase isoforms.

Authors:  L Butterfield; E Zentrich; A Beekman; L E Heasley
Journal:  Biochem J       Date:  1999-03-15       Impact factor: 3.857

5.  Activation of CD95 (APO-1/Fas) signaling by ceramide mediates cancer therapy-induced apoptosis.

Authors:  I Herr; D Wilhelm; T Böhler; P Angel; K M Debatin
Journal:  EMBO J       Date:  1997-10-15       Impact factor: 11.598

6.  c-Jun N-terminal kinase is required for metalloproteinase expression and joint destruction in inflammatory arthritis.

Authors:  Z Han; D L Boyle; L Chang; B Bennett; M Karin; L Yang; A M Manning; G S Firestein
Journal:  J Clin Invest       Date:  2001-07       Impact factor: 14.808

7.  The MKK7 gene encodes a group of c-Jun NH2-terminal kinase kinases.

Authors:  C Tournier; A J Whitmarsh; J Cavanagh; T Barrett; R J Davis
Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

8.  Cloning and characterization of GETS-1, a goldfish Ets family member that functions as a transcriptional repressor in muscle.

Authors:  D Goldman; M K Sapru; S Stewart; J Plotkin; T A Libermann; B Wasylyk; K Guan
Journal:  Biochem J       Date:  1998-10-15       Impact factor: 3.857

Review 9.  Signal transduction of stress via ceramide.

Authors:  S Mathias; L A Peña; R N Kolesnick
Journal:  Biochem J       Date:  1998-11-01       Impact factor: 3.857

10.  PRAK, a novel protein kinase regulated by the p38 MAP kinase.

Authors:  L New; Y Jiang; M Zhao; K Liu; W Zhu; L J Flood; Y Kato; G C Parry; J Han
Journal:  EMBO J       Date:  1998-06-15       Impact factor: 11.598

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