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Interaction Network for MAPK14

MAPK14 Details

Related Pathways

p38 MAPK Signaling
Xenobiotic Metabolism Signaling
Toll-like Receptor Signaling
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P38 Signaling

Synonyms:CRK1, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Hog, MAPK p38, MAPK14, MGC102436, MGC105413, MXI2, P38, P38 KINASE, P38 Map Kinase, p38 Mapk alpha, P38-ALPHA, p38-RK, p38/Hog1, p38/Mpk2, P38/RK, p38a, p38Hog, p38MAPK, PRKM14, PRKM15, RK, SAPK2A

p38 Signaling

The p38 mitogen-activated protein (MAP) kinase family contains four members: p38 (p38α, p38alpha, CSBP, RK, SAPK2a); p38β (p38beta, SAPK2b); p38γ (p38gamma, ERK6, SAPK3) and p38δ (p38delta, SAPK4). P38 and p38beta are ubiquitous. P38gamma is found predominately in muscle and p38delta is expressed in lung, pancreas, kidney, testis, and small intestine. P38 MAP-kinases all contain the same duel phosphorylation motif, thr-gly-tyr (TGY). The p38 MAP-kinases are activated coordinately by physical-chemical stresses such as: high osmolarity; uv light; or hydrogen peroxide induced oxidative stress; pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), interleukin-1 (IL-1) and TGFbeta (TGFβ) and death receptors (Fas). These stress signals activate a range of MAP3K level kinases such as the RHO-GTPase (Cdc42 and Rac1) downstream effector, p21/Cdc42/Rac1-activated kinase 1 (PAK1); transforming growth factor beta-activated kinase-1 (TAK1) and mitogen-activated protein kinase kinase kinase (ASK1), which in turn activate various MAP2Kinases, the MKKs. P38 alpha, gamma and delta MAPkinase are activated by both MKK3 and MKK6 (SKK3). In addition, p38 is activated along with JNKs by MKK4. P38beta is activated only by MKK6 (SKK3).

The downstream targets of the p38 MAPkinases include a wide array of cytoplasmic and nuclear factors. Key targets include the 90-kDa ribosomal S6 kinase (pp90rsk) (RSK) family: RSK1, RSK2, MNK1/2 and MSK1/2 and nuclear translation factors such as Elk-1, ATF2, STAT3 and CREB. These factors represent only a small number of the p38 substrates. Cellular response to stress activation depends upon the activity of each specific p38 isoform and cell context.


References:

  1. Fearns, C. et. al. (2000) Coordinate activation of endogenous p38alpha, beta, gamma, and delta by inflammatory stimuli. J. Leukoc. Biol. 67, 705-711.
  2. Han, J. et. al. (1994) A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells. Science. 265, 808-811.
  3. Jiang, Y. et. al. (1997) Characterization of the structure and function of the fourth member of p38 group mitogen-activated protein kinases, p38delta. J. Biol. Chem. 272, 30122-30128.
  4. Jiang, Y. et. al. (1996) Characterization of the structure and function of a new mitogen-activated protein kinase (p38beta). J. Biol. Chem. 271, 17920-17926.
  5. Li, Z. et. al. (1996) The primary structure of p38 gamma: a new member of p38 group of MAP kinases. Biochem, Biophys. Res. Commun. 228, 334-340.
  6. Zhang, S. et. al. (1995) Rho family GTPases regulate p38 mitogen-activated protein kinase through the downstream mediator Pak1. J. Biol. Chem. 270(41):23934-23936.

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Content for this page is provided by Dennis R. Conrad, Ph.D., a Life Science industry consultant with over 25 years of experience in the formulation and optimization of cell culture media. Dr. Conrad's email address is biomediaexpert@earthlink.net