INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

Expression of the protein tyrosine kinase encoded by the v-abl oncogene of Abelson murine leukemia virus (Ab-MLV) induces transformation of pre-B cells and immortalized fibroblast lines in vitro and causes pre-B-cell lymphoma in mice (37). Although the tyrosine kinase activity of the v-Abl protein is absolutely required for transformation, the SH2 domain, a region involved in phosphotyrosine-dependent interactions (11, 48), also plays an important role in the process. This domain contains a phosphotyrosine-binding pocket characterized by the amino acids FLVRES; replacing Arg B5, located at the base of the pocket, with a Lys or other residues drastically affects the ability of activated c-Abl proteins and Bcr/Abl proteins to transform immortalized fibroblast lines (1, 28). These substitutions drastically reduce binding of tyrosine-phosphorylated peptides to SH2 domains; those affecting other pocket residues have more modest effects on binding and variable effects on transformation mediated by Abl or by Src, which has a closely related SH2 domain (3-5, 13, 28, 44, 47).

Although the FLVRES motif and Arg B5 play a dominant role in SH2-mediated phosphopeptide binding, they do not fully account for the specificity of SH2 domain substrate interaction. Residues within the SH2 domain that contact residues C terminal to the phosphotyrosine on the target protein are one way in which specificity of substrate interaction may be controlled (26, 43). However, analyses of interactions between Src SH2 domain mutants and peptides deviating from its consensus pYEEI peptide binding sequence have suggested that specificity reflects more complex interactions (5). Parameters such as intracellular location (which likely affects the proximity of the kinase and particular substrates), the ability to assemble signaling complexes, and interactions with other domains of the kinase are likely to influence substrate selection and play a role in SH2 domain function.

Identifying substrates that interact with SH2 domains and probing the way these interactions contribute to transformation provide one approach to understanding how SH2-mediated signaling specificity contributes to host-virus interaction. For the v-Abl protein, the Shc adapter molecule is one such substrate (31, 35). Shc can complex with Grb2 and the G-protein exchange factor, mSos, facilitating the activation of Ras (14, 27). The last event is required for Abl-mediated transformation (39). Activation of Ras stimulates multiple downstream effector proteins, including c-Myc (21-23), another protein that is critical for Abl-mediated transformation (38). Consistent with the idea that signals requiring an intact SH2 domain pass through Ras and lead to c-Myc (52), transformation of RAT-1 cells by Bcr/Abl proteins containing an altered FLVRES motif is complemented by expression of c-Myc (1, 25).

To understand how the v-Abl SH2 domain contributes to transformation and downstream signaling, we examined the biological properties of the P120/R273K mutant. This mutant encodes a v-Abl protein in which a Lys is substituted for Arg B5. Unexpectedly, P120/R273K retained significant transformation potential when assayed at 34°C but was compromised for transformation at 39.5°C. These defects were correlated to deficiencies in interactions with Shc and decreased stimulation of c-Myc. These data reveal a novel type of Ab-MLV temperature-sensitive (ts) mutant and a previously unappreciated effect of temperature on v-Abl proteins with an altered SH2 domain.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Cells and viruses. NIH 3T3 cells were grown in Dulbecco's modified Eagle's medium supplemented to contain 10% calf serum (Sigma); Ab-MLV-transformed NIH 3T3 cells and 293T cells (15) were grown in Dulbecco's modified Eagle's medium supplemented to contain 10% fetal calf serum (Intergen). Ab-MLV-transformed pre-B-cell lines were grown in RPMI 1640 medium supplemented to contain 20% fetal calf serum and 50 µM 2-mercaptoethanol (Sigma). The ts Ab-MuLV-transformed pre-B-cell line 7C411 was derived by infecting bone marrow cells with the ts Ab-MuLV strain P70/H590 (17) and maintained at 34°C, the permissive temperature for the ts Ab-MuLV mutants; the nonpermissive temperature used was 39.5°C. Retroviral stocks were prepared using transient transfection of 293T cells as described elsewhere (49). The pSR-MSVtkneo vector (30) or the pMIG vector (19, 46) was used to express the different Ab-MLV strains. In the pMIG vector, green fluorescent protein (GFP) expression is mediated by an internal ribosome entry site (IRES) sequence and gag/v-abl sequences are cloned upstream of the IRES sequence. Infectivity was evaluated by Western blot analysis of the levels of v-Abl protein in lysates of NIH 3T3 cells that had been infected for 48 to 72 h with the Ab-MLV stocks prepared with the pSR vector (33) or by using fluorescence-activated cell sorting (FACS) to score the frequency of GFP-positive NIH 3T3 cells 24 h after infection with Ab-MLV stocks prepared using the pMIG vector. The titers of virus were also determined using the NIH 3T3 cell transformation assay (40). Bone marrow transformation assays were done as described previously (36). Macroscopic pre-B-cell colonies were counted 10 to 12 days later. For some assays, the infected cells were plated directly into RPMI 1640 medium supplemented to contain 20% fetal calf serum and 50 µM 2-mercaptoethanol. Cultures were scored as transformed when the number of nonadherent pre-B cells exceeded 2 × 10⁶ per ml of culture medium (1, 29). To obtain derivatives of 7C411 cells expressing wild-type or Ab-MLV mutants, 10⁶ cells were infected in the presence of 4 µg of Polybrene per ml for 4 h and plated in standard growth medium; 24 h later, 1 mg of G418 per ml was added to the medium to select for cells expressing the superinfecting virus, and the cells were plated in 96-well plates. Individual clones of G418-resistant cells were isolated 7 to 14 days later. Cell cycle parameters were monitored by analyzing propidium iodide-stained cells using a FACScan and Modfit LT software (8).

Construction of viral strains. pSR-P120 and the kinase negative mutant P120/D484N have been described elsewhere (35, 49). The P120/R273K mutant was created by PCR using pUC120 as a template (18) and one primer which changed the codon for Arg-273 to a Lys codon. The fragment containing the mutation was subcloned and then shuttled into pSR-P120 as a BstEII-DraIII (bases 725 to 2111 of the P120 genome) fragment. Ab-MLV P120 and P120/R273K were introduced into pMIG by shuttling the viral sequences contained on an EcoRI fragment from the pSR vectors into the EcoRI cloning site of pMIG (19, 46). The presence of all mutations and the integrity of all sequences derived by PCR amplification were examined in the DNA Facility, Department of Physiology, Tufts University School of Medicine.

Protein analysis. Cells were treated with lysis buffer (10 mM Tris [pH 7.4], 1% sodium dodecyl sulfate [SDS], 1 mM sodium orthovanadate, 1 mM phenylmethylsulfonyl fluoride [PMSF]) as described previously (9, 32). Protein was quantitated using a bicinchoninic acid protein assay kit (Pierce), and 50 µg of each sample was fractionated through SDS-polyacrylamide gels. The proteins were transferred to a polyvinylidene difluoride membrane (U.S. Biochemicals), and the blots were treated according to the Western-Light kit protocol (Tropix) using alkaline phosphatase-conjugated secondary antibodies and the CSPD substrate (Tropix). For immunoprecipitation with anti-p62 Dok antibodies, cells were resuspended in ice-cold TNN lysis buffer (150 mM NaCl, 50 mM Tris [pH 8], 1% NP-40, 10 µg of leupeptin per ml, 1 mM orthovanadate, and 1 mM PMSF); for immunoprecipitation with anti-Shc antibodies, cells were resuspended in radioimmunoprecipitation assay buffer (10 mM sodium phosphate [pH 7], 150 mM NaCl, 0.1% SDS, 50 mM NaF, 1% NP-40, 0.5% sodium deoxycholate, 2 mM EDTA, 1 mM sodium orthovanadate, 1 mM PMSF, and 10 µg of leupeptin per ml). The lysates were clarified and equivalent amounts of protein were immunoprecipitated. The immune complexes were recovered with Sepharose CL-4B beads and heated at 95°C for 5 min. The proteins were resolved on SDS-polyacrylamide gels and analyzed by immunoblotting. In some experiments, fusion proteins in which SH2 domains fused to glutathione S-transferase (GST) were used to precipitate proteins. The GST-SH2 proteins were produced by using the pGEX-3X vector (Pharmacia) and Escherichia coli JM109 cells and reacted with cell lysates as described previously (35). Immunofluorescent staining for v-Abl was carried out using cells fixed with 1% formaldehyde and the anti-v-Abl monoclonal antibody 24-21 (41). Proteins were analyzed using anti-Gag/v-Abl (H548) (10), anti-Shc (S14630; Transduction Laboratories), anti-Grb2 (G16720; Transduction Laboratories), anti-p62 Dok (MMS239P [Babco] or SC6929 [Santa Cruz Biotechnology]), anti-myc (06-340; Upstate Biotechnology), antiphosphotyrosine (05-321; Upstate Biotechnology), anti-p42/p44 MAPK (9100; New England Biolabs), and anti-GST (SC-138; Santa Cruz Biotechnology) antibodies. Control antibodies included rabbit gamma globulin, anti--2-6 fructosan (UPC-10) (2), and anti-murine immunoglobulin ( chain).

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Alteration of the v-Abl SH2 domain reduces NIH 3T3 cell transformation in a temperature-dependent fashion. To determine the effects of an altered v-Abl SH2 domain on Ab-MLV transformation, NIH 3T3 cells were infected with the Ab-MLV P120/R273K mutant and monitored for transformation. Ab-MLV P120- or mock-infected cells served as controls. Cells were examined at the standard 37°C used by others for analogous mutants in other forms of Abl and at 34 and 39.5°C, temperatures commonly used with mammalian cells and ts mutants. When cells infected and maintained at 34°C were compared to sister cultures infected at 34°C and then shifted to 39.5°C for 48 h, similar levels of v-Abl proteins were recovered (Fig. 1). All of the extracts contained elevated levels of phosphotyrosine compared to those of mock-infected cells (Fig. 1). Although these levels were reduced in cells infected with P120/R273K and maintained at 34°C, the reductions were more obvious when the cells were maintained at 39.5°C. Effects on some proteins (Fig. 1) were more striking, suggesting that temperature may affect the ability of certain substrates to interact with P120/R273K. In addition, tyrosine phosphorylation of P120/R273K itself was also reduced.

View larger version (68K): [in this window] [in a new window]   FIG. 1.   Cells expressing P120/R273K contain low levels of phosphotyrosine at high temperature. NIH 3T3 cells were infected with Ab-MLV P120 or P120/R273K or were mock infected at 34°C (L); some samples were then shifted to 39.5°C (H), and all were lysed 48 h later. Equivalent amounts of total cellular protein were analyzed by using Western blotting with antiphosphotyrosine antibodies or the anti-Gag/v-Abl monoclonal antibody H548 (10). Molecular weight standards (in thousands) are indicated on the left, and arrows highlight bands which display temperature-dependent differences in phosphotyrosine. The asterisk indicates the v-Abl protein.

Reduced binding of Shc and p62Dok to an SH2 domain with the R273K substitution. Even though substitutions affecting the conserved Arg in the FLVRES motif dramatically reduce the ability of SH2 domains to interact with tyrosine-phosphorylated peptides (3-5, 28), P120/R273K is only mildly compromised for NIH 3T3 cell transformation at 34°C. These data could suggest that SH2 domain interactions in vivo are more complex than can be detected by in vitro binding assays. To explore this hypothesis, the ability of the R273K SH2 domain to bind two v-Abl substrates, Shc and p62Dok, was tested by using GST-SH2 fusion proteins. Shc transmits stimulatory signals via the Grb2-Sos complex to Ras after tyrosine phosphorylation by v-Abl (14, 27, 31, 35); tyrosine-phosphorylated p62Dok is believed to stimulate Ras by binding the Ras suppressor p120RasGap (7, 16, 51).

View larger version (29K): [in this window] [in a new window]   FIG. 2.   Shc and p62Dok bind poorly to an SH2 domain with the R273K substitution. (A) Lysates of uninfected NIH 3T3 cells or cells transformed with Ab-MLV P120 were incubated with GST alone, GST-SH2, or GST-R273K SH2. The proteins were recovered and analyzed by using Western blotting with an anti-Shc antibody. (B) Lysates of NIH 3T3 cells transformed by Ab-MLV P120 were incubated with the indicated GST-SH2 domain fusion proteins or GST protein as a control. The recovered proteins were analyzed by using Western blotting with an anti-p62Dok antibody. All samples contained equivalent amounts of GST proteins (data not shown).

Temperature-dependent transformation correlates to decreased signals to the Ras pathway intermediates. The discrepancy between the in vitro binding data and the transforming potential of P120/R273K at 34°C suggests that the binding experiments may not fully reveal the signaling potential of the altered v-Abl protein. To explore this issue in vivo, we examined tyrosine phosphorylation of Shc and p62Dok in NIH 3T3 cells infected with the mutant and maintained at 34 and 39.5°C. Immunoprecipitation and Western analysis revealed that NIH 3T3 cells infected 48 h previously and incubated at 34 and 39.5°C expressed similar levels of Shc, p62Dok, and v-Abl (Fig. 3 and 4). However, tyrosine phosphorylation of these two proteins was affected differently in the presence of P120/R273K at the two incubation temperatures. Tyrosine phosphorylation of Shc was decreased about fourfold in cells infected with P120/R273K at 39.5°C compared to that in cells expressing P120 or P120/R273K at 34°C (Fig. 3); association with Grb2 was more strongly affected and was reduced to levels similar to those seen in mock-infected cells. In contrast, tyrosine phosphorylation of p62Dok was slightly decreased in cells expressing P120/R273K at both incubation temperatures (Fig. 4). These results suggest that signals for activation of Shc and subsequent association of Grb2 are altered by temperature-dependent changes affecting the P120/R273K protein. Because decreases in Shc phosphorylation appear more modest than effects on Grb2 association, assessing tyrosine phosphorylation levels may not fully reflect the ability of Shc to mediate downstream signaling. However, effects on p62Dok were more modest, suggesting that alteration of the FLVRES motif has various effects on different v-Abl substrates and that some are more drastically affected by temperature than others. These data also confirm that in vitro binding does not reveal the full complexity of interactions influenced by the SH2 domain in vivo.

View larger version (38K): [in this window] [in a new window]   FIG. 3.   Tyrosine phosphorylation of Shc and Shc-Grb2 complexes are reduced in cells expressing P120/R273K at 39.5°C. NIH 3T3 cells were infected with Ab-MLV P120 or P120/R273K or were mock infected and incubated at 34°C (L) or 39.5°C (H). (A) The cells were lysed 48 h later, and a portion of the lysate was immunoprecipitated with anti-Shc antibody or rabbit gamma globulin as a control and analyzed by using Western blotting and antiphosphotyrosine, anti-Grb2, and anti-Shc antibodies. Lanes labeled "Shc" contain samples immunoprecipitated with anti-Shc antibody; lanes labeled "C" contain samples immunoprecipitated with rabbit gamma globulin. The antibodies used to probe the blots are listed to the right. (B) The remaining lysate was analyzed by using Western blotting with the anti-Gag/v-Abl monoclonal antibody H548 (10).

View larger version (35K): [in this window] [in a new window]   FIG. 4.   Tyrosine phosphorylation of p62Dok is not temperature dependent. NIH 3T3 cells were infected with Ab-MLV P120 or P120/R273K or were mock infected and incubated at 34°C (L) or 39.5°C (H), and lysates were prepared 48 h later. (A) A portion of the lysate was immunoprecipitated with anti-p62Dok or the UPC-10 control antibody (2) and analyzed by using antiphosphotyrosine and anti-p62Dok antibodies. Lanes labeled "p62" contain samples immunoprecipitated with anti-p62Dok antibody; lanes labeled "C" contain samples immunoprecipitated with UPC-10 control antibody. The antibodies used to probe the blots are listed to the right. (B) The remaining lysate was analyzed by using Western blotting with the anti-Gag/v-Abl monoclonal antibody H548 (10).

Pre-B-cell transformation by P120/R273K is temperature dependent. Some Ab-MLV mutants display different transformation phenotypes in NIH 3T3 cells and pre-B cells (37). To determine if pre-B-cell transformation by the P120/R273K mutant is also temperature dependent, primary bone marrow cells were infected, plated in agar or liquid medium (1, 29, 36) at 34, 37, and 39.5°C, and monitored for transformation. Liquid cultures were scored as transformed when the cell density exceeded approximately 2 × 10⁶ transformed cells per ml, a time at which the cells could be subcultured; for agar assays, the frequency of macroscopic colonies of primary transformants was determined 10 days postinfection. Bone marrow cells infected with Ab-MLV P120 became transformed at all temperatures, and the P120/R273K mutant transformed fewer cells under all conditions (Table 2). Between five- and sevenfold fewer colonies were observed in agar at both 34 and 37°C. However, transformation frequencies were reduced approximately 100-fold at 39.5°C, with one to two very small pre-B-cell colonies being observed; these cell populations could not be expanded. Consistent with the diminished transformation potential of the P120/R273K mutant, infected liquid cultures maintained at 34 and 37°C became transformed later than those infected with the wild-type virus. Although some pre-B cells appeared to proliferate in several cultures infected with P120/R273K and maintained at 39.5°C, the population of these cells could not be expanded. These data demonstrate that the temperature-dependent transformation response found in NIH 3T3 cells extends to pre-B cells and represents a general feature of transformation responses to P120/R273K.

Pre-B cells transformed by P120/R273K grow poorly at elevated temperature. NIH 3T3 cells transformed at 34°C maintained a transformed morphology at 39.5°C. To determine if pre-B cells transformed by P120/R273K at 34°C could grow at 39.5°C, these cells and controls transformed by wild-type P120 were shifted to the high temperature, and growth was monitored by counting viable cells using phase microscopy. Consistent with previous results (8), cells transformed by P120 grew more rapidly at 39.5 than at 34°C, while cells transformed with P120/R273K grew poorly at both temperatures (Fig. 5).

View larger version (12K): [in this window] [in a new window]   FIG. 5.   Pre-B cells transformed by P120/R273K grow poorly at 39.5°C. Bone marrow cells were transformed by Ab-MLV P120 (squares) or P120/R273K (circles) at 34°C, and primary transformants were expanded and established. Cells were counted and seeded in 35-mm dishes at a density of 105 cells per ml and incubated at 34°C (open symbols) or 39.5°C (filled symbols). Duplicate cultures were counted, and viable cells were enumerated using phase microscopy daily for 3 days. The experiments shown are representative of at least three experiments in which two or more cell lines transformed with each virus were analyzed.

Expression of c-Myc is decreased at the nonpermissive temperature. Expression of c-Myc is required for Abl-mediated transformation (38). Earlier studies, conducted at 37°C, have documented that the R273K substitution reduces the ability of v-Abl to activate expression from the E2F site in the c-myc promoter (50, 52). To determine if the temperature-dependent effects of P120/R273K affect the level of c-Myc protein expression, 7C411 cells that had been superinfected with either P120 or P120/R273K were maintained at 34°C or shifted to 39.5°C for 20 h, and lysates were prepared. Cells superinfected with the kinase-negative mutant P120/D484N (35) and parental 7C411 cells were used as controls. In a parallel experiment, pre-B cells transformed by P120 and P120/R273K at 34°C were examined at both temperatures. Western analyses revealed that c-Myc expression was diminished at 39.5°C in all of the cells expressing P120/R273K but not in those expressing P120 (Fig. 6). These data reveal that the R273K substitution affects expression of c-Myc, a critical downstream target of v-Abl (38), in a temperature-dependent fashion.

View larger version (60K): [in this window] [in a new window]   FIG. 6.   Expression of c-Myc is decreased in cells expressing P120/R273K at 39.5°C. Pre-B-cell lines transformed at 34°C by Ab-MLV P120 or P120/R273K (A) or 7C411 parental cells (P) expressing P120, P120/D484N, or P120/R273K (B) were maintained at 34°C or shifted to 39.5°C for 48 h, and lysates were prepared. The samples were analyzed via Western blotting using anti-c-Myc. The anti-Gag/v-Abl monoclonal antibody H548 (10) was used as a loading control in the top panel; anti-Erk antibody was used as a loading control in the bottom panel. In panel A, three representative pre-B-cell lines transformed with P120/R273K are shown; in panel B, two representative clones expressing P120/R273K are shown.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

These experiments identified the sequences encoding the v-Abl SH2 domain as a novel and previously unrecognized target for Ab-MLV ts mutations. The P120/R273K mutant displays a temperature-dependent transformation phenotype in both NIH 3T3 and pre-B cells. Earlier work (28) had suggested a direct correlation between the poor transformation potential of Abl proteins containing altered SH2 domains and their ability to bind tyrosine-phosphorylated molecules. However, only mild, 5- to 10-fold deficiencies are found when transformation assays are carried out at 34°C, a common permissive temperature used for conditional mutants expressed in mammalian cells. This difference is enhanced somewhat at 37°C and further magnified at 39.5°C, the temperature used for other ts Ab-MLV mutants (18). At this temperature, the effects of the mutation are particularly prominent in pre-B cells, which are refractory to transformation. These data suggest that the R273K substitution affects the structure of the phosphotyrosine-binding pocket and perhaps the entire SH2 domain in a temperature-dependent fashion.

Although temperature-dependent transformation is evident in both NIH 3T3 and pre-B-cell transformation assays, some transformed NIH 3T3 cells can be isolated at the nonpermissive temperature, and at least some cells in populations transformed at the permissive temperature retain a transformed morphology when shifted to 39.5°C. In addition, pre-B cells that have been fully transformed with P120/R273K at 34°C can replicate, albeit poorly, at 39.5°C. These data could indicate that genetic or epigenetic changes that occur during the transformation process complement transformation signals from the P120/R273K protein, allowing the emergence of transformed cells at the nonpermissive temperature once the transformation process is complete. Analyses of the pre-B-cell transformation process have revealed that inactivation of the p53 pathway is one critical step in the process (34, 45), suggesting that this event and perhaps other similar events that may occur during NIH 3T3 cell transformation affect the transforming potential of P120/R273K. The P120/R273K mutant should allow further exploration of this possibility.

Substitutions affecting Arg B5 have been studied in both Bcr/Abl and an activated, transforming c-abl allele. In both of these instances, transformation of immortalized fibroblasts is reduced by several orders of magnitude at 37°C (1, 28). However, these changes have little effect on the ability of Bcr/Abl to confer factor-independent growth on interleukin-3-dependent hematopoietic cells (12, 20, 42). Host range effects are also found in Rous sarcoma virus mutants encoding SH2 domains containing Arg B5 substitutions or with other changes in the SH2 domain (13, 44, 47). In most of these instances, transformed chick cells are fusiform, in contrast to the rounded cells induced by the wild-type virus, and immortalized rodent cells are refractory to transformation by the mutants. In two cases, large deletions removing the majority of the v-Src SH2 domain have also been shown to confer a ts phenotype (6).

Deficiencies in transformation by P120/R273K are correlated to decreased levels of phosphotyrosine on many cellular proteins, as indicated by probing whole-cell lysates with antiphosphotyrosine antibodies. Although the identity of many of these proteins is not known, one of those affected is Shc, an intermediate involved in v-Abl-mediated Ras activation (31, 35), an obligate event in the transformation process (39). However, as exemplified by p62Dok, temperature-dependent decreases in tyrosine phosphorylation are not found on all v-Abl-responsive proteins, perhaps reflecting temperature-dependent specificity in SH2-mediated interactions in the presence of the R273K substitution. Alternatively, because phosphorylation was evaluated by Western blotting, tyrosine-phosphorylated p62Dok may be more stable than the modified forms of Shc and other target proteins.

Analyses of multiple SH2 domain substitution mutants suggest that the B5 Arg residue plays the dominant role in binding of tyrosine-phosphorylated residues (3-5, 28). Consistent with these data, GST-SH2 fusions containing a Lys in place of Arg B5 interact poorly with both p62Dok and Shc in vitro. Correlations of this sort have suggested that decreases in transformation observed for some SH2 domain mutants directly reflect the inability of the transforming protein to interact with its substrates in vivo (28). Thus, it is perhaps surprising that P120/R273K retains a strong transforming potential at 34°C. However, similar substitutions affecting the v-Src SH2 domain have a limited effect on transformation, even though these clearly have large effects on peptide binding (3-5, 13, 44, 47). These data indicate that analyses of peptide interactions do not adequately reveal the potential for SH2 domains to participate in signaling when expressed in the context of the rest of the protein in an in vivo setting. Future analyses of P120/R273K may help reveal the mechanisms controlling this difference.

Study of pre-B cells transformed directly by P120/R273K at 34°C and analyses of 7C411 cells expressing P120/R273K both suggest that signals important for stimulation of growth are missing at 39.5°C. Among such signals are those which activate c-Myc, another obligate intermediate in the v-Abl transformation pathway (38). The decrease in c-Myc levels observed at 39.5°C in cells expressing P120/R273K may reflect the inability of P120/R273K to stimulate transcription dependent on the E2F site in the c-Myc promoter (50, 52). Levels of c-myc RNA are decreased in cells incubated at the high temperature (our unpublished data), suggesting that low protein levels reflect changes in expression of the gene. Activation of c-Myc expression requires an active Ras protein (52), and the decreased association of Shc and Grb2 at 39.5°C is likely to impact Ras. The ability of P120/R273K to stimulate c-Myc expression at 34 but not 39.5°C is also consistent with the temperature-dependent transformation phenotype. Thus, effects on c-Myc are likely to play a significant role in blunting the transformation response at the high temperature.

In addition to their role as docking sites for tyrosine-phosphorylated proteins, residues within SH2 domains that contact amino acids on the substrate molecules influence binding specificity (5, 43). Consistent with this idea, many mutations that map to SH2 domains confer host range effects (13, 44, 47). However, identifying the interactions that mediate these effects has been challenging. Analyses with peptides and SH2 domains with substitutions have failed to fully account for specificity (5), raising the possibility that specificity reflects the assembly of larger, multiprotein complexes which may be affected by the subcellular localization of the kinase. The ts phenotype and the stability of P120/R273K at the high temperature suggest that further analysis of interactions between this protein and cellular molecules will help illuminate the ways in which the SH2 domain contributes to Ab-MLV transformation.