Vol. 14, No. 9, pp. 1027-1047, May 1, 2000

REVIEW
Protein-protein interactions define specificity in signal transduction

Program in Molecular Biology and Cancer, Samuel Lunenfeld Research Institute, Mt. Sinai Hospital, Toronto, Ontario M5G 1X5, Canada

	Introduction

Top Introduction Specificity and complexity at... Specific activation of... Multiple modules in signal... Generality of protein-protein... Specificity in signaling by... Scaffolding and docking... Guidance receptors and... Integration of signaling... Evolution of signaling pathways Regulating the intensity of... Conclusions References

Virtually every aspect of cellular function within a metazoan organism, including proliferative status, metabolism, gene expression, cytoskeletal organization, and indeed the cell's very survival, is dependent on external signaling molecules, either in the form of soluble hormones or proteins anchored to the surface of an adjacent cell or the extracellular matrix (ECM). These factors exert their effects either by binding receptors displayed on the surface of the cell or, in the case of compounds such as steroids, by traversing the plasma membrane and directly engaging intracellular receptors. In addition, these external signals can be linked to intrinsic cues that regulate events such as polarity and asymmetric cell division, and that monitor the molecular composition of the cell, and therefore determine whether suitable conditions prevail for cell growth and division.

Over the last two decades, we have achieved considerable understanding of the mechanisms by which signals are conveyed from receptors at the plasma membrane to their targets in the cytoplasm and nucleus. At heart, this is a problem of molecular recognition. Hormones must bind selectively to their receptors and these in turn must interact with specific cytoplasmic targets. To understand signal transduction in a general sense, it is important to know whether different biochemical pathways use related molecular devices to control cellular behavior. To understand specificity in signaling, we need to know how receptors interact with particular targets and how the proteins of one pathway can be insulated from related signaling components. At the same time, it is important to learn how distinct signaling pathways communicate with one another, since the entire cell must ultimately function as a single unit whose different elements respond in an organized fashion to external signals. A cell in the body will be exposed to many different stimuli, which it must integrate into a coherent response.

Furthermore, although a rather large fraction of genes within nucleated cells appear to function in the processes of signal transduction and cellular organization (Plowman et al. 1999), it is still remarkable that only a few thousand gene products can control the sophisticated behaviors of many different cell types. This immediately suggests that signaling proteins must act in a combinatorial fashion, since there are insufficient proteins for each to have a single biological role. For example, there are billions of neurons in the human brain, each of which must project its axon to the appropriate target, let alone undertake the complex biochemical events associated with neurotransmission and synaptic plasticity. Clearly, the signaling molecules that function in the process of axon guidance must act in a combinatorial way to generate the extreme complexity of the human nervous system.

Here we will address some of the underlying biochemical mechanisms through which specificity is generated during signal transduction, and pursue the means by which signaling molecules may act in combination to generate complex biological responses.

	Specificity and complexity at the level of receptors

Top Introduction Specificity and complexity at... Specific activation of... Multiple modules in signal... Generality of protein-protein... Specificity in signaling by... Scaffolding and docking... Guidance receptors and... Integration of signaling... Evolution of signaling pathways Regulating the intensity of... Conclusions References

The mechanisms of receptor activation have been intensively studied through the analysis of receptor tyrosine kinases (RTKs), which possess a single membrane-spanning region, and related multisubunit receptors, such as those for cytokines and antigens that signal through associated cytoplasmic tyrosine kinases (Hunter 2000). The binding of a hormone to such receptors induces either receptor oligomerization (Heldin et al. 1995; Plotnikov et al. 1999) or the spatial reorientation of preclustered chains, as shown for the erythropoietin receptor (Remy et al. 1999). As a consequence, ligand binding to a RTK promotes the intermolecular autophosphorylation of one receptor chain by its neighbor, usually within the activation segment of the kinase domain (Hubbard 1997). This results in displacement of the activation segment from the active site. The stimulated kinase domain then phosphorylates additional tyrosine residues, usually within noncatalytic regions of the receptor, which provide docking sites for downstream targets.

The exclusive binding of a single growth factor to an individual receptor is more likely the exception than the rule. Indeed, the oligomeric nature of activated receptors allows the formation of receptor complexes composed of distinct, albeit closely related subunits, which can have different signaling potentials (Pinkas-Kramarski et al. 1998). As a simple example, platelet-derived growth factor (PDGF) is a covalently linked dimer composed of A or B chains in different combinations, which induces the formation of a receptor dimer similarly composed of  or  chains (Heldin et al. 1998). Because the B chain of PDGF only binds the  receptor, whereas both A and B PDGF bind the  receptor, different dimeric forms of PDGF induce distinct combinations of receptor chains. Interestingly, the signaling properties of the  and  receptor chains differ from one another, since the / PDGF receptor heterodimer is more potent in stimulating mitogenesis that either of the homomeric receptors. This correlates with a failure of the / receptor to bind Ras GTPase activating protein, a negative regulator of the Ras GTPase, resulting in enhanced activation of the Ras-MAP kinase (MAPK) pathway (Ekman et al. 1999).

Yet more diversity can be seen in the four members of the ErbB RTK family, which bind several ligands, including epidermal growth factor (EGF) and the neuregulins (NRG). Although all possible dimeric combinations of receptors can form, ErbB2, which itself does not bind ligands with high affinity, is a preferred heterodimeric partner (Pinkas-Kramarski et al. 1998). A biological requirement for heterodimer formation is revealed by the observation that mutations in the ErbB2 and ErbB4 receptors, and the NRG-1 ligand, give essentially identical phenotypes in mouse embryos (Gassmann et al. 1995; Lee et al. 1995; Meyer and Birchmeier 1995). Different receptor chains have distinct cytoplasmic binding sites for intracellular signaling proteins and as a result give distinct signaling outputs, as measured by the strength of MAPK activation. Of interest, ErbB3 lacks intrinsic catalytic activity, but is trans-phosphorylated by a kinase-active partner such as ErbB2, and thus serves a scaffolding function through its ability to bind cyotplasmic targets. Indeed, the ErbB2/ErbB3 heterodimer is potently mitogenic (Waterman et al. 1999).

It is common for a single receptor to bind and be activated by more than one extracellular ligand. For example, the prolactin cytokine receptor can engage both growth hormone and prolactin. Structural and mutagenesis analysis has indicated that the ligand-binding sites of cell surface receptors may be rather adaptable, composed of relatively hydrophobic yet solvent accessible surfaces (Cunningham and Wells 1991; Lowman et al. 1991). Although the ligand-binding surfaces are quite large, only a few residues are critical for ligand recognition. In the example cited above, the two hormones recognize overlapping sites on the same receptor, but are dependent on distinct residues for high affinity binding. Such data suggest that receptors combine selectivity for specific ligands with the potential for flexibility and possibility for rapid evolution of hormone recognition. As discussed below, protein-protein interactions within the cell that control cytoplasmic signaling pathways display many of the same characteristics.

In addition to the formation of multichain receptors through the interactions of distinct subunits, recent data suggest that entirely different receptors may directly interact with one another at the surface of the same cell. This leads to the possibility of cross-talk between separate receptors and pathways at the very earliest steps in signaling. In the nervous system, the  chain of the heteropentameric GABA_A receptor, which is a ligand-gated ion channel, physically interacts through a cytoplasmic loop with the carboxy-terminal region of the dopamine D5 receptor, a seven transmembrane-spanning G protein-coupled receptor (GPCR) that links to Gs and the production of cAMP (Liu et al. 2000). This association leads to a mutual inhibition of the two receptors and provides a mechanism through which a GPCR may influence synaptic strength independently of G protein signaling. Similarly, neurotrophins acting through Trk family RTKs can rapidly induce action potentials in CNS neurons, suggesting that Trk receptors may interact with a Na⁺ channel (Kaffitz et al. 1999). These types of interaction are not confined to the nervous system. For example, the Kit RTK, which is activated by the hematopoietic stem cell factor, can bind and phosphorylate the cytoplasmic region of the erythropoietin cytokine receptor (Wu et al. 1995).

	Specific activation of signaling pathwaysprotein domains and motif recognition

Top Introduction Specificity and complexity at... Specific activation of... Multiple modules in signal... Generality of protein-protein... Specificity in signaling by... Scaffolding and docking... Guidance receptors and... Integration of signaling... Evolution of signaling pathways Regulating the intensity of... Conclusions References

The involvement of modular protein-protein interactions in signaling from cell surface receptors was originally recognized in the context of RTKs. As noted above, receptor activation leads to the intermolecular phosphorylation of receptor chains at sites that consequently bind proteins with SH2 domains (Pawson 1995; Kuriyan and Cowburn 1997). SH2 domains are protein modules of ~100 amino acids that recognize phosphotyrosine residue-containing peptides in the context of 3-6 carboxy-terminal amino acids (Eck et al. 1993; Waksman et al. 1993; Pascal et al. 1994). As with many interaction modules, the amino and carboxyl termini of SH2 domains are close together in space, and on the opposite face from the ligand-binding surface. This potentially allows an SH2 domain to be inserted into a host protein at an internal location, while leaving the phosphopeptide-binding surface free to engage ligands. Most SH2 domains require phosphorylation of the peptide ligand for high affinity binding, but differ in their ability to recognize residues carboxy-terminal to the pTyr, thereby imbuing each SH2 domain with an ability to bind preferentially to a specific phosphorylated motif (Songyang et al. 1993). Thus, in the case of activated RTKs, their ability to stimulate cytoplasmic signaling pathways is to some extent determined by the sequence contexts of their autophosphorylation sites, which in turn dictates which SH2-containing proteins will engage the autophosphorylated receptor.

SH2 domains must therefore achieve something of a balancing act. Their affinity for an unphosphorylated site must not be too high, or binding could not be regulated by phosphorylation, yet they must gain sufficient binding energy from the recognition of more carboxy-terminal residues to allow discrimination between different sites. Furthermore, their off-rates must be sufficiently high to allow for rapid signal transduction. Perhaps for this reason the interactions of SH2 domains with phosphopeptide motifs can be highly dynamic (Kay et al. 1998). For example, although the SH2 domains of phospholipase C (PLC)-1 and the Shp2 tyrosine phosphatase both bind pTyr followed by five hydrophobic residues, the PLC-1 SH2-C domain obtains more binding energy from electrostatic interactions involving the pTyr, whereas the Shp2 SH2-N domain has larger contributions from the hydrophobic interface. Strikingly, although the PLC-1 SH2 domains show strong selectivity at the +1 to +5 positions, the SH2 domain residues lining the hydrophobic groove that accommodates these amino acids show significant motional disorder even following ligand binding. This leads to the possibility that SH2 domain binding specificity results from a combination of permissive and inhibitory forces. Thus compatible residues in the SH2 domain and ligand will promote binding, whereas residues that sterically interfere with phosphopeptide recognition will inhibit recognition. Consistent with this view, the SH2 domains of PLC-1 can potentially bind a site with a pYXXM motif, that normally accommodates phosphatidylinositol 3'-kinase (PI3K), but are excluded from such a site by a Ser at the +4 position, as found in physiological PI3K-binding sites on the PDGF receptor (Larose et al. 1995).

The potential flexibility of SH2 domains is emphasized by the ability of single amino acid substitutions to alter binding specificity (Fig. 1). SH2 domains generally fall into three classes: PLC--like SH2 domains bind phosphopeptides as an extended strand, with carboxy-terminal residues fitting into a hydrophobic cleft. Src-like SH2 domains are similar, but have a flat binding surface that selects for charged residues at the +1 and +2 positions, while the sidechain of the +3 residue fits into a hydrophobic pocket. In contrast, the Grb2 SH2 domain has a bulky Trp sidechain that blocks the progress of the phosphopeptide ligand, which is forced into a  turn, best accommodated by a +2 Asn. Surprisingly, it is possible to convert a PLC- SH2 domain to a Src-like specificity by changing a single Cys residue (at the D5 position) to Tyr (Songyang et al. 1995). Similarly the Src SH2 domain can be converted to a Grb2-like specificity by altering a Thr (at the EF1 site) to Trp. This mutant Src SH2 domain mimics Grb2 at the structural level, and functions in Caenorhabditis elegans development as if it were a Grb2 SH2 domain (Marengere et al. 1994). This apparent flexibility may have an evolutionary advantage, in the sense that SH2 domain binding specificity might change rather rapidly, allowing the formation of new signaling connections as metazoan organisms became more complex.

View larger version (100K): [in this window] [in a new window]   Figure 1.   Evolution of SH2 domain-binding specificity. The surfaces of the PLC-1, Src, and Grb2 SH2 domains are shown in blue, with their corresponding peptide ligands (pYIIPLPD, pYEEI, pYVNV, respectively) shown in yellow. In each case the pTyr is to the right. For PLC-1, the +1 Ile of the ligand fits into the start of a hydrophobic groove, framed by a Cys (D5) shown in green. In the Src SH2 domain this Cys is replaced by a Tyr (in green) which makes a flat surface that selects for charged residues in the +1 and +2 positions. Src has a pocket that accommodates the hydrophobic side chain of the +3 Ile, which is formed in part by a Thr (EF1) shown in red. In the Grb2 SH2 domain this Thr is replaced by a Trp (in red) which fills up the pocket and forces the phosphpeptide into a -turn. Changing the Cys in PLC-1 to Tyr converts the PLC-1 SH2 domain to a Src-like specificity, and conversely changing the Thr in Src to Trp results in a Grb2-like specificity.

The relevance of specific SH2 domain-mediated interactions to biological signaling pathways has also been tested by introducing mutations into SH2 docking sites on receptors. A nice example is provided by the EGF receptor homolog in C. elegans, LET-23, which is required for vuval differentiation, viability and ovulation (Lesa and Sternberg 1997). LET-23 has eight potential autophosphorylation sites within its carboxy-terminal tail, with binding motifs for SH2 proteins such as Grb2, PLC-, and SLI-1 (the worm homolog of mammalian c-Cbl). The three carboxy-terminal autophosphorylation sites (Y6-8) lie in YXN motifs that can bind the worm Grb2 adaptor and thereby activate the Ras pathway. These sites have a redundant role in vulval formation and viability but are not required for ovulation. In contrast, the Y5 site, which likely signals through PLC- to activate the inositol triphosphate (IP₃)-receptor and elevate intracellular calcium, has a unique role in ovulation. Furthermore, the Y2 site inhibits LET-23 signaling, potentially through the SLI-1/c-Cbl SH2 protein, which likely acts as an E3 protein-ubiquitin ligase (Joazerio et al. 1999).

In the mammalian system, the Met receptor tyrosine kinase has two closely spaced Tyr phosphorylation sites within its carboxy-terminal tail, that bind a number of SH2-containing proteins. Substitution of both Tyr residues with Phe in the mouse causes embryonic lethality similar to that seen with a null allele, suggesting that although the receptor retains kinase activity, it is functionally impotent when stripped of its SH2-docking sites (Maina et al. 1996). In contrast, a Met receptor with a more subtle substitution that alters a +2 Asn crucial for Grb2-binding has a milder phenotype, involving defects in muscle development. Similarly, substitution of Tyr 719 in the mouse Kit RTK, that normally engages PI3K, impairs specific aspects of Kit function required for the survival of male germ cells (Blume-Jensen et al. 2000), and ovarian follicle development (Kissel et al. 2000). However, PI3K-binding is not significantly required for Kit's role in melanogenesis and hematopoiesis. In a similar vein, substitutions of the PI3K binding sites (Tyr 739/750) in the mouse PDGF receptor cause a very subtle phenotype, resulting in decreased chemotaxis and ability to contract a collagen gel in culture, and a failure to normalize interstitial fluid pressure in vivo (Heuchel et al. 1999). These data are consistent with the view that individual receptor phosphorylation sites bind SH2 signaling proteins in a sequence-dependent manner, resulting in the activation of defined biochemical pathways and specific biological responses.

There are a number of complications to this simple view. First, different signaling pathways may ultimately converge on overlapping targets, and thus have partially redundant functions (Fambrough et al. 1999). Second, some signaling pathways may have subtle biological activities. Furthermore, some RTKs can phosphorylate specific docking proteins at residues that subsequently bind SH2 proteins, and provide signaling activity even in the absence of SH2-binding sites on the receptor itself. Examples include the Shc, IRS-1, and FRS2 proteins. These characteristically possess a means of membrane attachment, a receptor-binding PTB domain, and multiple sites for tyrosine phosphorylation and SH2-binding (Sun et al. 1993; van der Geer et al. 1996; Kouhara et al. 1997).

It is instructive to consider how these docking proteins are recruited to activated receptors. Their PTB domains specifically recognize pTyr-containing motifs, although in an entirely different way from SH2 domains (Zhou et al. 1995), and preferentially bind phosphorylated NPXY elements in the receptor's juxtamembrane region (Trub et al. 1995; van der Geer et al. 1995). Interestingly, a growing number of proteins have been found to possess PTB domains that bind NPXY, or related, motifs but do not require phosphorylation for high affinity binding (Borg et al. 1998). This has led to the notion that PTB domains originally evolved to recognize non-phosphorylated peptide motifs, and subsequently developed a capacity for pTyr-binding in specific cases. Indeed, the PTB domain of FRS2 binds both to a phosphorylated NPXY site on the activated TrkA neurotrophin receptor, and to an entirely different non-phosphorylated site on the FGF-receptor (Ong et al. 2000) (Fig. 2). Rather strikingly, PTB domains have a similar structural fold to PH domains (which bind phospholipids) and EVH1 domains (which bind proline-rich motifs), as well as to a protein that binds the Ran GTPase, suggesting that this is a rather versatile scaffold that has been exploited for several different protein and phospholipid recognition events (Yoon et al. 1994; Prehoda et al. 1999; Vetter et al. 1999).

What purpose is served by docking proteins that associate with RTKs? One possibility is that they amplify signaling from a given receptor to a particular biochemical pathway. Phosphorylation of IRS-1 by the insulin receptor creates multiple binding sites for PI3K, whereas Shc and FRS2 primarily engage Grb2, and thus are principally involved in activating the MAPK pathway. Another role for a docking protein may be to juxtapose cytoplasmic proteins that act at successive stages of a pathway. An example is provided by the SLP-76 protein that functions downstream of the T-cell antigen receptor. SLP-76 is an SH2 protein that is recruited to the T-cell receptor target LAT through an SH2/SH3 adaptor protein, GADS. SLP-76 is then phosphorylated at multiple sites by the receptor-associated kinase ZAP-70, and consequently binds SH2 proteins (Liu et al. 1999). One such binding protein is Vav, which acts as a guanine nucleotide exchange factor (GEF) to activate the Rac GTPase. SLP-76 also binds the SH2/SH3 adaptor Nck, which complexes through its SH3 domains with the serine/threonine kinase Pak. Pak is activated by GTP-bound Rac (produced by Vav) and induces cytoskeletal re-organization. SLP-76 therefore functions as a scaffold that juxtaposes members of a pathway targeting the cytoskeleton (Bubeck Wardenburg et al. 1998).

	Multiple modules in signal transduction

Top Introduction Specificity and complexity at... Specific activation of... Multiple modules in signal... Generality of protein-protein... Specificity in signaling by... Scaffolding and docking... Guidance receptors and... Integration of signaling... Evolution of signaling pathways Regulating the intensity of... Conclusions References

SH2 domains serve as a prototype for a large and growing family of modular protein domains found in intracellular signaling proteins (see http://smart.embl-heidelberg.de/) (Schultz et al. 2000). In addition to domains involved in the recognition of pTyr- and pSer/Thr-containing peptides, there are a series of modules that recognize specific proline-rich peptide motifs, including SH3, WW, and EVH1 domains (Niebuhr et al. 1997; Nguyen et al. 1998; Aghazadeh and Rosen 1999). EH domains recognize Asn-Pro-Phe sequences, commonly found in polypeptides involved in protein trafficking (Salcini et al. 1997; Mayer 1999), whereas PDZ domains bind short peptide motifs at the extreme carboxyl termini of proteins, typically transmembrane receptors (Songyang et al. 1997). Two folded PDZ domains can also bind directly to one another (Hillier et al. 1999), and SAM domains also appear to have an intrinsic capacity to undergo self-oligomerization (Stapleton et al. 1999; Thanos et al. 1999). As well as modules involved in domain-peptide or domain-domain interactions, there are several examples of domains that bind selectively to phospholipids and thereby target proteins to specific sites in the membrane to directly regulate their activity or access to substrates. In particular, FYVE domains frequently bind specific phosphoinositides, and therefore thereby mediate the effects of PI kinases on cellular behaviour (Fruman et al. 1999; Rameh and Cantley 1999). Recent evidence suggests that the homodimerization of PH and FYVE domains may increase the avidity with which they bind membrane sites (Mao et al. 2000).

In many cases, cytoplasmic signaling proteins possess multiple protein-protein and protein-phospholipid interaction domains, covalently linked in various combinations. The joining of different domains can serve a variety of functions. Two domains may interact with different sites on the same target, as commonly occurs with polypeptides that possess tandem SH2 domains, thereby increasing both the affinity and specificity of the interaction (Ottinger et al. 1998). Conversely, separate domains may interact with distinct partners, as observed for adaptors with SH2 and SH3 domains, such as Grb2 that links activated receptors to downstream targets with proline-rich motifs, notably the Ras GEF Sos1 (Li et al. 1993; Rozakis-Adcock et al. 1993) (Fig. 2). Furthermore, modular domains can engage in complex intramolecular interactions that regulate the enzymatic activities of their host protein, as occurs in the Src family kinases or the Shp2 tyrosine phosphatase (Sicheri et al. 1997; Xu et al. 1997; Hof et al. 1998). These roles are not necessarily mutually exclusive. In the Src tyrosine kinase, phosphorylation of a carboxy-terminal tyrosine leads to intramolecular interactions in which the SH2 and SH3 domains engage internal ligands and block kinase activity. However, once these intramolecular interactions are broken, the SH3 and SH2 domains play an important role in tethering Src to its substrates and in promoting processive phosphorylation (Sakai et al. 1994; Pellicena et al. 1998).

View larger version (46K): [in this window] [in a new window]   Figure 2.   Modular protein-protein interaction domains convey signals from activated receptors using a variety of recognition motifs. Both the TNF and FGF receptors employ modular protein-protein interaction domains to convey signals. The activated TNF-R1 trimer binds a docking protein, TRADD, through death domain (DD)-DD interactions. TRAD, in turn, binds to a variety of adaptors, including FADD, TRAFs, and RIP. FADD recruits procaspase 8, which initiates a proteolytic cascade resulting in apoptosis. Recruitment of TRAF-2 via the TRAF-C domain initiates the Jnk pathway, whereas recruitment of RIP activates NFB signaling. In an analogous manner, the FGF-R is clustered by FGF and proteoglycan. The myristoylated FRS2 scaffold protein binds to the FGF-R through its PTB domain, becomes phosphorylated on multiple tyrosines, and consequently binds the SH2 proteins Grb2 and Shp2. The Grb2 adaptor recruits Sos1 through its SH3 domain, and Sos1 acts as a GEF for the Ras GTPase. Activated Ras can potentially stimulate multiple pathways to promote cell survival, activate transcription, or cause cytoskeletal rearrangement.

	Generality of protein-protein interactions in signaling

Top Introduction Specificity and complexity at... Specific activation of... Multiple modules in signal... Generality of protein-protein... Specificity in signaling by... Scaffolding and docking... Guidance receptors and... Integration of signaling... Evolution of signaling pathways Regulating the intensity of... Conclusions References

TGF receptors

The process through which protein-protein interactions mediate phosphotyrosine signaling represents a specific aspect of a more general process in signal transduction. Members of the TGF receptor family exert their effects through type 1 and type II receptors with protein serine/threonine kinase activity (Massague 1998). Binding of TGF causes the type II receptor to phosphorylate the type I receptor, which is thereby induced to phosphorylate downstream targets, the regulated (R-) Smads, at three carboxy-terminal sites within an SSXS motif. The Smad proteins have an amino-terminal MH1 domain, a central linker, and a carboxy-terminal MH2 domain, which recognizes the type I receptor. R-Smad phosphorylation appears to block an internal interaction between the MH1 and MH2 domains, and free the MH2 domain to associate with the so-called common Smad (Smad4), which is not itself phosphorylated. A binding site has been identified on Smad4 that may serve as a receptor for phosphorylated residues of R-Smads (Qin et al. 1999) The resulting R-Smad/Smad4 hetero-oligomeric complex is retained in the nucleus, where it binds to specific promoters through the MH1 domain and to additional transcription factors such as FAST (Wrana 2000) (Fig. 3).

View larger version (48K): [in this window] [in a new window]   Figure 3.   Stats and Smads: Linking receptors to transcription. IFN receptor activation induces protein-tyrosine kinases of the Jak family. These act on the cytoplasmic tail of the receptor, creating SH2 docking sites. STAT proteins are recruited to the membrane via their SH2 domain, and are themselves phosphorylated by the Jak kinases. Phosphorylated STATs dimerize and translocate to the nucleus where they activate transcription by binding directly to specific DNA sequences. In a somewhat anlogous manner, R-SMADs are recruited to activated TGF receptors from their membrane anchor protein SARA. Following phosphoylation, the R-SMAD protein forms heterodimers with SMAD4 and translocates to the nucleus.

There are a number of additional regulatory steps that likely contribute to biochemical and biological specificity in TGF signaling. First, a docking protein termed SARA binds the MH2 domain of unphosphorylated Smad2 and Smad3 and appears to colocalize with the TGF receptor (Tsukazaki et al. 1998; Wu et al. 2000). SARA thereby enhances TGF signaling by increasing the specificity and efficiency with which the receptor phosphorylates its targets. Phosphorylated Smads are released from their SARA anchor. Interestingly, in addition to the Smad-binding region, SARA has a FYVE domain that recognizes PI-3-P, and may therefore direct the Smad to a particular membrane site where it encounters the receptor.

Although there are many differences in the details between RTK and TGF receptor signaling, there are also a number of parallels. The receptor targets are modular and they form complexes with their receptors. In both cases, phosphorylation regulates protein-protein interactions, although in distinct ways. In addition, both RTKs and TGF-receptors can employ docking proteins with phospholipid- and protein-interaction domains, that aid in the recruitment of targets to the receptor. Indeed, the regulation of Smad signaling is somewhat reminiscent of Stats, SH2-containing proteins that function downstream of cytokine receptors to control gene expression (Darnell 1997) (Fig. 3). Stats bind to specific sites on activated cytokine receptors through their SH2 domain, and themselves become phosphorylated, resulting in a mutual SH2-pTyr interaction between two Stat molecules (Chen et al. 1998). The phosphorylated Stats consequently dimerize, are displaced from the receptor, relocate to the nucleus and bind to specific promoters.

There are also similarities in the way that RTK and TGF receptor signaling pathways are inhibited. As noted above, RTKs such as the PDGF receptor can bind the SH2-containing protein c-Cbl, which acts as an E3 protein-ubiquitin ligase to label the receptor for degradation. Within their linker region, Smads have proline-rich (PY) motifs that bind the WW domains of another E3 protein-ubiquitin ligase (Smurf) with a Hect catalytic domain, leading to Smad ubiquitination and destruction (Zhu et al. 1999). Thus in both cases modular protein interactions target specific components of the signaling pathway for degradation, in a fashion that appears critical for appropriate biological responses.

TNF receptor signaling

Members of the tumor necrosis factor (TNF) receptor family lack catalytic domains, but use specific protein-protein interactions to convey signals from the receptor to their downstream targets. A relatively simple example involves the Fas receptor, which induces cell death upon stimulation with the Fas-ligand (Ashkenazi and Dixit 1998). Fas has a carboxy-terminal death domain (DD), which interacts specifically with a related DD at the carboxyl terminus of the adaptor protein FADD (Chinnaiyan et al. 1995). FADD has an amino-terminal death effector domain (DED), which in turn recognizes the DED of procaspase 8 (Muzio et al. 1996). Oligomerization of Fas by Fas-L appears to juxtapose chains of procaspase 8 which consequently undergo auto-cleavage, leading to the release of active caspase 8, initiating a cascade of proteolytic events that result in apoptosis (Salvesen et al. 1999). Thus, rather like a RTK that engages a modular protein (Grb2), which in turn recruits a signaling enzyme (Sos1) to activate the Ras pathway, so Fas binds a modular adaptor, FADD, that couples to the enzyme caspase 8 and lights the apoptotic fuse. These data indicate that receptors involved in signaling pathways that do not use phosphorylation as a primary mechanism for information transfer, nonetheless make use of modular protein-protein interactions to specifically activate their targets.

Other members of the TNF-R superfamily, such as TNF-R1, utilize a death domain to activate cytoplasmic signaling. TNF-R1 interacts initially with the death domain of a scaffolding protein termed TRADD (Hsu et al. 1995), which in turn recognizes the FADD adaptor, as well as a distinct modular protein termed TRAF2 that activates the Jnk MAPK pathway, and a DD-containing protein kinase RIP that stimulates the NFB pathway (Arch et al. 1998) (Fig. 2). Thus TNF-R1, like some RTKs, employs a docking protein that associates with multiple downstream targets and can thereby extend the range and potency of receptor signaling. However, most members of the TNF-R family, including TNF-R2, appear to signal primarily through TRAF proteins. The TRAFs contain a carboxy-terminal domain (TRAF-C) that binds short peptide motifs on the relevant receptor or on docking proteins such as TRADD, preceeded by a coiled-coil region. The amino termini of the TRAFs have ring and zinc finger sequences that are responsible for interactions with downstream targets (Rothe et al. 1994). Crystal structures of the coiled-coil and TRAF-C regions of TRAF2 indicate that these domains self-associate to form a trimer that is ideally fashioned to bind the activated receptor, which is itself coralled into a trimeric state by its ligand (McWhirter et al. 1999; Park et al. 1999; Ye et al. 1999). Thus, although TRAFs have only a low affinity for the monomeric receptor, they bind in a co-operative fashion to the oligomerized receptor. Surprisingly, an individual TRAF-C domain can bind through the same groove to peptide motifs that are unrelated in their primary sequences. Thus, by analogy with RTKs and SH2 domains, the oligomerization of TNF-Rs creates high affinity binding sites for the TRAF-C domains, which recognize specific motifs within the receptor. TRAFs then act as adaptors to link the activated receptors to cytoplasmic targets.

	Specificity in signaling by serine/threonine kinases

Top Introduction Specificity and complexity at... Specific activation of... Multiple modules in signal... Generality of protein-protein... Specificity in signaling by... Scaffolding and docking... Guidance receptors and... Integration of signaling... Evolution of signaling pathways Regulating the intensity of... Conclusions References

RTKs and other cell surface receptors, frequently activate protein serine/threonine kinases that convey the signal to targets in the cytoplasm and nucleus. Clearly, this is an intrinsic function of the TGF receptors, but other receptors must take a more circuitous route to stimulate protein serine/threonine kinase activity. The Ras GTPase, activated by RTKs, binds the c-Raf protein kinase (a MAPK kinase kinase or MAPKKK), which consequently phosphorylates Mek (a MAPKK). Mek is a dual-specificity kinase that phosphorylates and activates Erk (a MAPK), which has multiple substrates involved in the regulation of cell growth and proliferation (Marshall 1994; Whitmarsh and Davis 2000). Similar cascades of protein kinases lead to the activation of other MAPKs, such as Jnk/Sap or p38.

RTKs can also stimulate protein serine/threonine kinases through pathways involving phospholipid production, including the activation of PI3K, which leads to the production of PI-3,4,5-P3. PIP3 binds selectively to the PH domains of the serine/threonine kinases PDK1 and Akt/PKB (Alessi et al. 1997; Belham et al. 1999) inducing their membrane association (Andjelkovic et al. 1999). Interestingly, PDK1 phosphorylates PKB within the activation loop of the catalytic domain, in a fashion that is indispensable for PKB activation and its subsequent effects on events such as cell survival. Furthermore, PDK1 appears to be a more general activator of a family of serine/threonine kinases, including p70S6 kinase, p90Rsk1, and atypical protein kinase C (PKC) isoforms, amongst others. PLC- also regulates signaling to PKCs by stimulating the hydrolysis of PI-4,5-P₂ to yield diacyglycerol and IP₃, which contribute to the activation of conventional PKCs.

Through a series of protein-protein interactions, described in part above, TNF-R1 activates a heteromeric complex comprised of two protein kinase subunits, IKK and IKK and at least one additional component, IKK/Nemo (Rothwarf et al. 1998; Karin 1999). IKK activation leads to the phosphorylation of IB, an inhibitor of the NFB transcription factor, resulting in IB proteolytic destruction. This frees NFB to enter the nucleus and induce the expression of specific genes.

The theme that numerous cell surface receptors activate pathways involving a series of protein serine/threonine kinases raises the issue of how specificity is maintained in such kinase cascades, and how the ultimate phosphorylation of target proteins on serine/threonine modifies their functional properties. The pursuit of the latter question has uncovered a number of modular proteins that physically recognize specific phosphorylated serine/threonine-containing motifs, in a similar fashion to the binding of SH2 or PTB domains to pTyr-containing proteins. 14-3-3 proteins provide the prototype for this idea. Mammalian cells contain seven 14-3-3 isoforms, which form homo- or heterodimers that recognize specific pSer-containing motifs, originally identified as having the consensus Arg-Ser-X-pSer-X-Pro (Muslin et al. 1996). More recent data have revealed the structural basis for this interaction (Yaffe et al. 1997). Of particular interest, some of the proteins involved in the signaling pathways mentioned above are bound by 14-3-3 proteins following their phosphorylation. The protein kinase PKB, for example, phosphorylates the pro-apoptotic proteins BAD and FKHRL1, the former being a Bcl family member that in its unphosphorylated state binds and inhibits the death antagonist Bcl-X_L (Zha et al. 1996), while FKHRL1 is a transcription factor that may induce the expression of pro-apoptotic genes (Brunet et al. 1999). The binding of 14-3-3 proteins to phosphorylated targets apparently results in their relocalization and inhibition. In the case of BAD this is achieved by sequestering it away from Bcl-X_L, while FKHRL1 is apparently retained in the cytoplasm once complexed to 14-3-3, and is therefore prevented from gaining access to its targets in the nucleus. 14-3-3 proteins also interact with the c-Raf kinase to regulate its activity (Thorson et al. 1998), and indeed a dominant negative 14-3-3 protein blocks serum-induced Erk MAPK activation and enhances apoptosis both in cultured cells and in mice (Xing et al. 2000).

The ability of 14-3-3 proteins to control cellular events through the recognition of specific phosphoproteins is not restricted to conventional signaling pathways responsive to extrinsic cues, but is also important in regulating checkpoints in the cell cycle that monitor intrinsic events such as DNA damage. In this context, a key step in controlling the passage of mammalian cells through the cell cycle is the serine phosphorylation of Cdc25C, a tyrosine phosphatase that dephosphorylates and activates the critical cyclin-regulated protein kinase Cdc2, and thereby promotes passage of the cell into mitosis. During interphase Cdc25C is phosphorylated at Ser-216, resulting in binding to 14-3-3 proteins (Peng et al. 1997). Cdc25C shuttles between the cytoplasm and nucleus, and 14-3-3 binding favors the retention of Cdc25C in the cytoplasm, possibly by masking a nuclear localization signal (Fig. 4). As a result Cdc25C is physically separated from its nuclear substrate, which is therefore held in an inactive state. Dephosphorylation of Ser-216 frees Cdc25C to enter the nucleus and initiate mitosis. In yeast, protein kinases that regulate cell cycle checkpoints by responding to DNA damage and replication blocks, such as Cds1 and Chk1, directly phosphorylate Cdc25 and induce a Cdc25/14-3-3 complex, thereby slowing passage through the cell cycle and allowing time for DNA repair (Zeng et al. 1998; Zeng and Piwnica-Worms 1999).

View larger version (32K): [in this window] [in a new window]   Figure 4.   A simplified scheme indicating the role of serine/threonine phosphorylation events in regulating DNA damage-induced cell cycle checkpoint control. DNA damage results in phosphorylation mediated stabilization of p53 by a variety of kinases (ATM, ATR, DNA-PK, Jnk, and CKI). This blocks the interaction of p53 with Mdm2 that normally results in efficient ubiquitin-targeted degradation of p53 by the proteasome. Activated p53 induces the transcription of genes such as p21Cip/Waf, a cyclin dependent kinase inhibitor that blocks the action of CyclinE/Cdk2 and thereby prevents the phosphorylation of targets such as Rb, an event that is required for G1-to-S transition. DNA damage stabilization of p53 thereby blocks cell cycle progression at the G1-to-S checkpoint. Cyclin E1 is itself degraded at the G1-to-S boundary following phosphorylation on Thr-380. Phosphorylation at this site is sufficient to target Cyclin E1 to the SCF E3 ubiquitin ligase complex composed of Cdc53/CUL-1, Skp1, Rbx-1, Cdc34 (E2), and a putative F-box protein. DNA damage also results in the activation of Chk1 kinase that phosphorylates the Cdc25C phosphatase on Ser-216. 14-3-3 protein binds to phosphorylated Cdc25C and sequesters this complex in the cytoplasm. Active Cdc25C is required to activate CyclinB/Cdk2 to allow G2-to-M transition. Thus, DNA damage also blocks cell cycle progression at the G2-to-M checkpoint.

14-3-3 proteins are small, individual polypeptides, and have not as yet been found to be covalently linked to other functional domains. However, there are protein modules with the potential to bind pSer/pThr-containing motifs that, like SH2 domains, are located within a number of different host proteins. Notably, the Forkhead-associated (FHA) domain is present in a wide range of nuclear polypeptides involved in transcription, DNA repair or cell cycle progression in both eukaryotes and prokaryotes (Hofmann and Butcher 1995). Recent work on the yeast protein kinase Rad53 has shown that its amino-terminal FHA domain binds selectively to pThr-X-X-Asp motifs and has suggested that the recognition of phosphorylated peptide motifs may be a common property of FHA domains (Durocher et al. 1999). The structure of the carboxy-terminal PHA domain of Rad53 has recently been solved, revealing a -sandwich with two anti-parallel -sheets (Liao et al. 1999), but the precise mechanism of ligand binding is unknown. Interestingly, Rad53 lies downstream of its phosphorylated binding partner, Rad9, a protein that senses DNA damage, suggesting that a phosphodependent FHA-mediated interaction is important in checkpoint signaling (Sun et al. 1998). Consistent with this idea, recent data indicate that the amino-terminal FHA domain of human Chk2, a homolog of yeast Rad53, is affected by mutations in the familial cancer Li-Fraumeni syndrome (Bell et al. 1999).

There are increasing examples of pSer/pThr-dependent protein-protein interactions. Phosphorylation of the transcription factor CREB at Ser-133 by protein kinases such as cAMP-dependent protein kinase (PKA), PKB, and p90Rsk2 creates a binding site for the coactivator CBP, and results in transcriptional activation of CREB-responsive genes (Xing et al. 1996; Radhakrishnan et al. 1997; Du and Montminy 1998). Similarly, the WW domain of the peptidyl-prolyl isomerase Pin1 binds pSer-Pro motifs, which may position the enzyme close to its substrates (Lu et al. 1999).

Equally striking, the pSer/Thr-dependent recognition of proteins by members of the F-box family appears to be a common and critical mechanism for the selective destruction of signaling and cell cycle proteins by ubiquitin-mediated proteolysis (Craig and Tyers 1999; Tyers and Willems 1999). This scheme was first established for a complex of proteins (termed SCF) that control S phase progression in Saccharomyces cerevisiae, through their ability to degrade their targets in a fashion that imposes order on the cell cycle (Willems et al. 1996; Skowyra et al. 1997; Patton et al. 1998). In yeast, a protein termed Cdc53 (corresponding to the cullins of multicellular organisms) serves as a scaffold to recruit an adaptor (Skp1), an E2 protein-ubiquitin ligase (Cdc34), and a ring finger protein (Rbx1), which potentiates substrate ubiquitination. Skp1 links the Cdc53 complex to one of many proteins with a conserved Skp1-binding domain, termed an F box. F-box proteins contain the eponymous F box at the amino terminus and a variable carboxyl terminus, typically comprised of WD40 repeats or leucine-rich repeats, which directly contacts the target for ubiquitination. In several cases, phosphorylation of the target is required for its association with the F-box protein. This has been nicely demonstrated for the yeast protein Sic1, which is the only essential target for Cdk activity during the G₁ phase of the cell cycle. Sic1 is an inhibitor of the G₂/M phase Cdk complex, and its inactivation by proteolytic degradation, is required for passage through the cell cycle. Sic1 becomes phosphorylated at multiple serine residues and subsequently associates with the carboxy-terminal WD40 repeats of an F-box protein termed Cdc4, resulting in its degradation. The targeting of specific proteins for degradation through their association with F-box proteins likely regulates many events in signal transduction (Fig. 4). As an example, phosphorylated IB is recognized by TrCP, a mammalian F-box protein with carboxy-terminal WD40 repeats, that is closely related to the yeast Cdc4 (Yaron et al. 1998; Winston et al. 1999). Thus a pivotal event in TNF-R signaling involves the phospho-dependent recognition of the IB inhibitor by an F-box protein.

	Scaffolding and docking interactions in protein serine/threonine kinase pathways

Top Introduction Specificity and complexity at... Specific activation of... Multiple modules in signal... Generality of protein-protein... Specificity in signaling by... Scaffolding and docking... Guidance receptors and... Integration of signaling... Evolution of signaling pathways Regulating the intensity of... Conclusions References

The data summarized above have indicated that the phosphorylation of serine/threonine residues directly regulates protein-protein interactions. Many of the signaling pathways that control serine/threonine phosphorylation are composed of a succession of protein kinases (MAPK cascades for example), raising the issue as to how specificity is preserved under such circumstances. Clearly, protein serine/threonine kinases preferentially phosphorylate specific motifs in their substrates, but the experience with tyrosine kinases suggests that they might have more extensive interactions with their targets. Indeed, two types of docking interactions appear important in determining specificity in pSer/Thr signaling. Protein kinases are often anchored to a scaffolding protein that may either facilitate the flow of information from one kinase to another, or hold the kinase in a latent state close to the receptor that will induce its activation (Pawson and Scott 1997; Whitmarsh and Davis 1998). Furthermore, MAPKs appear to have specific docking interactions with their immediate substrates and regulators that likely enhance the specificity of MAPK pathways (Holland and Cooper 1999) (Fig. 5).

View larger version (45K): [in this window] [in a new window]   Figure 5.   Scaffold mediated assembly of signaling pathways. (A) Jip1 acts as a scaffold for the mammalian Jnk MAPK cascade. Jip1 has separate binding sites for Jnk, and the upstream kinases MKK7 (MAPKK), MLK3 (MAPK), and HPK1. Jip1 also has SH3 and PTB domains that may tether the complex to additional proteins involved in upstream activation or localization. (B) The Erk MAPK docks to target proteins. Once tethered in this manner, Erk phosphorylates the substrate, Rsk1. (C) The regulatory cyclin A subunit of Cdk2 binds substrates with a conserved RXL motif, such as p107. (D) The AKAP protein Yotiao binds to the NMDA receptor, PKA in the inactive form, and PP1 in the active form. In doing so, Yotiao creates close physical association of the components that repress resting NMDA receptor and enhance channel activation.

The classical example of this latter type of scaffolding protein is the Ste5 polypeptide in yeast, which is required for growth arrest and mating, and acts downstream of the G-protein coupled pheromone receptor to regulate a MAPK cascade (Elion 1998). Ste5 interacts with the G subunit (Ste4) (Pryciak and Huntress 1998), and has independent binding sites for a MAPKKK (Ste11), a MAPKK (Ste7), and a MAPK (Fus3) (Choi et al. 1994). Various functions have been proposed for Ste5, notably to increase the fidelity of the pathway by physically juxtaposing successive kinases, to localize these kinases to specific subcellular compartments, and to insulate interacting kinases from separate pathways. It is also possible that Ste5 oligomerization could enhance kinase activation by promoting intermolecular autophosphorylation. The potential importance of scaffolding proteins is underscored by the observation that the MAPKKK Ste11 also acts in the yeast osmosensing pathway, although the other components of the pathway, including the Hog1 MAPK are different. In this case, the MAPKK Pbs2 provides the scaffolding function through an extended amino terminus. Pbs2 engages both Ste11 and Hog1, as well as the osmosensing receptor (Sho1), which has an SH3 domain that binds a proline-rich motif in Pbs2 (Posas and Saito 1997). Thus, Pbs2 serves a somewhat analagous function to Ste5 in assembling the elements of a signaling pathway into an individual complex.

Recent data suggest that scaffolding proteins akin to Ste5, likely play an important role in organizing MAPKs in mammalian cells. In particular, several proteins have been identified that bind members of the Jnk MAPK pathway and potentiate Jnk activation (Yasuda et al. 1999; Kelkar et al. 2000). JIP1 and JIP2 are closely related proteins that have separate binding sites for Jnk, and the upstream kinases MKK7 (a MAPKK), MLK3 (a MAPKKK), and HPK1, a Ste20-related kinase that activates MLK3 (Fig. 5A). JIP1/2 appear to be activators of Jnk signaling, and can form large cytoplasmic complexes through their ability to make homo- or hetero-oligomers. They are relatively selective for specific members of the Jnk signaling cassette, suggesting that they serve both to enhance activation and to impose specificity. Interestingly, these JIP proteins have carboxy-terminal SH3 and PTB domains, which might aid in their localization, or association with other signaling proteins. Indeed the JIP-1 PTB domain binds a RhoGEF, and JIP-1 is localized to the tips of neurites in cultured neuronal cells (Meyer et al. 1999).

In addition to the indirect association of MAPKs and their upstream regulators, mediated by their common interaction with the same scaffolding protein, MAPKs can bind directly to their substrates and regulators through noncatalytic docking sites. Like other protein kinases, the Erk and Jnk MAPKs preferentially phosphorylate serine or threonine in a specific consensus sequence, minimally Ser/Thr-Pro. However, this does not fully explain the specificity of MAPK substrate selection in vivo. Rather, it appears that physiological substrates for MAPKs have separate motifs that tether the enzyme to its phosphorylation target. A common docking site for the Erk MAPK is formed by a short stretch of basic residues, found in substrates such as the protein kinases Rsk1/2 and Mnk2, and markedly increases the efficiency with which they are phosphorylated (Waskiewicz et al. 1997; Gavin and Nebreda 1999). The docking motif binds a negatively charged region carboxy-terminal to the Erk catalytic domain. Remarkably, the same basic motif is found in a kinase (Mek) and phosphatase (MKP) that respectively phosphorylate and dephosphorylate Erk, suggesting that substrates and regulators may compete for the same binding site on the Erk protein kinase (Tanoue et al. 2000). A similar common docking (CD) domain is found in the Jnk and p38 MAPK family members, and also appears to specify interactions with substrates and regulators. A distinct docking site (FXFP) is found in Erk substrates such as the Elk-1 transcription factor, and its presence markedly enhances the affinity with which the kinase and substrate interact, resulting in enhanced phosphorylation (Jacobs et al. 1999). Elk-1 has an additional docking motif, the D box, that binds both to Erk and Jnk, and is related to the  domain in c-Jun that confers high affinity binding to Jnk. Interestingly, these motifs are portable, in the sense that they will convert a poor target into a high affinity substrate for the relevant MAPK, and act in synergy to enhance phosphorylation.

Results of this type have suggested that MAPKs, and possibly many other serine/threonine kinases, select their substrates first through a noncatalytic docking interaction, which determines the substrate to be phosphorylated. This is followed by the recognition of a specific site within the bound protein for phosphorylation at the enzyme's active site (Fig. 5B). Indeed the regulatory cyclin A subunit of Cdk2 binds substrates with a conserved RXL motif, such as p107, in a fashion that is important for their subsequent phosphorylation (Schulman et al. 1998) (Fig. 5C). In a related vein, specific cyclins in yeast (Pcl8/Pcl10) direct the Pho85 Cdk to phosphorylate glycogen synthase and thereby antagonize glycogen accumulation (Huang et al. 1998). In principle, these mechanisms through which protein serine/threonine kinases increase the local concentration of their physiological substrates is very similar to the devices by which tyrosine kinases attract their targets. Thus, it appears that docking interactions of this sort may be a very general phenomenon in the recognition of protein kinase substrates and therefore in determining the specificity of signal transduction.

The ability of scaffolding proteins to organize the protein kinases and phosphatases that regulate serine/threonine phosphorylation is typified by the A kinase anchoring proteins (AKAPs) (Colledge and Scott 1999). These represent a growing family of large polypeptides, that contain binding sites for various protein serine/threonine kinases and phosphatases, as well as a targeting motif that directs the resulting complex to a specific site in the cell. PKA has a catalytic subunit (C) whose activity is repressed by binding to a regulatory (R) subunit. Receptors such as GPCRs elevate the level of cAMP, which binds to the R subunit and induces dissociation of a free C subunit. In addition to its cAMP-binding sites, the R subunits have an amino-terminal domain required for dimerization and binding to the AKAP. In the case of the RII subunit, the dimerized amino terminus forms a four-helix bundle that creates a groove to accommodate an amphipathic -helix from the AKAP (Newlon et al. 1999). Thus a short motif on the AKAP binds the RII subunit of PKA, holding the kinase in an inactive state at a subcellular site dictated by the AKAP. AKAPs bind not only to PKA, but also to other protein kinases such as PKC isoforms, as well as serine/threonine phosphatases (PPI and PPII). In general, the AKAPs appear to anchor the kinases and phosphatases in an inactive state, close to their activators and substrates. Yotiao is a ~210-kD protein that interacts directly with the NR1A subunit of the NMDA receptor and binds both the RII subunit of PKA in an inactive state, as well as the phosphatase PP1 in an active form (Westphal et al. 1999). NMDA receptor channel activity is positively regulated by phosphorylation, and by physically linking a constitutively active phosphatase to NR1A, Yotiao appears to repress the activity of the channel under resting conditions. However, the simultaneous juxtaposition of inactive PKA with the receptor means that Yatiao also enhances channel activation once cAMP liberates an active C subunit, overcoming the inhibitory activity of the phosphatase (Fig. 5D). Thus protein-protein interactions appear to be an important determinant of specificity in signaling by neurotransmitter receptors. This theme that has been echoed by the discovery of a complex network of interacting proteins in the post-synaptic density, that largely through PDZ domain-mediated interactions appears to organize the localization and signaling activities of glutamate receptors and GPCRs (Fanning and Anderson 1999; Tu et al. 1999).

	Guidance receptors and signaling to the cytoskeleton

Top Introduction Specificity and complexity at... Specific activation of... Multiple modules in signal... Generality of protein-protein... Specificity in signaling by... Scaffolding and docking... Guidance receptors and... Integration of signaling... Evolution of signaling pathways Regulating the intensity of... Conclusions References

It is common when considering signaling pathways to dwell on events that culminate in the nucleus. However, signaling pathways that control the cytoskeleton and adhesion of cells to the extracellular matrix are essential for guided cell migration, including processes such as axon guidance and topographic map formation in the brain. Recent work has identified a number of cell surface receptors that mediate the responses of axons to both repulsive and attractive cues, and which play a larger role in the guided movement of multiple cell types (Tessier-Lavigne and Goodman 1996). Among these guidance receptors are members of the Eph family of RTKs. Mammalian Eph receptors interact with ligands, termed ephrins, which are themselves anchored to the cell surface, either through a GPI linkage (A-type ephrins) or a transmembrane sequence joined to a conserved cytoplasmic tail (B-type ephrins) (Holder and Klein 1999). Physiological Eph receptor activation apparently requires a direct interaction between receptor and ephrin-expressing cells. Upon activation, Eph receptors undergo autophosphorylation at multiple sites, including the kinase domain activation loop and at tyrosine residues within a conserved motif in the juxtamembrane region (Kalo and Pasquale 1999). Surprisingly, the juxtamembrane autophosphorylation sites appear to have a dual function since they contribute to receptor kinase activation, as well as providing docking sites for proteins with SH2 domains (Holland et al. 1997; Binns et al. 2000; Zisch et al. 2000). In addition to binding SH2 proteins directly, Eph receptors can phosphorylate docking proteins such as p62^dok, which engages Ras GAP and the SH2/SH3 adaptor Nck through SH2-mediate interactions (Holland et al. 1997).

Eph receptors have many functions in vertebrates and invertebrates, including regulation of angiogenesis, the formation of boundaries between rhombomeres, formation of the palate, and tissue morphogenesis. However, they have been most intensively studied for their role in axon guidance and topographic map formation in the central nervous system (Flanagan and Vanderhaeghen 1998). The binding of ephrins to neuronal cells expressing Eph receptors induces remodeling of the actin cytoskeleton and growth cone collapse, in a fashion that is dependent on receptor kinase activity and the juxtamembrane pTyr sites (Drescher et al. 1995; Binns et al. 2000). These data suggest that activated Eph receptors can communicate with signaling proteins that regulate the cytoskeleton. There are a number of candidates that might fulfil this role, including the Nck adaptor.

Nck has a carboxy-terminal SH2 domain that binds pTyr sites, and three amino-terminal SH3 domains that engage a variety of proteins implicated in cytoskeletal organization (Buday 1999). In particular, the second SH3 domain of Nck binds the protein serine/threonine kinase Pak (Bokoch et al. 1996; Lu et al. 1997) (Fig. 6). Pak has a carboxy-terminal kinase domain, and an extended amino terminus that binds the SH3 domains of both Nck and a Rac/Cdc42 GEF termed PIX (Manser et al. 1998), as well as recognizing GTP-bound Rac/Cdc42 GTPases. Nck recruits Pak to the membrane, whereas binding of Cdc42 appears to directly increase Pak kinase activity, likely by causing a conformational change that releases an inhibitory effect of the amino terminus. Thus, Pak may have two ways to modify the actin cytoskeleton. One being a kinase-dependent effect through phosphorylation of substrates such as myosin light-chain kinase (Sanders et al. 1999), whereas the interaction with PIX can deliver a kinase-independent signal through Cdc42/Rac activation (Fig. 6).

View larger version (22K): [in this window] [in a new window]   Figure 6.   A signaling pathway to the cytoskeleton. Axon guidance receptors potentially bind the Nck adaptor, through both SH2-and SH3-mediated interactions. The second SH3 domain of Nck recruits the Pak protein serine/threonine kinase to the membrane. Pak kinase activity is induced by binding of GTP-Cdc42 to a CRIB motif. Pak can also generate activated Cdc42 through the associated PIX GEF. (Pro, proline-rich motif).

Genetic data from Drosophila support the idea that Nck and Pak are important for the control of axon guidance. Mutations in the Drosophila Nck homolog (termed Dreadl