The MAPK/ERK pathway is a signal transduction pathway that couples intracellular responses to the binding of growth factors to cell surface receptors. This pathway is very complex and includes many protein components [ R. J. Orton, O. E. Sturm, V. Vyshemirsky, M. Calder, D. R. Gilbert and W. Kolch (2005) "Computational modelling of the receptor-tyrosine-kinase-activated MAPK pathway" in The Biochemical journal Volume 392, pages 249-261. Review..]. The basic pathway shown in the figure (to the right) and described below includes the major components of the pathway. In many cell types, activation of this pathway promotes cell division.
Coupling cell surface receptors to G proteins
Receptor-linked
tyrosine kinases such as the
epidermal growth factor receptor (EGFR) are activated by extracellular
ligands. Binding of epidermal growth factor (EGF) to the EGFR activates the tyrosine kinase activity of the cytoplasmic domain of the receptor. The EGFR becomes
phosphorylated on tyrosines. Docking proteins such as
GRB2 contain
SH2 domains that bind to the phosphotyrosines of the activated receptor
[ W. X. Schulze, L. Deng and M. Mann (2005) "Phosphotyrosine interactome of the ErbB-receptor kinase family" in Molecular systems biology Volume 1, May 25..]. GRB2 binds to the
guanine nucleotide exchange factor SOS by way of an
SH3 domain of GRB2. When the GRB2-SOS complex docks to phosphorylated EGFR, SOS becomes activated
[ N. Zarich, J. L. Oliva, N. Martinez, R. Jorge, A. Ballester, S. Gutierrez-Eisman, S. Garcia-Vargas and J. N. Rojas (2006) "Grb2 Is a Negative Modulator of the Intrinsic Ras-GEF Activity of hSos1" in Molecular Biology of the Cell Epub ahead of print..]. Activated SOS promotes the removal of
GDP from
Ras. Ras can then bind
GTP and become active. Other
small G proteins can be activated in a similar way, but are not discussed further here.
Kinase cascade
Activated Ras activates the protein kinase activity of
RAF kinase
[J. Avruch, A. Khokhlatchev, J. M. Kyriakis, Z. Luo, G. Tzivion, D. Vavvas and X. F. Zhang (2001) "Ras activation of the Raf kinase: tyrosine kinase recruitment of the MAP kinase cascade" in Recent Progress in Hormone Research Volume 56, pages 127-155. .], a serine/threonine-selective
protein kinase. RAF kinase phosphorylates and activates MEK, another serine/threonine kinase. MEK phosphorylates and activates
mitogen-activated protein kinase (MAPK).
Technically, RAF, MEK and MAPK are all mitogen-activated kinases, as is MNK (see below). MAPK was originally called "extracelular signal-regulated kinase" (ERK) and microtubule-associated protein kinase (MAPK). One of the first proteins known to be phosphorylated by ERK was a microtubule-associated protein. As discussed below, many additional targets for phosphyrylation by MAPK were later found and the protein was re-named "mitogen-activated protein kinase" (MAPK). The series of kinases from RAF to MEK to MAPK is an example of a protein kinase cascade. Such series of kinases provide opportunities for feedback regulation and signal amplification.
Regulation of translation and transcription
Three of the many proteins that are phosphorylated by MAPK are shown in the Figure. One effect of MAPK activation is to alter the
translation of
mRNA to proteins. MAPK phosphorylates 40S
ribosomal protein S6 kinase (RSK). This activates RSK which in turn phosphorylates ribosomal protein S6
[M. Pende, S. H. Um, V. Mieulet, M. Sticker, V. L. Goss, J. Mestan, M. Mueller, S. Fumagalli, S. C. Kozma and G. Thomas.(2004) "S6K1,(-/-)/S6K2(-/-) mice exhibit perinatal lethality and rapamycin-sensitive 5'-terminal oligopyrimidine mRNA translation and reveal a mitogen-activated protein kinase-dependent S6 kinase pathway" in Molecular and Cellular Biology Volume 24, pages 3112-3124. .]. Mitogen-activated protein kinases that phosphorylate ribosomal protein S6 were the first to be isolated
.
MAPK regulates the activities of several transcription factors. MAPK can phosphorylate C-myc. MAPK phosphorylates and activates MNK which in turn phosphorylates CREB. MAPK also regulates the transcription of the Fos gene. By altering the levels and activities of transcription factors, MAPK leads to altered transcription of genes that are important for the cell cycle.
See also
External links
References
Signal transduction | Cell signaling