Literature DB >> 10523642

JSAP1, a novel jun N-terminal protein kinase (JNK)-binding protein that functions as a Scaffold factor in the JNK signaling pathway.

M Ito1, K Yoshioka, M Akechi, S Yamashita, N Takamatsu, K Sugiyama, M Hibi, Y Nakabeppu, T Shiba, K I Yamamoto.   

Abstract

The major components of the mitogen-activated protein kinase (MAPK) cascades are MAPK, MAPK kinase (MAPKK), and MAPKK kinase (MAPKKK). Recent rapid progress in identifying members of MAPK cascades suggests that a number of such signaling pathways exist in cells. To date, however, how the specificity and efficiency of the MAPK cascades is maintained is poorly understood. Here, we have identified a novel mouse protein, termed Jun N-terminal protein kinase (JNK)/stress-activated protein kinase-associated protein 1 (JSAP1), by a yeast two-hybrid screen, using JNK3 MAPK as the bait. Of the mammalian MAPKs tested (JNK1, JNK2, JNK3, ERK2, and p38alpha), JSAP1 preferentially coprecipitated with the JNKs in cotransfected COS-7 cells. JNK3 showed a higher binding affinity for JSAP1, compared with JNK1 and JNK2. In similar cotransfection studies, JSAP1 also interacted with SEK1 MAPKK and MEKK1 MAPKKK, which are involved in the JNK cascades. The regions of JSAP1 that bound JNK, SEK1, and MEKK1 were distinct from one another. JNK and MEKK1 also bound JSAP1 in vitro, suggesting that these interactions are direct. In contrast, only the activated form of SEK1 associated with JSAP1 in cotransfected COS-7 cells. The unstimulated SEK1 bound to MEKK1; thus, SEK1 might indirectly associate with JSAP1 through MEKK1. Although JSAP1 coprecipitated with MEK1 MAPKK and Raf-1 MAPKKK, and not MKK6 or MKK7 MAPKK, in cotransfected COS-7 cells, MEK1 and Raf-1 do not interfere with the binding of SEK1 and MEKK1 to JSAP1, respectively. Overexpression of full-length JSAP1 in COS-7 cells led to a considerable enhancement of JNK3 activation, and modest enhancement of JNK1 and JNK2 activation, by the MEKK1-SEK1 pathway. Deletion of the JNK- or MEKK1-binding regions resulted in a significant reduction in the enhancement of the JNK3 activation in COS-7 cells. These results suggest that JSAP1 functions as a scaffold protein in the JNK3 cascade. We also discuss a scaffolding role for JSAP1 in the JNK1 and JNK2 cascades.

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Year:  1999        PMID: 10523642      PMCID: PMC84763          DOI: 10.1128/MCB.19.11.7539

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  54 in total

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2.  Mitogen-activated protein kinase kinase 7 is an activator of the c-Jun NH2-terminal kinase.

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Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-08       Impact factor: 11.205

3.  Dimerization of Ste5, a mitogen-activated protein kinase cascade scaffold protein, is required for signal transduction.

Authors:  D Yablonski; I Marbach; A Levitzki
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4.  c-Jun can recruit JNK to phosphorylate dimerization partners via specific docking interactions.

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Review 5.  Mitogen-activated protein kinase pathways.

Authors:  M J Robinson; M H Cobb
Journal:  Curr Opin Cell Biol       Date:  1997-04       Impact factor: 8.382

6.  Cloning and characterization of MEK6, a novel member of the mitogen-activated protein kinase kinase cascade.

Authors:  B Stein; H Brady; M X Yang; D B Young; M S Barbosa
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Authors:  J Raingeaud; A J Whitmarsh; T Barrett; B Dérijard; R J Davis
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8.  MLK-3 activates the SAPK/JNK and p38/RK pathways via SEK1 and MKK3/6.

Authors:  L A Tibbles; Y L Ing; F Kiefer; J Chan; N Iscove; J R Woodgett; N J Lassam
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9.  Induction of apoptosis by ASK1, a mammalian MAPKKK that activates SAPK/JNK and p38 signaling pathways.

Authors:  H Ichijo; E Nishida; K Irie; P ten Dijke; M Saitoh; T Moriguchi; M Takagi; K Matsumoto; K Miyazono; Y Gotoh
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10.  Cloning of a novel mitogen-activated protein kinase kinase kinase, MEKK4, that selectively regulates the c-Jun amino terminal kinase pathway.

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Journal:  J Biol Chem       Date:  1997-03-28       Impact factor: 5.157

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  70 in total

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Journal:  Biochem J       Date:  2001-01-15       Impact factor: 3.857

2.  Eleven densely clustered genes, six of them novel, in 176 kb of mouse t-complex DNA.

Authors:  G J Kargul; R Nagaraja; T Shimada; M J Grahovac; M K Lim; H Nakashima; P Waeltz; P Ma; E Chen; D Schlessinger; M S Ko
Journal:  Genome Res       Date:  2000-07       Impact factor: 9.043

3.  Random monoallelic expression of three genes clustered within 60 kb of mouse t complex genomic DNA.

Authors:  Y Sano; T Shimada; H Nakashima; R H Nicholson; J F Eliason; T A Kocarek; M S Ko
Journal:  Genome Res       Date:  2001-11       Impact factor: 9.043

Review 4.  Multifaceted roles of beta-arrestins in the regulation of seven-membrane-spanning receptor trafficking and signalling.

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5.  Role of the JIP4 scaffold protein in the regulation of mitogen-activated protein kinase signaling pathways.

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Journal:  Mol Cell Biol       Date:  2005-04       Impact factor: 4.272

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7.  Pin1 in neuronal apoptosis.

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8.  Apoptosis Repressor With Caspase Recruitment Domain Ameliorates Amyloid-Induced β-Cell Apoptosis and JNK Pathway Activation.

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9.  c-Jun N-terminal kinases (JNK) antagonize cardiac growth through cross-talk with calcineurin-NFAT signaling.

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Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

10.  DNA damage during the spindle-assembly checkpoint degrades CDC25A, inhibits cyclin-CDC2 complexes, and reverses cells to interphase.

Authors:  Jeremy P H Chow; Wai Yi Siu; Tsz Kan Fung; Wan Mui Chan; Anita Lau; Talha Arooz; Chuen-Pei Ng; Katsumi Yamashita; Randy Y C Poon
Journal:  Mol Biol Cell       Date:  2003-07-25       Impact factor: 4.138

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