C-Jun N-terminal kinases

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mitogen-activated protein kinase 8
Identifiers
SymbolMAPK8
Alt. symbolsPRKM8
Entrez5599
HUGO6881
OMIM601158
RefSeqNM_002750
UniProtP45983
Other data
LocusChr. 10 q11.2
mitogen-activated protein kinase 9
Identifiers
SymbolMAPK9
Alt. symbolsPRKM9
Entrez5601
HUGO6886
OMIM602896
RefSeqNM_002752
UniProtP45984
Other data
LocusChr. 5 q35
mitogen-activated protein kinase 10
Identifiers
SymbolMAPK10
Alt. symbolsPRKM10
Entrez5602
HUGO6872
OMIM602897
RefSeqNM_002753
UniProtP53779
Other data
LocusChr. 4 q22-q23


Overview

C-Jun N-terminal kinases (JNKs), originally identified as kinases that bind and phosphosphorylate c-Jun on Ser63 and Ser73 within its transcriptional activation domain, are mitogen-activated protein kinases which are responsive to stress stimuli, such as cytokines, ultraviolet irradiation, heat shock, and osmotic shock, and are involved in T cell differentiation and apoptosis.

Isoforms

The c-Jun N-terminal kinases consist of ten isoforms deriving from the three genes JNK1, JNK2 and JNK3[1]:

  • JNK1 and JNK2 are ubiquitously distributed.
  • By contrast, JNK3 is found mainly in neuronal tissue and testes.

Functions

JNK1 is involved in apoptosis, neurodegeneration, cell differentiation and proliferation, inflammatory conditions and cytokine production mediated by AP-1 (Activation Protein 1) such as RANTES, IL-8 and GM-CSF. [2]

Recently, JNK1 has been found to regulate Jun protein turnover by phosphorylation and activation of the ubiquitin ligase Itch.

JNKs can associate with scaffold proteins JNK Interacting Proteins as well as their upstream kinases JNKK1 and JNKK2 following their activation.

External links

References

  1. Waetzig V, Herdegen T (2005). "Context-specific inhibition of JNKs: overcoming the dilemma of protection and damage". Br. J. Pharmacol. 26 (9): 455–61. PMID 16054242.
  2. Oltmanns U, Issa R, Sukkar M, John M, Chung K (2003). "Role of c-jun N-terminal kinase in the induced release of GM-CSF, RANTES and IL-8 from human airway smooth muscle cells" (PDF). Br. J. Pharmacol. 139 (6): 1228–34. PMID 12871843.

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