Literature DB >> 8824197

The small GTP-binding protein rho activates c-Jun N-terminal kinases/stress-activated protein kinases in human kidney 293T cells. Evidence for a Pak-independent signaling pathway.

H Teramoto1, P Crespo, O A Coso, T Igishi, N Xu, J S Gutkind.   

Abstract

Work from a number of laboratories has established a role for certain small GTP-binding proteins in controlling the enzymatic activity of a family of serine-threonine kinases known as mitogen-activated protein kinases (MAPKs). MAPKs have been classified into three subfamilies: extracellular signal-regulated kinases (ERKs), also known as MAPKs; c-Jun N-terminal kinases (JNKs); and p38 kinase. Whereas Ras controls the activation of MAPKs, we and others have recently observed that in certain cells, the small GTP-binding proteins Rac1 and Cdc42 but not Rho regulate the activity of JNKs. Furthermore, because Rac1 and Cdc42 but not Rho bind and activate a kinase known as Pak1, it has been suggested that Pak1 is the most upstream component of the pathway linking these GTPases to JNK. However, in both yeast and mammalian cells, Rho1p, a Rho homologue, and RhoA, respectively, directly interact with a number of proteins, including kinases related to protein kinase C. In addition, in yeast, Rho1p controls the activity of a MAPK cascade involved in bud formation. Considering this diversity of target molecules for small GTP-binding proteins, their likely tissue specific distribution, and the potential role for Rho in signaling to a kinase cascade, we decided to extend our initial analysis, exploring the ability of Ras and Rho-related GTP-binding proteins to activate MAPK or JNK in a variety of cell lines. We found that in the human kidney epithelial cell line, 293T, Cdc42 and all Rho proteins, RhoA, RhoB, and RhoC, but not Rac or Ras can induce activation of JNK. Furthermore, we provide evidence that signaling from Rho proteins to JNK in 293T cells does not involve Pak1. Taken together these findings demonstrate that Rho signals to JNK in a cell type-specific manner and suggest the existence of a novel, Pak1-independent signaling route communicating the Rho family of small GTP-binding proteins to the JNK pathway.

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Year:  1996        PMID: 8824197     DOI: 10.1074/jbc.271.42.25731

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  32 in total

1.  Interactions of protein kinase CK2 subunits.

Authors:  I Korn; S Gutkind; N Srinivasan; T L Blundell; C C Allende; J E Allende
Journal:  Mol Cell Biochem       Date:  1999-01       Impact factor: 3.396

2.  Critical activities of Rac1 and Cdc42Hs in skeletal myogenesis: antagonistic effects of JNK and p38 pathways.

Authors:  M Meriane; P Roux; M Primig; P Fort; C Gauthier-Rouvière
Journal:  Mol Biol Cell       Date:  2000-08       Impact factor: 4.138

3.  The hematopoiesis-specific GTP-binding protein RhoH is GTPase deficient and modulates activities of other Rho GTPases by an inhibitory function.

Authors:  Xiaoyu Li; Xia Bu; Binfeng Lu; Hava Avraham; Richard A Flavell; Bing Lim
Journal:  Mol Cell Biol       Date:  2002-02       Impact factor: 4.272

4.  Statin-induced inhibition of the Rho-signaling pathway activates PPARalpha and induces HDL apoA-I.

Authors:  G Martin; H Duez; C Blanquart; V Berezowski; P Poulain; J C Fruchart; J Najib-Fruchart; C Glineur; B Staels
Journal:  J Clin Invest       Date:  2001-06       Impact factor: 14.808

5.  G protein beta gamma subunit-dependent Rac-guanine nucleotide exchange activity of Ras-GRF1/CDC25(Mm).

Authors:  M Kiyono; T Satoh; Y Kaziro
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

6.  Nuclear targeting of a bacterial integrase that mediates site-specific recombination between bacterial and human target sequences.

Authors:  Leticia Agúndez; Cristina Machón; Carolina Elvira César; Manuel Rosa-Garrido; M Dolores Delgado; Matxalen Llosa
Journal:  Appl Environ Microbiol       Date:  2010-10-29       Impact factor: 4.792

7.  Elevated expression of cellular SYNE1, MMP10, and GTPase1 and their regulatory role in hepatocellular carcinoma progression.

Authors:  Laila H Faraj Shaglouf; Maryam Ranjpour; Saima Wajid; Swatantra Kumar Jain
Journal:  Protoplasma       Date:  2019-08-19       Impact factor: 3.356

8.  PAK promotes morphological changes by acting upstream of Rac.

Authors:  A Obermeier; S Ahmed; E Manser; S C Yen; C Hall; L Lim
Journal:  EMBO J       Date:  1998-08-03       Impact factor: 11.598

9.  A new rac target POSH is an SH3-containing scaffold protein involved in the JNK and NF-kappaB signalling pathways.

Authors:  N Tapon; K Nagata; N Lamarche; A Hall
Journal:  EMBO J       Date:  1998-03-02       Impact factor: 11.598

10.  Activation of hPAK65 by caspase cleavage induces some of the morphological and biochemical changes of apoptosis.

Authors:  N Lee; H MacDonald; C Reinhard; R Halenbeck; A Roulston; T Shi; L T Williams
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-09       Impact factor: 11.205

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