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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Nat Struct Mol Biol. Author manuscript; available in PMC Jul 27, 2009.
Published in final edited form as:
PMCID: PMC2716141

Release of autoinhibition of ASEF by APC leads to CDC42 activation and tumor suppression


Autoinhibition of the Rho guanine nucleotide exchange factor ASEF is relieved by interaction with the APC tumor suppressor. Here we show that binding of the armadillo repeats of APC to a ‘core APC-binding’ (CAB) motif within ASEF, or truncation of the SH3 domain of ASEF, relieves autoinhibition, allowing the specific activation of CDC42. Structural determination of autoinhibited ASEF reveals that the SH3 domain forms an extensive interface with the catalytic DH and PH domains to obstruct binding and activation of CDC42, and the CAB motif is positioned adjacent to the SH3 domain to facilitate activation by APC. In colorectal cancer cell lines, full-length, but not truncated, APC activates CDC42 in an ASEF-dependent manner to suppress anchorage-independent growth. We therefore propose a model in which ASEF acts as a tumor suppressor when activated by APC and inactivation of ASEF by mutation or APC truncation promotes tumorigenesis.

The adenomatous polyposis coli (APC) protein is a negative regulator of the Wnt signaling pathway and promotes the phosphorylation and degradation of β-catenin1. The majority of colorectal cancers (CRCs) harbor C-terminally truncated forms of APC that retain the N-terminal coiled-coil domain and the highly conserved armadillo repeat region (APCArm)2 and are unable to regulate the degradation of β-catenin3. Recent studies suggest that APC regulates cytoskeletal dynamics to influence cellular migration, cell division, polarization and adhesion, and it seems increasingly likely that deregulated cytoskeletal dynamics, together with enhancement of transcription by β-catenin, potentiate tumor formation and progression upon APC truncation.

APC may regulate cytoskeletal networks by binding to microtubules and to proteins implicated in reorganization of the actin cytoskeleton, such as the Rho effectors mDia and IQGAP1 and the Rho guanine nucleotide exchange factor (RhoGEF) ‘APC-stimulated guanine nucleotide exchange factor’ (ASEF, also called ARHGEF4)4. ASEF is a Dbl-family GEF that contains an Src-homology-3 (SH3) domain followed by the Dbl-homology (DH) and pleckstrin-homology (PH) domains characteristic of Dbl-family GEFs that specifically activate members of the Rho family of GTPases. DH and PH domains in Dbl proteins catalyze the exchange of GDP for GTP in Rho GTPases, allowing them to signal to downstream effectors5. ASEF is homologous to the Dbl proteins collybistin (also called PEM2) and SPATA13 (also called ASEF2), both of which have been shown to activate specifically CDC42 and not other Rho-family GTPases6,7.

Previous data suggest that ASEF exists in an autoinhibited form and is activated upon binding of APCArm to the region termed the APC-binding region (ABR)8. Binding of APCArm to the ABR stimulates activation of the Rho GTPase RAC1 by ASEF. Furthermore, truncation of the ABR is sufficient to relieve autoinhibition, rendering ASEF constitutively active. In addition, truncated, but not wild-type, APC has been shown to efficiently activate ASEF to promote cancer cell migration9.

In this study, we wished to delineate the molecular mechanism by which APC relieves autoinhibition of ASEF to stimulate its GEF activity and to assess the contribution of ASEF to CRC tumorigenesis. To our surprise, and in contrast to previous reports, we found that ASEF specifically activated CDC42, but not RAC1 or other Rho GTPases, in vitro and in vivo. Furthermore, whereas binding of APCArm to ASEF stimulated robust exchange activity on CDC42, truncation of the ABR of ASEF did not activate ASEF. Instead, truncation of the SH3 domain was required to activate the exchange activity of ASEF toward CDC42. Indeed, a 2.25-Å -resolution structure of an autoinhibited form of ASEF revealed that the SH3 domain of ASEF forms a tight and extensive interface with both the DH and PH domains to effectively block access of CDC42 to the GTPase-binding site. Also in contrast to previous data9, we show that ASEF functions downstream of full-length APC, but not its truncated form, to activate CDC42. Silencing the expression of ASEF in CRC cell lines expressing wild-type, but not truncated, APC resulted in a considerable growth advantage for these cells. Finally, we show that a recently identified mutation in ASEF found in breast cancer abolishes the GEF activity of ASEF. These data suggest that ASEF is a tumor suppressor that links full-length APC to CDC42 and that its inactivation, by mutation of either APC or ASEF, promotes cancer progression.


ASEF is a RhoGEF specific for CDC42

Previous structural analyses of RhoGEFs bound to their cognate Rho GTPases provide guidelines for predicting the GTPase specificities of DH domains on the basis of their primary sequences1014. DH domains of RAC1-specific GEFs such as Tiam1 and TRIO typically have isoleucine (Ile1187 in Tiam1) in a position where DH domains of CDC42-specific GEFs, such as Intersectin (ITSN) and PEM2/collybistin, have leucine (Leu1376 in ITSN) (Fig. 1a). ASEF features a leucine (Leu421) at the position equivalent to Ile1187 of Tiam1, suggesting that ASEF might be specific for CDC42. Indeed, a fragment of ASEF encompassing the DH and PH domains catalyzed nucleotide exchange specifically on CDC42 but not RAC1 or RHOA (Fig. 1b). Furthermore, ASEF showed no exchange activity toward other Rho family members, including RHOB, RHOC, RAC2, RAC3, RHOG, TC10, TCL and RHOF (Supplementary Fig. 1 online and data not shown). Moreover, an L421I substitution in the DH/PH fragment of ASEF conferred the capacity to activate RAC1 at the expense of CDC42 (Fig. 1c). These data confirm the importance of Leu421 of ASEF in dictating specificity toward CDC42 while prohibiting RAC1 activation.

Figure 1
ASEF is a GEF specific for CDC42

We assessed the in vivo specificity of ASEF for Rho GTPases by monitoring effects of ASEF expression on the actin cytoskeleton, which undergoes distinct morphological rearrangements in response to the activation of different Rho GTPases15. Overexpression of a DH/PH fragment of ASEF fused to yellow fluorescent protein (YFP–ASEF DH/PH) in NIH3T3 mouse fibroblasts resulted in spindle-like projections rich in F-actin, similar to the filopodia induced by activated CDC42 fused to green fluorescent protein (GFP–CDC42 61L) but not the lamella induced by activated RAC1 fused to GFP (GFP–RAC1 61L) (Fig. 2a). The isolated CRIB domain from the CDC42-specific effector N-WASP (N-WASP CRIB) binds to, and blocks signaling downstream of, active CDC42 but not RAC1 in a dominant-negative fashion16. Coexpression of N-WASP CRIB with either GFP–CDC42 61L or YFP–ASEF DH/PH effectively suppressed the formation of filopodia. In contrast, N-WASP CRIB did not block lamella formation induced by RAC1 (Fig. 2b). Therefore, in contrast to its original characterization, ASEF specifically activates CDC42 and not other Rho GTPases in vitro and in vivo.

Figure 2
ASEF induces filopodia in NIH3T3 fibroblasts

ASEF is autoinhibited by the SH3 domain

The primary ASEF isoform expressed in human tissues is encoded by ARHGEF4 (ref. 17; here called ASEF). This isoform contains sequences on the N-terminal side of the ABR domain that are distinct from those encoded in the gene that was originally cloned8.We therefore used this predominant isoform throughout the experiments below as full-length ASEF (residues 1–690; see Supplementary Methods.online).

To map regions within ASEF necessary for the autoinhibition of exchange activity, a series of truncated forms of ASEF (Fig. 3a) were tested for their capacity to activate CDC42 in vitro. To our surprise, and in contrast to previous reports8,9, truncation of the N terminus alone (ΔN) or together with part or all of the ABR (ΔABR1–ΔABR4) did not elicit guanine nucleotide exchange on CDC42 (Fig. 3b). However, further N-terminal truncation to remove the SH3 domain of ASEF (DH/PH) greatly increased the exchange activity of ASEF toward CDC42. We found similar results upon overexpression of N-terminally truncated forms of ASEF in NIH3T3 cells (Fig. 3c). That is, full-length ASEF, as well as N-terminally truncated ASEF lacking its ABR but retaining its SH3 domain (ΔABR4), were incapable of producing CDC42-like filopodia. In contrast, ASEF DH/PH, which lacks both the ABR and SH3 domains, induced filopodia formation (Fig. 2a and Fig. 3c). Therefore, the SH3 domain is fully responsible for autoinhibition of the exchange activity of ASEF in vitro and in vivo, and regions on the N-terminal side of the SH3 domain, including the ABR, are irrelevant for this autoinhibition. Attempts to measure increased CDC42-GTP in cells expressing ASEF by affinity precipitation assays were unsuccessful owing to persistent elevated CDC42-GTP levels in the absence of serum (data not shown, and refs. 18,19).

Figure 3
ASEF is autoinhibited by the SH3 domain

Identification of the core APC-binding motif

The ABR is a 53-residue region of ASEF necessary for interaction with the armadillo repeats of APC. The ABR is conserved among ASEF orthologs and is approximately 50% identical in sequence to the ABR of ASEF2. Collybistin does not contain an ABR region6,20 and therefore is not regulated by APC (data not shown).

To identify specific functional determinants within the ABR, N-terminally truncated forms of ASEF were tested for their capacity to activate CDC42 in the presence of the full armadillo repeat array of APC. As expected, incubation of ASEF ΔN with APCArm stimulated the guanine nucleotide exchange activity of ASEF toward CDC42, whereas ASEF ΔABR4, which completely lacks the ABR, was not stimulated by APCArm (Fig. 4a). Furthermore, ASEF ΔABR1, ASEF ΔABR2 and ASEF ΔABR3 were activated by APCArm similarly to ASEF ΔN. These results indicate that the minimal ABR sequence (residues 183–193) encompassed in ASEF ΔABR3 and lacking in ASEF ΔABR4 is absolutely required for interaction with APCArm and concomitant activation of CDC42 by ASEF. This region, which we term the core ATP-binding (CAB) motif, is immediately adjacent to the SH3 domain on the N-terminal side and is strictly conserved in ASEF2 (Fig. 4b).

Figure 4
Identification of CAP motif in ASEF and ASEF2

The ASEF-related homolog ASEF2 shows high sequence conservation with ASEF, and, like ASEF, its GEF activity is stimulated by APCArm. However, APCArm has been reported to interact with the SH3 domain and not the ABR of ASEF2 to stimulate GEF activity7. We found that ASEF2 ΔN (containing the ABR) was robustly stimulated by APCArm to catalyze nucleotide exchange on CDC42, whereas ASEF2 ΔABR4 (no ABR) was not (Fig. 4c). Therefore, as with ASEF, the ABR region within ASEF2 is essential for activation of RhoGEF catalytic function by APCArm. Given the strict conservation of the CAB motif in both ASEF and ASEF2, it is highly likely that the CAB motif of ASEF2 is absolutely required for binding to APC.

Full-length but not truncated APC activates ASEF

APC mutants associated with CRCs lack binding sites for microtubules and β-catenin but retain the oligomerization domain and the highly conserved ARM repeats (residues 335–735)21 (Fig. 5a). To directly assess the capacity of APC to activate ASEF, we expressed these proteins in COS-7 cells, where the subcellular localization of exogenous full-length or truncated forms of APC recapitulates their endogenous localization in CRC cell lines22,23. Of note, in COS-7 cells, overexpression of activated CDC42 (GFP–CDC42 61L) results in the formation of dorsal and peripheral membrane ruffles, whereas activated RAC1 in COS-7 cells induces peripheral ruffles that are thicker and morphologically distinct24 (Fig. 5b). Consistent with our previous data, activated ASEF (YFP–ASEF DH/PH) induces membrane ruffles in COS-7 cells indistinguishable from those induced by constitutively active CDC42.

Figure 5
Differential activation of ASEF by full-length and truncated APC

When expressed separately, both GFP-tagged APCArm and mCherry-tagged full-length (FL) ASEF showed diffuse nuclear and cytoplasmic localization (Fig. 5c) with no obvious changes in cell morphology compared to cells expressing mCherry alone. However, coexpression of GFP-APCArm and mCherry–FL ASEF resulted in their colocalization in prominent peripheral (arrow) and dorsal (arrow-head) ruffles. Colocalization and ruffle formation were abrogated if the expressed APCArm protein harbored a point mutation (N507K; Fig. 5c) previously shown to prevent interaction of APC with ASEF (Supplementary Fig. 2 online and ref. 25). Furthermore, consistent with our in vitro data, concomitant colocalization and ruffle formation were lost when APCArm was coexpressed with a version of ASEF lacking the ABR (mCherry–ASEF ΔABR4).

Nonsense mutation of codon 1061 results in a common germline truncation of APC associated with CRCs2 (Fig. 5a). In agreement with published reports22,26, exogenously expressed GFP-tagged full-length APC localized to a filamentous meshwork likely to be the microtubule cytoskeleton, whereas a similar construct of APC terminating at position 1061 (APC 1061) was distributed diffusely and in intermittent dense puncta throughout the cytoplasm (Fig. 5d). Notably, when GFP–FL APC was coexpressed with mCherry–FL ASEF, the two proteins colocalized in dorsal ruffles and in puncta close to the plasma membrane (Fig. 5d, inset), suggesting that they interact to activate CDC42. Furthermore, the N507K mutation in the context of full-length APC (GFP–FL APC N507K) disrupted colocalization with mCherry–FL ASEF, and no dorsal ruffles were observed. Contrary to the previous suggestion that truncated APC activates ASEF in vivo9, GFP–APC 1061 did not colocalize with mCherry–FL ASEF or promote membrane ruffling. Therefore, we conclude that full-length APC, but not a form terminating at residue 1061, readily stimulates ASEF in COS-7 cells.

Structure of autoinhibited ASEF

ASEF ΔABR2 is a minimal fragment of ASEF that is completely inhibited in the absence of APC (Fig. 3b) yet fully activated by APCArm (Fig. 4a). To elucidate the structural basis for the autoinhibition of ASEF and its related activation by APC, we determined a high-resolution structure of ASEF ΔABR2 (residues 170–632) by X-ray crystallography (Supplementary Fig. 3 online).

At the heart of the structure is the SH3 domain, which organizes the inhibited conformation of ASEF (Fig. 6a). The five β-strands of the ASEF SH3 domain form a β-barrel similar to other SH3 domains. Other common features include the RT loop (between β1 and β2) and the n-Src loop (between β2 and β3), which typically engage peptide ligands containing multiple prolines27, as well as a short 310-helix separating β4 and β5. Capping the end of the β-barrel is the CAB motif, which forms an extended region (residues 183–186) and a short α-helix (αCAB, residues 187–193). αCAB within the CAB motif primarily interacts with the SH3 domain through contacts with β2 and the n-Src loop. Residues Glu183, Leu185, Glu189 and Asp193 within the CAB motif are solvent exposed and evolutionarily conserved among ASEF homologs, indicating that they may be important for interaction with APC.

Figure 6
Structure of autoinhibited ASEF

The SH3 domain forms an extensive interface primarily with the DH domain, but major interactions also include the PH domain. Of the 4,170 Å2 of solvent-accessible area on the surface of the ASEF SH3 domain, 1170 Å2 are buried through interaction with the DH and PH domains. Elements from the SH3 domain, including β1, the RT loop, the 310-helix, β5 and the extended region on the C-terminal side of β5, form multiple polar and nonpolar interactions with α1, α5 and α6 of the DH domain. This region of the DH domain is the conserved surface that is responsible for binding to the switch regions of nucleotide-free Rho GTPases, as required for their activation by catalyzed guanine nucleotide exchange10. Therefore, in this form, the SH3 domain would block access of CDC42 to the DH domain of ASEF, providing the structural basis for the autoinhibition of ASEF by its SH3 domain as described above. Important interactions are also observed between the SH3 domain and the PH domain, occurring between the RT loop of the SH3 domain and β1 and β2 of the PH domain and between the β3-β4 loop of the SH3 domain and αC of the PH domain. Helix α6 of the DH domain is extended and similar in length to α6 in ITSN and Tiam1 (refs. 10,14) but adopts a unique arched conformation not observed in other DH domains. The arch allows α6 to conform to the surface of the SH3 domain, and this configuration is stabilized by the extensive interactions between the SH3 domain, α6 and the PH domain. This arrangement suggests that in the absence of the SH3 domain—for example, in truncated variants or upon movement of the domain by engagement of APC—α6 will adopt an alternative conformation.

Although the SH3 domain of ASEF forms a unique interface with DH and PH domains that is distinct from those observed between other SH3 domains and polyproline (PXXP)-containing peptides, the PXXP recognition surface is partially occluded (see Supplementary Fig. 4 online). Therefore, in the observed orientation, the binding of PXXP sequences to the SH3 domain remains energetically unfavorable. An in-depth description of the PXXP-binding site of ASEF is available in the Supplementary Data and Supplementary Discussion online.

Comparison of ASEF with collybistin DH/PH–CDC42

Collybistin is a Dbl-family RhoGEF that specifically activates CDC42 (ref. 6) and is highly similar to ASEF; their respective DH and PH domains are 68% identical. A recent structure encompassing the DH/PH cassette of collybistin bound to nucleotide-depleted CDC42 (ref. 28) highlights considerable repositioning of the α6 helix of its DH domain, relative to the structure of ASEF described here (Fig. 6b). In free ASEF, α6 curves toward the main body of the DH domain and is secured in this conformation by the SH3 domain. Modeling CDC42 from the structure of collybistin–CDC42 onto the GTPase-binding site of ASEF reveals that the DH and PH domains of ASEF would prohibit CDC42 binding and exchange irrespective of the SH3 domain. In this inhibited conformation, α6 would impinge upon switch 2 of CDC42, and regions in the PH domain would clash with α3a, α3b and α4 of CDC42. To relieve this steric clash, the DH and PH domains of ASEF must adopt a more open conformation, probably one similar to that observed in collybistin–CDC42. In doing so, α6 must rotate ~45°, to a position more parallel to the main body of the DH domain, to facilitate an ~30-Å translation of the PH domain. Molecular dynamics simulations of ASEF have also suggested conformational flexibility between the DH and PH domains29. Additionally, in the structure of collybistin–CDC42, the region on the C-terminal side of αC (αC extension) becomes ordered and packs against the C terminus of αC, presumably to stabilize this conformation. Although the ASEF ΔABR2 construct used for crystallization encompasses the equivalent αC extension, electron density in this region is missing from the structure.

From these observations, a mechanism of ASEF activation emerges in which binding of the ABR of ASEF by APC retracts the SH3 domain from the DH and PH domains, allowing the GEF to relax into an open and active conformation. Previously determined structures of DH and PH domains have intimated plasticity of α6, especially in the DH and PH domains of Sos1 (ref. 30). The present comparison of ASEF and collybistin structures reveals large domain rearrangements of DH/PH cassettes required for regulating the autoinhibition and subsequent activation of Dbl-family GEFs.

Interface of the SH3 domain with the DH and PH domains

The DH and PH domains of ASEF form an arch stabilized at its center by the SH3 domain (Fig. 7a). Two sets of hydrophobic interactions in the crown of the arch are crucial for stabilizing the interface. Chief among these are the interactions of Trp203 at the base of the RT loop of the SH3 domain, which act as the keystone by packing into a central hydrophobic pocket formed by residues in α5 and α6 of the DH domain. A hydrogen bond between the indole nitrogen of Trp203 and the sulfhydryl group of Cys428 cements the interactions. Also within the RT loop, Met208 inserts into a second hydrophobic pocket framed by residues from α6 of the DH domain and β1 and β2 of the PH domain, and these interactions seem to be crucial for maintenance of the arched conformation of the DH and PH domains. In between Trp203 and Met208 of the RT loop, Asp204 forms hydrogen bonds with the side chain of Asn466 within α6, and the backbone oxygen of Val206 interacts with the side chain of Lys477 to further stabilize the arch. Asn466 is highly conserved in DH domains, where it is required to bind switch 2 of Rho GTPases during nucleotide exchange5; thus, its central position within the interface with the SH3 domain emphasizes the overlap between binding sites in the DH domain for the SH3 domain and for CDC42.

Figure 7
Detailed view of the SH3 domain interface

Bracketing Trp203 and Met208 are sets of hydrophilic interactions that further stabilize the arched conformation of the DH and PH domains. For instance, Asp210 in the RT loop forms a salt bridge with Lys533 in β3 of the PH domain, and Asp238 in the β3–β4 loop of the SH3 domain binds Arg596 in αC of the PH domain. On the opposite end of the arch and juxtaposed to the ABR, a network of hydrogen bonds centered on Glu436 in α5 of the DH domain stabilizes this portion of the interface. Arg249 in β5 of the SH3 domain is particularly important; its side chain inserts between Glu436 and Glu291 in α1 to form an electrostatic bridge between the three residues. Of note, Glu291 is also crucial to the GEF activity of DH domains, as it is needed to form conserved interactions with switch 1 of Rho GTPases5. In addition to interactions with Arg249, Glu436 also forms hydrogen bonds to the backbone atoms of Val252 and Asn253, on the C-terminal side of β5 of the SH3 domain. The side chain of Asn253 forms important interactions with the side chain of Asn287 in α1 of the DH domain to secure this end of the interface. Because this network of hydrophilic interactions is adjacent to the CAB region within the ABR, we suggest that these interactions are the first to be disrupted upon APC binding and that this disruption is followed by ‘unzipping’ of the remainder of the interface to activate ASEF.

We mutated residues in the SH3 domain that interact with the DH and PH domains of ASEF to alanines, with the anticipation that disrupting this interface might relieve the autoinhibition of ASEF. Individual substitutions were made in the background of fully inhibited ASEF ΔABR2, and mutant proteins were tested for GEF activity in vitro (Fig. 7b). Mutation of residues that form interactions with the main body of the DH domain (Trp203, Arg249 and Asn253) were most effective at relieving inhibition, especially W203A, which restored the full GEF activity of ASEF toward CDC42 in vitro. The equivalent mutation (W156A) in ASEF2 ΔN is also activating (Fig. 7b, right graph), indicating that ASEF and ASEF2 are similarly auto-inhibited by their respective SH3 domains. Consistent with these in vitro results, ASEF ΔABR4 W203A and a constitutively active ASEF DH/PH protein induced filopodia formation to a similar degree in NIH3T3 cells (Fig. 7c).

ASEF is a candidate tumor suppressor

To better understand the regulation of ASEF by APC in CRCs, we suppressed the expression of ASEF by RNA interference in CRC cell lines that retain full-length (SW48 and HCT116) or truncated (SW480) APC31,32 and assessed CDC42 activation and tumorigenic potential. We established individual cell lines stably expressing each of two independent short hairpin RNAs (shRNA-1 and shRNA-2) targeting ASEF or a nontargeting control (shRNA-C) and assessed the amount of GTP-bound CDC42 by affinity precipitation. Knockdown of ASEF messenger RNA in SW48 and HCT116 cell lines harboring full-length APC led to decreased levels of CDC42-GTP (Fig. 8a). In contrast, the amount of CDC42-GTP remained unchanged in SW480 cells despite depletion of ASEF mRNA.

Figure 8
ASEF is a candidate tumor suppressor

The HCT116 and SW480 cell lines expressing shRNAs were also assessed for anchorage-independent growth in soft agar (Fig. 8b; SW48 cells grow poorly in soft agar). HCT116 cells expressing ASEF-specific shRNAs showed a two- to four-fold increase in anchorage-independent growth compared to cells expressing control shRNA, whereas colony growth of SW480 cells was not affected by ASEF knockdown. Notably, in both cell types, anchorage-independent growth was promoted by expression of a dominant-negative form of CDC42 fused to a hemag-glutinin tag (HA–CDC42 17N), which forms a nonproductive complex with CDC42-specific GEFs and suppresses their activity33. These data suggest that full-length APC promotes the activation of CDC42 by ASEF to suppress the anchorage-independent growth of HCT116 cells. In SW480 cells expressing truncated APC that does not activate ASEF, CDC42-GTP levels remained high and no enhancement of anchorage-independent growth was observed upon ASEF knockdown.

ASEF has recently been found to be mutated in human cancers34 and designated as a candidate cancer gene predicted to have higher-than-background mutation frequencies in cancers. Two separate missense mutations of ASEF have been uncovered in breast cancers: K100R in the N terminus and T441R in the DH domain. In our structure of ASEF, Thr441 resides in the turn separating α5 and α6, where it participates in an extensive network of hydrogen bonds with residues in α1, α3, α5 and α6 to stabilize the DH domain fold (Fig. 8c). Substitution of arginine for Thr441 would disrupt these interactions and would probably be very detrimental to the overall fold and associated exchange activity of the DH domain. Consistent with this assumption, T441R mutation in the constitutively active ASEF DH/PH protein abolished its ability to promote ruffling in COS-7 cells and abolished the activation of ASEF ΔABR2 by APCArm in fluorescence-based GEF assays (Fig. 8d). Therefore, we conclude that the T441R mutation in ASEF causes loss of the GEF activity of ASEF and thereby leads to loss of regulation of CDC42 by APC. Together, these data imply that loss of ASEF function is advantageous to tumor progression and that ASEF acts as a tumor suppressor.


There are approximately 70 Dbl-family RhoGEFs that differentially activate 20 Rho GTPases in humans. Although the ASEF-related GEFs collybistin6,28 and ASEF2 (ref. 7) are specific for CDC42, the specificity of ASEF for Rho GTPases has been controversial. Initial reports indicated that ASEF was a RAC1-specific GEF8,9,29, whereas a recent study18 showed that ASEF was specific for CDC42 and not RAC1. Consistent with that study, our data demonstrate that ASEF acts as a CDC42 GEF in vitro and in vivo and does not activate other Rho GTPases. Notably, knockdown of ASEF in CRC cell lines expressing full-length APC decreases the levels of GTP-bound CDC42. This clarification of ASEF specificity is biologically relevant, as RAC1 and CDC42 regulate distinct cellular processes35.

The structure of autoinhibited ASEF reveals that the SH3 domain forms a unique interface with regions in both the DH and PH domains and masks the surface on the DH domain (α1, α5 and α6) required for binding Rho GTPases during nucleotide exchange. This steric occlusion inhibits the GEF activity of ASEF. The CAB motif and the remainder of the ABR are largely solvent exposed and not part of the inhibitory interface. Therefore, truncated forms of ASEF that lack the ABR but retain the SH3 domain are constitutively inhibited, and previous studies that have used such forms of ASEF and assumed their constitutive activation should be reinterpreted. Mutations in the SH3 domain (R249A and N253A) that enhance the exchange activity of full-length ASEF without perturbing the capacity of the SH3 domain to bind polyproline-containing ligands could be used in place of truncated forms of ASEF in future studies.

Recently, a different mechanism for ASEF2 autoinhibition has been put forth, in which interactions between the ABR and SH3 domains and regions on the C-terminal side of the PH domain are important for its autoinhibition7. However, for both ASEF and ASEF2, we find that removal of the C-terminal region following the PH domain does not influence the exchange potential of these GEFs (see Supplementary Fig. 5 online). Furthermore, substitutions in the SH3 domain of ASEF designed to disrupt its interaction with the DH and PH domains, as well as analogous substitutions in ASEF2, activate the respective exchange potentials of these GEFs, indicating that our proposed mechanism of autoinhibition of ASEF is almost certainly conserved in ASEF2.

It is becoming clear that APC is involved in the regulation of several cellular processes independent of its role in Wnt signaling, including the reorganization and stabilization of the cytoskeleton and regulation of cell migration, cell division and apoptosis4. It is increasingly appreciated that truncated forms of APC associated with cancers might have differential activities that promote tumorigenesis independently of the loss of β-catenin regulation. ASEF is reported to have a crucial role in cellular migration downstream of truncated APC9. We show here that truncation of APC leads to the loss of ASEF function. Truncated APC does not promote morphological changes associated with ASEF and CDC42 activation, probably owing to the altered cellular localization of truncated APC. The coupling of APC to CDC42 activation via ASEF that we observed in CRC cell lines expressing full-length APC is lost upon APC truncation. Moreover, suppression of ASEF in CRC cells expressing full-length APC greatly increases anchorage-independent growth of these cells, whereas colony growth is not affected by ASEF knockdown in cells expressing truncated APC. These data support a mechanism in which ASEF signals downstream of full-length APC to activate CDC42 to suppress anchorage-independent growth. Notably, dominant-negative CDC42 enhances anchorage-independent growth of CRC cell lines expressing either full-length or truncated APC, demonstrating that the general loss of CDC42 activity by sequestration of GEFs can promote CRC.

ASEF has recently been found to be mutated in human breast cancers and not in CRCs34. In one breast tumor, ASEF acquired a homozygous mutation at codon 441 (T441R)36 that abolishes catalytic activity (Fig. 8d), suggesting that ASEF acts as a tumor suppressor in breast epithelial cells. Together with our findings in CRC cell lines, these data strongly imply that the loss of ASEF function is advantageous to tumor progression in general and that ASEF is a tumor suppressor in multiple cell types. Given that APC is not typically mutated in breast cancers, and ASEF mutations have not been found in CRCs, it is possible that loss of ASEF function can be achieved indirectly through mutation of APC (in CRCs) or by direct mutation and inactivation of ASEF (in breast cancers). The consequence of regulation of CDC42 by APC and ASEF and the role of CDC42 itself in cancer progression are not known. Future studies will determine the signaling pathways mediated by ASEF and uncover the roles of ASEF and CDC42 in human cancers.


Protein expression and purification

His6-tagged ASEF and ASEF2 (human) proteins were expressed in Rosetta BL21(DE3) Escherichia coli cells. To produce selenomethionine (SeMet)-substituted ASEF ΔABR2 for structure determination, ASEF ΔABR2 was expressed using the methionine-auxotrophic E. coli strain B834(DE3) and cultured in L-SeMet–enriched media using methods similar to those described37. Detailed descriptions of protein expression and purification are available in the Supplementary Methods. APCArm proteins (human, residues 309–798) were purified exactly as described for ASEF proteins, except all buffers contained 500 mM NaCl and EDTA was not included in buffer B.

Human placental CDC42 (residues 1–188; C188S), RAC1 (residues 1–189; C189S) and RHOA (residues 1–190; C190S) were expressed in E. coli strain BL21(DE3) and purified as described13. His6-tagged Rho GTPases used in Supplementary Figure 1 were prepared as described38.

Guanine nucleotide exchange assays

N-methylanthraniloyl (mant)-GTP incorporation into bacterially purified Rho GTPases was carried out with a Perkin-Elmer LS 55 spectrometer at 20 °C. Exchange-reaction assay mixtures containing 20 mM Tris (pH 7.5), 100 mM NaCl, 5 mM MgCl2, 1 mM DTT, 5% (v/v) glycerol, 400 nM mant-GTP (Molecular Probes) and 2 µM of the relevant GTPase were prepared and allowed to equilibrate with continuous stirring. After equilibration, ASEF or ASEF2 proteins were added at 1 µM, and the relative fluorescence (λemission = 360 nm, λexcitation = 440 nm) was monitored. For experiments including APCArm, we incubated ASEF or ASEF2 proteins on ice with APCArm for 10 min before adding them to GEF reactions. The final concentration of APCArm in GEF reactions was 1 µM.

Immunostaining and fluorescence microscopy

For live-cell microscopy, NIH3T3 and COS-7 cells were plated, transfected and imaged in 35-mm MatTek culture dishes. Plates were mounted 16–24 h after transfection on a temperature-controlled heated stage (TempControl 37-2 digital, Carl Zeiss MicroImaging), and live cells were examined with an inverted laser scanning confocal microscope (Zeiss 510 LSM) using an oil-immersion ×63 NA 1.4 objective. For studies of mCherry-ASEF colocalization with GFP-APC, images were captured by sequential scanning with the 488-nM spectral line of an argon ion laser and the 543-nM HeNe1 laser and emission filters BP 505–530 (for GFP) and LP 585 (for mCherry).

For indirect immunofluorescence, NIH3T3 cells were plated and transiently transfected in four-well Lab-Tek chambered glass coverslides (Nunc). The next day, cells were fixed with 4% (v/v) paraformaldehyde, permeabilized with 0.2% (v/v) Triton X-100 and stained with Alexa 594–phalloidin (Molecular Probes). Cells were mounted with FluoroSave (Calbiochem) and examined with a Zeiss 510 LSM confocal microscope. Digital images were processed and brightness and contrast adjusted with Adobe Photoshop CS2.

Crystallization of ASEF

SeMet-substituted ASEF ΔABR2 was crystallized by vapor diffusion in sitting drops. Drops were formed by a 2:1 ratio of protein solution (~9mg ml−1 in buffer B) to reservoir solution (100 mM HEPES (pH 7), 20% (w/v) PEG 3,350, 200 mM magnesium acetate and 10% (v/v) glycerol), then equilibrated against 1 ml of reservoir solution at 18 °C. Reproducibility and crystal quality were generally improved by microcrystal seeding. For data collection at 100 K, crystals were suspended in a rayon loop (Hampton Research) and snap-frozen by immersion into liquid nitrogen. Crystals belong to the space group C2, with unit cell dimensions of a = 116.4, b = 80.5, c = 101.5 and β = 104.5°. There are two apparent monomers in the asymmetric unit. A three-wavelength MAD data set (λ1 = 12,661.14 eV, λ2 = 12,659.14 eV, λ3 = 12,760.14 eV) was collected on a single crystal on the Southeast Regional Collaborative Access Team (SER-CAT) beamline 22-ID at the Advanced Photon Source of Argonne National Laboratory.

A native data set was subsequently collected at the University of North Carolina X-ray facility on a single crystal at 100 K using an R-AXIS IV++ area detector and a Rigaku RU-H3R rotating anode X-ray source equipped with focusing optics. Crystals were produced from native protein as described for SeMet-substituted ASEF ΔABR2, then incubated in a soaking solution containing 100 mM HEPES (pH 7), 50% (w/v) PEG 3,350, 200 mM magnesium acetate and 10% (v/v) glycerol. Soaked crystals had unit cell dimensions of a = 100.4, b = 79.9, c = 67.4 and β = 123.0°, with one molecule in the asymmetric unit. All data were processed and scaled using HKL2000 (ref. 39).

Model building and refinement

The Patterson peak-searching program SHELXD40 and the three-wavelength MAD dataset were initially used to determine the positions of two sets of eight selenium atoms related by two-fold noncrystallo-graphic symmetry. The positions of the heavy atom sites were refined using the CCP4 program MLPHARE41 before phase improvement with solvent flattening, histogram matching and noncrystallographic symmetry averaging using DM42 The resulting electron density map was used for initial model building; however, density for the PH domain was almost entirely missing and further refinement gave poor statistics (Rfree > 35). Data collected on the native crystal were phased by molecular replacement with the CCP4 program PHASER43 using the best monomer model that resulted from MAD experiments. The resulting density map was of high quality and easily interpretable (Supplementary Fig. 3). The structure of ASEF ΔABR2 was completed using native protein data and iterative cycles of model building and TLS refinement with COOT44 and the CCP4 program REFMAC45. The final model has a crystallographic R-value of 21.7% (Rfree = 27.9%) using all data from 15–2.25 Å (see Table 1) and includes residues 181–254 and 278–611 of ASEF. Electron density was uninterpretable for residues 170–180 (N terminus), 255–277 (SH3-DH linker) and 612–632 (C terminus) and therefore could not be modeled. Owing to the poor electron density in this region, residues 561–570 (in the β5–β6 loop of the PH domain) were modeled as glycines. In the Ramachandran plot, 91.8% of residues are in the most favored regions, 7.3% are in the allowed region and 0.8% are in the disallowed region. All molecular graphics were generated with PyMOL (http://pymol.sourceforge.net).

Table 1
Data collection, phasing and refinement statistics

CDC42 affinity precipitation assays

SW48, SW480 and HCT116 cells stably expressing control or ASEF-specific shRNAs were lysed in lysis buffer (50 mM Tris (pH 7.5), 150 mM NaCl, 10 mM MgCl2, 1% (v/v) Nonidet P-40, 0.25% (w/v) sodium deoxycholate and 10% (v/v) glycerol) plus protease inhibitor cocktail (Roche). Glutathione S-transferase (GST)-PAK RBD (see Acknowledgments) immobilized on glutathione–Sepharose 4B beads was added to clarified total cell lysates and incubated at 4 °C for 45 min. Beads were pelleted and washed once with lysis buffer and twice with wash buffer (25 mM Tris (pH 7.5), 40 mM NaCl, 30 mM MgCl2). Total lysate and affinity-precipitated lysate samples were subjected to SDS-PAGE and analyzed by western blotting using CDC42-specific antibodies (Santa Cruz Biotechnology).

Statistical analysis

Data was obtained from three independent experiments done in triplicate and P-values were calculated using a one-tailed Student’s t-test. Significance for all tests was assumed at P < 0.001 (confidence interval 95%).

Additional methods

A detailed description of expression and RNA interference constructs, maintenance of cell lines, reverse-transcription PCR and soft-agar assays is available in the Supplementary Methods.

Supplementary Material

Asef supplemen

Note: Supplementary information is available on the Nature Structural & Molecular Biology website.


We thank D. Thiel and L. Bauer for technical assistance, Keith Burridge, (University of North Carolina) for the gift of GST-PAK RBD, the M. Hooker imaging facility at the University of North Carolina, Chapel Hill, and the staff at the SER-CAT beamlines for help with data collection. Use of the Advanced Photon Source was supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, under contract no. W-31-109-Eng-38. J.S. is supported by grants GM65533 and GM62299 from the US National Institutes of Health. C.J.D. is supported by grant CA063071 from the US National Institutes of Health. K.L.R. is supported by postdoctoral fellowship grant PF-05-129-01(GMC) from the American Cancer Society.


Accession codes. Protein Data Bank: Coordinates and structure factors have been deposited with accession code 2PZ1.


The authors declare no competing financial interests.

Reprints and permissions information is available online at http://npg.nature.com/reprintsandpermissions


1. Fodde R, Smits R, Clevers H. APC, signal transduction and genetic instability in colorectal cancer. Nat. Rev. Cancer. 2001;1:55–67. [PubMed]
2. Polakis P. The adenomatous polyposis coli (APC) tumor suppressor. Biochim. Biophys. Acta. 1997;1332:F127–F147. [PubMed]
3. Segditsas S, Tomlinson I. Colorectal cancer and genetic alterations in the Wnt pathway. Oncogene. 2006;25:7531–7537. [PubMed]
4. Hanson CA, Miller JR. Non-traditional roles for the Adenomatous Polyposis Coli (APC) tumor suppressor protein. Gene. 2005;361:1–12. [PubMed]
5. Rossman KL, Der CJ, Sondek J. GEF means go: turning on RHO GTPases with guanine nucleotide-exchange factors. Nat. Rev. Mol. Cell Biol. 2005;6:167–180. [PubMed]
6. Reid T, Bathoorn A, Ahmadian MR, Collard JG. Identification and characterization of hPEM-2, a guanine nucleotide exchange factor specific for CDC42. J. Biol. Chem. 1999;274:33587–33593. [PubMed]
7. Hamann MJ, Lubking CM, Luchini DN, Billadeau DD. Asef2 functions as a CDC42 exchange factor and is stimulated by the release of an autoinhibitory module from a concealed C-terminal activation element. Mol. Cell. Biol. 2007;27:1380–1393. [PMC free article] [PubMed]
8. Kawasaki Y, et al. Asef, a link between the tumor suppressor APC and G-protein signaling. Science. 2000;289:1194–1197. [PubMed]
9. Kawasaki Y, Sato R, Akiyama T. Mutated APC and Asef are involved in the migration of colorectal tumour cells. Nat. Cell Biol. 2003;5:211–215. [PubMed]
10. Worthylake DK, Rossman KL, Sondek J. Crystal structure of RAC1 in complex with the guanine nucleotide exchange region of Tiam1. Nature. 2000;408:682–688. [PubMed]
11. Gao Y, Xing J, Streuli M, Leto TL, Zheng Y. Trp(56) of rac1 specifies interaction with a subset of guanine nucleotide exchange factors. J. Biol. Chem. 2001;276:47530–47541. [PubMed]
12. Karnoub AE, et al. Molecular basis for RAC1 recognition by guanine nucleotide exchange factors. Nat. Struct. Biol. 2001;8:1037–1041. [PubMed]
13. Cheng L, et al. RhoGEF specificity mutants implicate RhoA as a target for Dbs transforming activity. Mol. Cell. Biol. 2002;22:6895–6905. [PMC free article] [PubMed]
14. Snyder JT, et al. Structural basis for the selective activation of Rho GTPases by Dbl exchange factors. Nat. Struct. Biol. 2002;9:468–475. [PubMed]
15. Nobes CD, Hall A. Rho, rac, and cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia, and filopodia. Cell. 1995;81:53–62. [PubMed]
16. Nobes CD, Hall A. Rho GTPases control polarity, protrusion, and adhesion during cell movement. J. Cell Biol. 1999;144:1235–1244. [PMC free article] [PubMed]
17. Thiesen S, Kubart S, Ropers HH, Nothwang HG. Isolation of two novel human RhoGEFs, ARHGEF3 and ARHGEF4, in 3p13-21 and 2q22. Biochem. Biophys. Res. Commun. 2000;273:364–369. [PubMed]
18. Gotthardt K, Ahmadian MR. Asef is a CDC42-specific guanine nucleotide exchange factor. Biol. Chem. 2007;388:67–71. [PubMed]
19. Nalbant P, Hodgson L, Kraynov V, Toutchkine A, Hahn KM. Activation of endogenous CDC42 visualized in living cells. Science. 2004;305:1615–1619. [PubMed]
20. Kins S, Betz H, Kirsch J. Collybistin, a newly identified brain-specific GEF, induces submembrane clustering of gephyrin. Nat. Neurosci. 2000;3:22–29. [PubMed]
21. Nathke I. Cytoskeleton out of the cupboard: colon cancer and cytoskeletal changes induced by loss of APC. Nat. Rev. Cancer. 2006;6:967–974. [PubMed]
22. Munemitsu S, et al. The APC gene product associates with microtubules in vivo and promotes their assembly in vitro. Cancer Res. 1994;54:3676–3681. [PubMed]
23. Rosin-Arbesfeld R, Ihrke G, Bienz M. Actin-dependent membrane association of the APC tumour suppressor in polarized mammalian epithelial cells. EMBO J. 2001;20:5929–5939. [PMC free article] [PubMed]
24. Kurokawa K, Itoh RE, Yoshizaki H, Nakamura YO, Matsuda M. Coactivation of RAC1 and CDC42 at lamellipodia and membrane ruffles induced by epidermal growth factor. Mol. Biol. Cell. 2004;15:1003–1010. [PMC free article] [PubMed]
25. Watanabe T, et al. Interaction with IQGAP1 links APC to RAC1, CDC42, and actin filaments during cell polarization and migration. Dev. Cell. 2004;7:871–883. [PubMed]
26. Smith KJ, et al. Wild-type but not mutant APC associates with the microtubule cytoskeleton. Cancer Res. 1994;54:3672–3675. [PubMed]
27. Li SS. Specificity and versatility of SH3 and other proline-recognition domains: structural basis and implications for cellular signal transduction. Biochem. J. 2005;390:641–653. [PMC free article] [PubMed]
28. Xiang S, et al. The crystal structure of CDC42 in complex with collybistin II, a gephyrin-interacting guanine nucleotide exchange factor. J. Mol. Biol. 2006;359:35–46. [PubMed]
29. Murayama K, et al. Crystal structure of the rac activator, Asef, reveals its autoinhibitory mechanism. J. Biol. Chem. 2007;282:4238–4242. [PubMed]
30. Soisson SM, Nimnual AS, Uy M, Bar-Sagi D, Kuriyan J. Crystal structure of the Dbl and pleckstrin homology domains from the human Son of sevenless protein. Cell. 1998;95:259–268. [PubMed]
31. Morin PJ, et al. Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC. Science. 1997;275:1787–1790. [PubMed]
32. El-Bahrawy M, Poulsom R, Rowan AJ, Tomlinson IT, Alison MR. Characterization of the E-cadherin/catenin complex in colorectal carcinoma cell lines. Int. J. Exp. Pathol. 2004;85:65–74. [PMC free article] [PubMed]
33. Feig LA. Tools of the trade: use of dominant-inhibitory mutants of Ras-family GTPases. Nat. Cell Biol. 1999;1:E25–E27. [PubMed]
34. Sjoblom T, et al. The consensus coding sequences of human breast and colorectal cancers. Science. 2006;314:268–274. [PubMed]
35. Etienne-Manneville S, Hall A. Rho GTPases in cell biology. Nature. 2002;420:629–635. [PubMed]
36. Knudson AG. Two genetic hits (more or less) to cancer. Nat. Rev. Cancer. 2001;1:157–162. [PubMed]
37. Doublie S. Preparation of selenomethionyl proteins for phase determination. Methods Enzymol. 1997;276:523–530. [PubMed]
38. Snyder JT, Singer AU, Wing MR, Harden TK, Sondek J. The pleckstrin homology domain of phospholipase C-beta2 as an effector site for Rac. J. Biol. Chem. 2003;278:21099–21104. [PubMed]
39. Otwinowski Z, Minor W. Processing of x-ray diffraction data collected in oscillation mode. Methods Enzymol. 1997;276:307–326.
40. Sheldrick GM. SHELXS86-Program for Crystal Structural Solution. Germany: University of Gottingen; 1986.
41. Collaborative Computational Project, Number 4. The CCP4 suite: programs for protein crystallography. Acta Crystallogr. D Biol. Crystallogr. 1994;50:760–763. [PubMed]
42. Cowtan KD. DM: an automated procedure for phase improvement by density modification. Joint CCP4 ESF-EACBM Newsl. Protein Crystallogr. 1994;31:34–38.
43. McCoy AJ, Grosse-Kunstleve RW, Storoni LC, Read RJ. Likelihood-enhanced fast translation functions. Acta Crystallogr. D Biol. Crystallogr. 2005;61:458–464. [PubMed]
44. Emsley P, Cowtan K. Coot: model-building tools for molecular graphics. Acta Crystallogr. D Biol. Crystallogr. 2004;60:2126–2132. [PubMed]
45. Murshudov GN, Vagin AA, Dodson EJ. Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallogr. D Biol. Crystallogr. 1997;53:240–255. [PubMed]
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