Literature DB >> 16571722

Direct interaction of the molecular scaffolds POSH and JIP is required for apoptotic activation of JNKs.

Nickolay V Kukekov1, Zhiheng Xu, Lloyd A Greene.   

Abstract

A sequential pathway (the JNK pathway) that includes activation of Rac1/Cdc42, mixed lineage kinases, MAP kinase kinases 4 and 7, and JNKs plays a required role in many paradigms of apoptotic cell death. However, the means by which this pathway is assembled and directed toward apoptotic death has been unclear. Here, we report that propagation of the apoptotic JNK pathway requires the cooperative interaction of two molecular scaffolds, POSH and JIPs. POSH (plenty of SH3s) is a multidomain GTP-Rac1-interacting protein that binds and promotes activation of mixed lineage kinases. JIPs are reported to bind MAP kinase kinases 4/7 and JNKs. We find that POSH and JIPs directly associate with one another to form a multiprotein complex, PJAC (POSH-JIP apoptotic complex), that includes all of the known kinase components of the pathway. Our observations indicate that this complex is required for JNK activation and cell death in response to apoptotic stimuli.

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Year:  2006        PMID: 16571722     DOI: 10.1074/jbc.M601056200

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


  25 in total

Review 1.  The c-jun kinase/stress-activated pathway: regulation, function and role in human disease.

Authors:  Gary L Johnson; Kazuhiro Nakamura
Journal:  Biochim Biophys Acta       Date:  2007-01-04

Review 2.  The role of scaffold proteins in JNK signalling.

Authors:  W Engström; A Ward; K Moorwood
Journal:  Cell Prolif       Date:  2009-11-17       Impact factor: 6.831

3.  Regulation of the protein stability of POSH and MLK family.

Authors:  Chunyan Wang; Yang Tao; Yaqing Wang; Zhiheng Xu
Journal:  Protein Cell       Date:  2010-10-07       Impact factor: 14.870

4.  A novel regulator of ER Ca2+ drives Hippo-mediated tumorigenesis.

Authors:  Xianjue Ma; Jin-Yu Lu; Alexandra Moraru; Aurelio A Teleman; Jinan Fang; Yue Qiu; Peng Liu; Tian Xu
Journal:  Oncogene       Date:  2019-10-24       Impact factor: 9.867

5.  POSH Regulates CD4+ T Cell Differentiation and Survival.

Authors:  Cody A Cunningham; Leah N Cardwell; Yue Guan; Emma Teixeiro; Mark A Daniels
Journal:  J Immunol       Date:  2016-04-15       Impact factor: 5.422

6.  Sh3rf2/POSHER protein promotes cell survival by ring-mediated proteasomal degradation of the c-Jun N-terminal kinase scaffold POSH (Plenty of SH3s) protein.

Authors:  Michael Wilhelm; Nickolay V Kukekov; Travis L Schmit; Katherine V Biagas; Andrew A Sproul; Stephen Gire; Margaret E Maes; Zhiheng Xu; Lloyd A Greene
Journal:  J Biol Chem       Date:  2011-11-28       Impact factor: 5.157

7.  POSH misexpression induces caspase-dependent cell death in Drosophila.

Authors:  Ashley L Lennox; Beth Stronach
Journal:  Dev Dyn       Date:  2010-02       Impact factor: 3.780

8.  Identification and analysis of a novel dimerization domain shared by various members of c-Jun N-terminal kinase (JNK) scaffold proteins.

Authors:  Ksenya Cohen-Katsenelson; Tanya Wasserman; Ilona Darlyuk-Saadon; Alona Rabner; Fabian Glaser; Ami Aronheim
Journal:  J Biol Chem       Date:  2013-01-22       Impact factor: 5.157

9.  Kalirin-7, a protein enriched in postsynaptic density, is involved in ischemic signal transduction.

Authors:  Małgorzata Beresewicz; Joanna E Kowalczyk; Barbara Zabłocka
Journal:  Neurochem Res       Date:  2008-03-13       Impact factor: 3.996

10.  Cbl negatively regulates JNK activation and cell death.

Authors:  Andrew A Sproul; Zhiheng Xu; Michael Wilhelm; Stephen Gire; Lloyd A Greene
Journal:  Cell Res       Date:  2009-08       Impact factor: 25.617

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