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c-Jun N-terminal kinases

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Main article: Mitogen-activated protein kinase
mitogen-activated protein kinase 8
Identifiers
SymbolMAPK8
Alt. symbolsJNK1, PRKM8
NCBI gene5599
HGNC6881
OMIM601158
RefSeqNM_002750
UniProtP45983
Other data
LocusChr. 10 q11.2
Search for
StructuresSwiss-model
DomainsInterPro
mitogen-activated protein kinase 9
Identifiers
SymbolMAPK9
Alt. symbolsJNK2, PRKM9
NCBI gene5601
HGNC6886
OMIM602896
RefSeqNM_002752
UniProtP45984
Other data
LocusChr. 5 q35
Search for
StructuresSwiss-model
DomainsInterPro
mitogen-activated protein kinase 10
Identifiers
SymbolMAPK10
Alt. symbolsJNK3, PRKM10
NCBI gene5602
HGNC6872
OMIM602897
RefSeqNM_002753
UniProtP53779
Other data
LocusChr. 4 q22-q23
Search for
StructuresSwiss-model
DomainsInterPro

c-Jun N-terminal kinases (JNKs), were originally identified as kinases that bind and phosphorylate c-Jun on Ser-63 and Ser-73 within its transcriptional activation domain. They belong to the mitogen-activated protein kinase family, and are responsive to stress stimuli, such as cytokines, ultraviolet irradiation, heat shock, and osmotic shock. They also play a role in T cell differentiation and the cellular apoptosis pathway. Activation occurs through a dual phosphorylation of threonine (Thr) and tyrosine (Tyr) residues within a Thr-Pro-Tyr motif located in kinase subdomain VIII. Activation is carried out by two MAP kinase kinases, MKK4 and MKK7, and JNK can be inactivated by Ser/Thr and Tyr protein phosphatases.[1] It has been suggested that this signaling pathway contributes to inflammatory responses in mammals and insects. [citation needed]

Isoforms

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The c-Jun N-terminal kinases consist of ten isoforms derived from three genes: JNK1 (four isoforms), JNK2 (four isoforms) and JNK3 (two isoforms).[2] Each gene is expressed as either 46 kDa or 55 kDa protein kinases, depending upon how the 3' coding region of the corresponding mRNA is processed. There have been no functional differences documented between the 46 kDa and the 55 kDa isoform, however, a second form of alternative splicing occurs within transcripts of JNK1 and JNK2, yielding JNK1-α, JNK2-α and JNK1-β and JNK2-β. Differences in interactions with protein substrates arise because of the mutually exclusive utilization of two exons within the kinase domain.[1]

c-Jun N-terminal kinase isoforms have the following tissue distribution:

  • JNK1 and JNK2 are found in all cells and tissues.[3]
  • JNK3 is found mainly in the brain, but is also found in the heart and the testes.[3]

Function

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Inflammatory signals, changes in levels of reactive oxygen species, ultraviolet radiation, protein synthesis inhibitors, and a variety of stress stimuli can activate JNK. One way this activation may occur is through disruption of the conformation of sensitive protein phosphatase enzymes; specific phosphatases normally inhibit the activity of JNK itself and the activity of proteins linked to JNK activation.[4]

JNKs can associate with scaffold proteins JNK interacting proteins (JIP) as well as their upstream kinases JNKK1 and JNKK2 following their activation.

JNK, by phosphorylation, modifies the activity of numerous proteins that reside at the mitochondria or act in the nucleus. Downstream molecules that are activated by JNK include c-Jun, ATF2, ELK1, SMAD4, p53 and HSF1. The downstream molecules that are inhibited by JNK activation include NFAT4, NFATC1 and STAT3. By activating and inhibiting other small molecules in this way, JNK activity regulates several important cellular functions including cell growth, differentiation, survival and apoptosis.

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.[5]

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

Neurotrophin binding to p75NTR activates a JNK signaling pathway causing apoptosis of developing neurons. JNK, through a series of intermediates, activates p53 and p53 activates Bax which initiates apoptosis. TrkA can prevent p75NTR-mediated JNK pathway apoptosis.[6] JNK can directly phosphorylate Bim-EL, a splicing isoform of Bcl-2 interacting mediator of cell death (Bim), which activates Bim-EL apoptotic activity. JNK activation is required for apoptosis but c-jun, a protein involved in the JNK pathway, is not always required.[7]

Roles in DNA repair

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The packaging of eukaryotic DNA into chromatin presents a barrier to all DNA-based processes that require recruitment of enzymes to their sites of action. To allow repair of double-strand breaks in DNA, the chromatin must be remodeled.[8] Chromatin relaxation occurs rapidly at the site of a DNA damage.[9] In one of the earliest steps, JNK phosphorylates SIRT6 on serine 10 in response to double-strand breaks (DSBs) or other DNA damage, and this step is required for efficient repair of DSBs.[10] Phosphorylation of SIRT6 on S10 facilitates the mobilization of SIRT6 to DNA damage sites, where SIRT6 then recruits and mono-phosphorylates poly (ADP-ribose) polymerase 1 (PARP1) at DNA break sites.[10] Half maximum accumulation of PARP1 occurs within 1.6 seconds after the damage occurs.[11] The chromatin remodeler Alc1 quickly attaches to the product of PARP1 action, a poly-ADP ribose chain,[9] allowing half of the maximum chromatin relaxation, presumably due to action of Alc1, by 10 seconds.[9] This allows recruitment of the DNA repair enzyme MRE11, to initiate DNA repair, within 13 seconds.[11]

Removal of UV-induced DNA photoproducts, during transcription coupled nucleotide excision repair (TC-NER), depends on JNK phosphorylation of DGCR8 on serine 153.[12] While DGCR8 is usually known to function in microRNA biogenesis, the microRNA-generating activity of DGCR8 is not required for DGCR8-dependent removal of UV-induced photoproducts.[12] Nucleotide excision repair is also needed for repair of oxidative DNA damage due to hydrogen peroxide (H2O2), and DGCR8 depleted cells are sensitive to H2O2.[12]

In aging

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In Drosophila, flies with mutations that augment JNK signaling accumulate less oxidative damage and live dramatically longer than wild-type flies.[13][14]

In the tiny roundworm Caenorhabditis elegans, loss-of-function mutants of JNK-1 have a decreased life span, while amplified expression of wild-type JNK-1 extends life span by 40%.[15] Worms with overexpressed JNK-1 also have significantly increased resistance to oxidative stress and other stresses.[15]

See also

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References

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  1. ^ a b Ip YT, Davis RJ (April 1998). "Signal transduction by the c-Jun N-terminal kinase (JNK)--from inflammation to development". Curr. Opin. Cell Biol. 10 (2): 205–19. doi:10.1016/S0955-0674(98)80143-9. PMID 9561845.
  2. ^ Waetzig V, Herdegen T (2005). "Context-specific inhibition of JNKs: overcoming the dilemma of protection and damage". Br. J. Pharmacol. 26 (9): 455–61. doi:10.1016/j.tips.2005.07.006. PMID 16054242.
  3. ^ a b Bode AM, Dong Z (August 2007). "The Functional Contrariety of JNK". Mol. Carcinog. 46 (8): 591–8. doi:10.1002/mc.20348. PMC 2832829. PMID 17538955. The protein products of jnk1 and jnk2 are believed to be expressed in every cell and tissue type, whereas the JNK3 protein is found primarily in brain and to a lesser extent in heart and testis
  4. ^ Vlahopoulos S, Zoumpourlis VC (August 2004). "JNK: a key modulator of intracellular signaling". Biochemistry Mosc. 69 (8): 844–54. doi:10.1023/B:BIRY.0000040215.02460.45. PMID 15377263. S2CID 39149612.
  5. ^ Oltmanns U, Issa R, Sukkar MB, John M, Chung KF (July 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". Br. J. Pharmacol. 139 (6): 1228–34. doi:10.1038/sj.bjp.0705345. PMC 1573939. PMID 12871843.
  6. ^ Aloyz, R. S.; Bamji, S. X.; Pozniak, C. D.; Toma, J. G.; Atwal, J.; Kaplan, D. R.; Miller, F. D. (1998). "P53 is essential for developmental neuron death as regulated by the TrkA and p75 neurotrophin receptors". The Journal of Cell Biology. 143 (6): 1691–2303. doi:10.1083/jcb.143.6.1691. PMC 2132983. PMID 9852160.
  7. ^ Becker, E. B.; Howell, J.; Kodama, Y.; Barker, P. A.; Bonni, A. (2004). "Characterization of the c-Jun N-terminal kinase-BimEL signaling pathway in neuronal apoptosis". The Journal of Neuroscience. 24 (40): 8762–8770. doi:10.1523/JNEUROSCI.2953-04.2004. PMC 6729963. PMID 15470142.
  8. ^ Liu B, Yip RK, Zhou Z (2012). "Chromatin remodeling, DNA damage repair and aging". Curr. Genomics. 13 (7): 533–47. doi:10.2174/138920212803251373. PMC 3468886. PMID 23633913.
  9. ^ a b c Sellou H, Lebeaupin T, Chapuis C, Smith R, Hegele A, Singh HR, Kozlowski M, Bultmann S, Ladurner AG, Timinszky G, Huet S (2016). "The poly(ADP-ribose)-dependent chromatin remodeler Alc1 induces local chromatin relaxation upon DNA damage". Mol. Biol. Cell. 27 (24): 3791–3799. doi:10.1091/mbc.E16-05-0269. PMC 5170603. PMID 27733626.
  10. ^ a b Van Meter M, Simon M, Tombline G, May A, Morello TD, Hubbard BP, Bredbenner K, Park R, Sinclair DA, Bohr VA, Gorbunova V, Seluanov A (2016). "JNK Phosphorylates SIRT6 to Stimulate DNA Double-Strand Break Repair in Response to Oxidative Stress by Recruiting PARP1 to DNA Breaks". Cell Rep. 16 (10): 2641–50. doi:10.1016/j.celrep.2016.08.006. PMC 5089070. PMID 27568560.
  11. ^ a b Haince JF, McDonald D, Rodrigue A, Déry U, Masson JY, Hendzel MJ, Poirier GG (2008). "PARP1-dependent kinetics of recruitment of MRE11 and NBS1 proteins to multiple DNA damage sites". J. Biol. Chem. 283 (2): 1197–208. doi:10.1074/jbc.M706734200. PMID 18025084.
  12. ^ a b c Calses PC, Dhillon KK, Tucker N, Chi Y, Huang JW, Kawasumi M, Nghiem P, Wang Y, Clurman BE, Jacquemont C, Gafken PR, Sugasawa K, Saijo M, Taniguchi T (2017). "DGCR8 Mediates Repair of UV-Induced DNA Damage Independently of RNA Processing". Cell Rep. 19 (1): 162–174. doi:10.1016/j.celrep.2017.03.021. PMC 5423785. PMID 28380355.
  13. ^ Wang MC, Bohmann D, Jasper H (2003). "JNK signaling confers tolerance to oxidative stress and extends lifespan in Drosophila". Dev. Cell. 5 (5): 811–6. doi:10.1016/s1534-5807(03)00323-x. PMID 14602080.
  14. ^ Wang MC, Bohmann D, Jasper H (2005). "JNK extends life span and limits growth by antagonizing cellular and organism-wide responses to insulin signaling". Cell. 121 (1): 115–25. doi:10.1016/j.cell.2005.02.030. PMID 15820683. S2CID 18365708.
  15. ^ a b Oh SW, Mukhopadhyay A, Svrzikapa N, Jiang F, Davis RJ, Tissenbaum HA (2005). "JNK regulates lifespan in Caenorhabditis elegans by modulating nuclear translocation of forkhead transcription factor/DAF-16". Proc. Natl. Acad. Sci. U.S.A. 102 (12): 4494–9. Bibcode:2005PNAS..102.4494O. doi:10.1073/pnas.0500749102. PMC 555525. PMID 15767565.
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