MAPK Kinase phosphorylation

E. G protein-conpled receptors /3-Adrenergic receptor kinase (BARK) Rhodopsin kinase II. Ser/Thr/Tyr protein kinases MAP kinase kinase (MAPK kinase) —TEY— phosphorylation by... 

This intermediate MAPK activator (MAPK kinase, MAPKK) is a 45 kDa phosphoprotein capable of phosphorylating MAPK on serine/threonine and tyrosine residues (Matsuda et al., 1992 Nakielny et al., 1992a Kosako et al., 1993). Like MAPK, the activity of MAPKK is regulated by phosphorylation. During oocyte maturation MAPKK is phosphorylated on threonine residues (Kosako et al., 1992), and this phosphorylation is required for its activity (Ahn et al., 1991 Gomez and Cohen, 1991 Kosako et al., 1992 Matsuda et al., 1992). MPF can activate both MAPKK and MAPK in vitro, with the activation of MAPK lagging behind that of MAPKK however, MPF cannot activate either purified MAPKK or MAPK that has been dephosphorylated by phosphatases (Matsuda et al., 1992). MAPKK and MAPK are therefore believed to function downstream of MPF (Fig. 3). 

MAPK kinase (MAPKK). MAPK kinase itself is activated by phosphorylation by still another protein kinase, termed MAPK kinase kinase (MAPKKK). MAPK kinase kinase is activated upon interaction with a member of the Ras superfamily of small G proteins, which are bound to the plasma membrane (see Ch. 19). The exact mechanism of activation remains unknown, but it is believed that Ras and related proteins, in the activated GTP-bound form, can bind MAPK kinase kinase and thereby draw the kinase to the plasmalemma, where it is activated by as yet unknown factors, perhaps even an additional kinase, MAPK kinase kinase kinase (MAPKKKK). The mechanism governing the activation of Ras and related proteins by extracellular signals is quite complex and involves numerous Tinker proteins, for example She, Grb and Sos, that couple Ras to a variety of plasmalemma-associated growth factor-protein tyrosine kinase receptors (see Chs 20,24 and 27). 

A second family of MAPKs is referred to as stress-activated protein kinases (SAPKs) [3,14,15]. This includes JNKs, or Jun kinases, named originally for their phosphorylation of the transcription factor c-Jun. SAPKs were first identified in peripheral tissues on the basis of their activation in response to cellular forms of stress, which include X-ray irradiation and osmotic stress. More recently, they have been demonstrated to be activated in brain by several cytokines as well as by synaptic activity [16]. As shown in Figure 23-3, SAPKs are activated by SAPK kinases (SEKs), which are in turn activated by SEK kinases. The Ras-like small G proteins implicated in SEK kinase activation are Rac and Cdc-42. In this case, it appears that Rac/Cdc-42 triggers activation of SEK kinase by stimulating its phosphorylation by still another protein kinase termed p21-activated kinase (PAK). Thus, PAK can be considered a MAPK kinase kinase kinase, which is analogous to the cascade of protein kinases found in yeast (Fig. 23-4). 

Mitogen-activated protein kinase phosphatases are dual-function protein phosphatases. Just as the MAPK kinases (e.g. MEKs) are unique as dual-functioning kinases in that they phosphorylate MAPKs on threonine and tyrosine residues, there are unique dual-function ing protein phosphatases that reverse the phosphorylation and activation of MAPKs [43], Such MAPK phosphatases (MKPs) were first identified as a product of vaccinia virus (VH1) and later found in all eukaryotic cells. There are now numerous members of this VH1 family of dual-functioning protein phosphatases. 

The MEK kinases (MAPKK kinases) are Ser/Thr-specific protein kinases and are the entry point for signal transduction in a MAPK module. The best characterized representative, Raf-1 kinase, is activated by Ras protein in its GTP-bound form. Raf kinase phosphorylates downstream MEK proteins at two Ser residues, which are separated by three other amino acids. All known MEK proteins have a similar phosphorylation site in the conserved sequence LID/NSXANS/T (X any amino acid). Other representatives of the MEK kinase group are Mos kinase and the protein kinases MEKKl—3. 

Fig. 10.2. Components and activation of the ERK pathway. Ordering and specificity of protein kinases in the ERK pathway. ExtraceUular signals are registered via receptor tyrosine kinases and passed on to the Ras protein. Ras GTP activates protein kinases belonging to the group of MAPKK kinases (Raf kinases and MEEKs). The MAPKK kinases phosphorylate the downstream group of protein kinases, the MAPKKs at two Ser residues. The MAPKKs phosphorylate the MAPKs (ERKl and ERK2) at a Tyr and a Thr residue, and thus are classified as dual specificity kinases. MAPK mitogenic activated protein kinase ERK extracellularly regulated kinase MEK MAP/ERK kinase MAPKK MAPK kinase MAPKKK MAPKK kinase MEKK MEK kinase.

Many of the signaling protein kinases, including PKA, PKC, PKG, and members of the MAPK cascade, phosphorylate Ser or Thr residues in their target proteins, which in some cases acquire the ability to interact with partner proteins through the phosphorylated residue, triggering a downstream process. An alphabet soup of domains that bind (P)-Ser or (P)-Thr residues has been identified, and more are sure to be found. Each domain favors a certain sequence around the phosphorylated residue, so the domains represent families of highly specific recognition sites, able to bind to a specific subset of phosphorylated proteins. 

If we concentrate on one particular component of this map - the phosphorylation of PI(4,5)P2 to PI(3,4,5)P3 by PI3K and the dephosphorylation of PI(3,4,5)P3 to PI(4,5)P2 by F TEN, we can study the detailed enzyme kinetic scheme of this so-called phosphorylation-dephosphorylation cycle, which is illustrated in Figure 5.2. This illustrated cycle represents a ubiquitous module in biochemical signaling, ft could, for example, represent the phosphorylation of mitogen-activation protein kinase (MAPK) by MAPK kinase (MAPKK) and dephosphorylation of MAPK by MAPK phosphatase (MKP). 

A discrete region of 40 residues in the amino-terminal part of p38 MAPK is mainly responsible for screening of extracellular signals, transmitted by the upstream kinases, whereas the carboxy-terminal half of the AlAPK binds to downstream substrates, such as transcription factors. The amino-terminal recognition region of the MAPK contains an exposed a-helix in the proximity of the catalytic cleft, which is the phosphorylation site recognized by an upstream kinase. Phosphorylation opens the catalytic cleft and activates the kinase. This seems to be a common structural feature of kinases participating in sequential reactions in phosphorylation cascades. 

Substrate recognition and selection of the JNK/SAPK and p38 proteins (and also the ERK proteins) are mediated both by specific docking sites and by the nature of the amino acids surrounding the phosphoacceptor site. For the transcription factor substrates, specific docking domains have been identified that are loacted at a distance from the phosphorylation sites in the transactivation domain. These docking sites serve to increase the selectivity and specificity of phosphorylation, and they are used for recruitment of MAPK kinases into protein complexes at promotors, where they can phosphorylate other regulatory transcriptional proteins. 

MAPK is activated by a unique dual function kinase called MEK, which is an acronym for MAPK and ERK-kinase (Crews et al, 1992 Zheng and Guan, 1993). MEK has also been named MAPK-kinase (or MAPKK) and is unusual because it phosphorylates MAPK on both a threonine and a tyrosine amino acid. MEK consists of a family of at least three protein kinase isoforms, each of which shows differential reactivity toward the different members of the MAPK family. Each MEK isoform is activated through phosphorylation mechanisms. When fully dephosphorylated, MEK is inactive. When phosphorylated by either MEK-kinase (MEKK) or the proto-oncogene raf, the phosphotransferase activity of MEK is "turned on." Although both raf and MEKK can activate MEK, differential activation of either of these kinases can lead to the activation of different downstream signal transduction pathways. Therefore, the roles of raf and MEKK in the cell are not limited to MEK and, therefore, MAPK activation. 

---