Homeostasis in mRNA Initiation

Abstract

Previous kinetic binding studies of wheat germ protein synthesis eukaryotic initiation factor iso4F (eIFiso4F) and its subunit, eIF4E, with m7GTP and mRNA analogues indicated that binding occurred by a two-step process with the first step being too fast to measure by stopped-flow techniques (1Sha M. Wang Y. Xiang T. van Heerden A. Browning K. Goss D.J. J. Biol. Chem. 1995; 270: 29904-29909Abstract Full Text Full Text PDF PubMed Scopus (38) Google Scholar). Further equilibrium studies showed that poly(A)-binding protein (PABP) enhanced the cap binding of eIFiso4F about 40-fold. The kinetic effects of PABP on cap binding and the temperature dependence of this reaction were measured and compared. Fluorescence stopped-flow studies of the PABP·eIFiso4F protein complex with cap show a concentration-independent conformational change. PABP did not significantly increase the rate of the conformational change, and because the initial second-order binding is essentially diffusion-controlled, the enhancement of cap affinity must reside in the dissociation rate. The dissociation rate was more than 5-fold slower in the presence of PABP. The temperature dependence of the cap binding reaction was markedly reduced in the presence of PABP. The reduced energy barrier for formation of a cap·eIFiso4F complex suggests a more stable platform for further initiation complex formation and a possible means of adapting to varying temperature conditions. Previous kinetic binding studies of wheat germ protein synthesis eukaryotic initiation factor iso4F (eIFiso4F) and its subunit, eIF4E, with m7GTP and mRNA analogues indicated that binding occurred by a two-step process with the first step being too fast to measure by stopped-flow techniques (1Sha M. Wang Y. Xiang T. van Heerden A. Browning K. Goss D.J. J. Biol. Chem. 1995; 270: 29904-29909Abstract Full Text Full Text PDF PubMed Scopus (38) Google Scholar). Further equilibrium studies showed that poly(A)-binding protein (PABP) enhanced the cap binding of eIFiso4F about 40-fold. The kinetic effects of PABP on cap binding and the temperature dependence of this reaction were measured and compared. Fluorescence stopped-flow studies of the PABP·eIFiso4F protein complex with cap show a concentration-independent conformational change. PABP did not significantly increase the rate of the conformational change, and because the initial second-order binding is essentially diffusion-controlled, the enhancement of cap affinity must reside in the dissociation rate. The dissociation rate was more than 5-fold slower in the presence of PABP. The temperature dependence of the cap binding reaction was markedly reduced in the presence of PABP. The reduced energy barrier for formation of a cap·eIFiso4F complex suggests a more stable platform for further initiation complex formation and a possible means of adapting to varying temperature conditions. poly(A)-binding protein eukaryotic initiation factor anthraniloyl 7-methylguanosine triphosphate Most eukaryotic mRNAs contain both a 5′ cap (m7GpppX) and a 3′ poly(A) tail to increase synergistically translational efficiency and stability (2Jackson R.J. Standart N. Cell. 1990; 62: 15-24Abstract Full Text PDF PubMed Scopus (487) Google Scholar, 3Munroe D. Jacobson A. Gene. 1990; 91: 151-158Crossref PubMed Scopus (121) Google Scholar, 4Wang Z. Kiledjian M. Mol. Cell. Biol. 2000; 20: 6334-6341Crossref PubMed Scopus (86) Google Scholar). These two elements have been investigated recently, and evidence suggests that they communicate during translation (3Munroe D. Jacobson A. Gene. 1990; 91: 151-158Crossref PubMed Scopus (121) Google Scholar, 5Gallie D.R. Genes Dev. 1991; 5: 2108-2116Crossref PubMed Scopus (600) Google Scholar). These interactions are mediated by interaction of poly(A)-binding protein (PABP)1 and the cap binding complex eIF4F or an isoform of eIF4F found in plants, eIFiso4F. The small subunit of eIF4F (eIF4E) recognizes the cap structure, and the large subunit (eIF4G) interacts with PABP (6Wei C.-C. Balasta M.L. Ren J. Goss D.J. Biochemistry. 1998; 37: 1910-1916Crossref PubMed Scopus (112) Google Scholar, 7Balasta M.L. Carberry S.E. Friedland D.E. Perez R.A. Goss D.J. J. Biol. Chem. 1993; 25: 18599-18603Google Scholar). The cap-associated proteins have a very high affinity for PABP in the absence of poly(A) in the wheat germ system (8Le H. Tanguay R.L. Balasta M.L. Wei C.-C. Browning K.S. Metz A.M. Goss D.J. Gallie D.R. J. Biol. Chem. 1997; 272: 16247-16255Abstract Full Text Full Text PDF PubMed Scopus (229) Google Scholar) but require poly(A) in yeast (9Tarun Jr., S.Z. Sachs A.B. EMBO J. 1996; 15: 7168-7177Crossref PubMed Scopus (581) Google Scholar). Interaction of PABP·eIF4F has been shown to enhance the binding affinity of both cap analogs and poly(A) by about 40-fold. Further studies have shown that both the cap and poly(A) tail can be bound by the protein complex simultaneously. It was concluded that at least part of the enhancement of translation could be accounted for by increased binding affinity for the 5′ cap by the protein complex. The increase in binding affinity of the PABP·eIF4F complex for both cap analogs and poly(A) leads us to further investigate the kinetics and mechanism of these interactions. An increase in affinity for the cap structure can result from an increase in the association rate constant or a decrease in the dissociation rate constant or changes in both. Increases in the association rate constant may indicate an increase in the rate-limiting step, whereas decreases in the dissociation rate constant may indicate an increased stability for the intermediate complex in the protein synthesis pathway. We have previously investigated the mechanism of eIFiso4F or eIFiso4E interacting with cap (1Sha M. Wang Y. Xiang T. van Heerden A. Browning K. Goss D.J. J. Biol. Chem. 1995; 270: 29904-29909Abstract Full Text Full Text PDF PubMed Scopus (38) Google Scholar). Kinetic studies indicated that the binding involved a two-step process with the first reaction being too fast to measure by stopped-flow techniques. The second reaction, a conformational change, was ∼10-fold faster for eIF4E than for eIF4F. Here, we report the effects of PABP on the binding kinetics of cap analog binding to eIFiso4F and the temperature dependence of these reactions. These data indicate that a large part of the enhancement in binding affinity resides in the dissociation rate and that one of the significant effects of PABP is to lower the Arrehenius activation energy of the eIF4F complex. m7GTP was purchased from Sigma. Ant-m7GTP was synthesized and purified as described previously (10Ren J. Goss D.J. Nucleic Acids Res. 1996; 24: 3629-3634Crossref PubMed Scopus (31) Google Scholar) with slight modification. After completion of the synthesis reaction, there are several products in the solution, Ant-m7GTP, m7GTP, isotoic anhydride, and anthraniloyl acid. Ethanol precipitation was used to separate Ant-m7GTP and m7GTP from the fluorescent dye. For the separation of Ant-m7GTP and m7GTP, a Sephadex G-15 column (1 × 120-cm, packed in deionized water) with a flow rate of 6 ml/hr was used. Ant-m7GTP was eluted as the second peak, which was characterized by UV absorbance and thin layer chromatography. Ant-m7GTP showed two absorbance maxima at 254 and 332 nm, a shoulder at ∼ 280 nm, and a fluorescence spot on TLC plates. Ant-m7GTP was separated from Ant-m7GDP by TLC prior to use. The preparation of PABP followed the procedure of Le et al.(8Le H. Tanguay R.L. Balasta M.L. Wei C.-C. Browning K.S. Metz A.M. Goss D.J. Gallie D.R. J. Biol. Chem. 1997; 272: 16247-16255Abstract Full Text Full Text PDF PubMed Scopus (229) Google Scholar). Wheat germ eIFiso4F was obtained by mixing two subunits (P28 and P86) in 1:1 molar ratio (11Lax S.R. Fritz W. Browning K.S. Ravel J.M. Proc. Natl. Acad. Sci. U. S. A. 1985; 82: 330-332Crossref PubMed Scopus (60) Google Scholar). The pure P28 and P86 subunits were prepared as described previously (12Van Heerden A. Browning K.S. J. Biol. Chem. 1994; 269: 17454-17457Abstract Full Text PDF PubMed Google Scholar). All samples were dialyzed against Buffer A (20 mm HEPES-KOH, 100 mm potassium acetate, 1 mm CaCl2, 1 mmdithiothreitol, 1 mm EDTA, 1 mmMgCl2, pH 7.6) and passed through a 0.22 μmfilter (Millipore) before the spectroscopy measurements were performed. Protein concentrations were estimated by the method of Bradford (13Bradford M. Anal. Biochem. 1976; 72: 248-254Crossref PubMed Scopus (217544) Google Scholar) using a Bio-Rad protein assay reagent (Bio-Rad Laboratories). Absorbance measurements were obtained using a Cary-3 double-beam UV/visible spectrophotometer. Fluorescence spectra were recorded on a Spex Fluorog τ2 spectrofluorometer. All measurements were performed at 20 °C. As described elsewhere (10Ren J. Goss D.J. Nucleic Acids Res. 1996; 24: 3629-3634Crossref PubMed Scopus (31) Google Scholar, 14Darzynkiewicz E. Stepinski J. Ekiel I. Jin Y. Haber D. Sijuwade T. Tahara S.M. Nucleic Acids Res. 1988; 16: 8953-8962Crossref PubMed Scopus (71) Google Scholar, 15Stepinski J. Ekiel I. Goyer C. Sonenberg N. Termeriusz A. Jin Y. Sijuwade T. Haber D. Tahara S.M. Biochemistry. 1989; 28: 4771-4778Crossref PubMed Scopus (51) Google Scholar), P28 or eIFiso4F binding induced an increase in Ant-m7GTP fluorescence. The time course of the reaction was monitored using an Olis RSM 1000 stopped-flow system with a 1-ms dead time. Ant-m7GTP was mixed with eIFiso4E (P28), eIFiso4F, or eIFiso4F·PABP. Formation of the eIFiso4F·PABP complex was determined as described previously (6Wei C.-C. Balasta M.L. Ren J. Goss D.J. Biochemistry. 1998; 37: 1910-1916Crossref PubMed Scopus (112) Google Scholar). The excitation wavelength was at 332 nm, and emission was monitored by use of a photomultiplier after passage through a 400-nm cut-on filter. A reference photomultiplier was used to monitor fluctuations in the lamp intensity. The temperature of flow-cell and solution reservoirs was maintained using a temperature-controlled circulating water bath. After rapid mixing of the protein with the Ant-m7GTP cap analog, the data for the time course of the fluorescence intensity changes were recorded by computer data acquisition. Kinetic data were analyzed by nonlinear regression analysis using Global analysis software provided by Olis. To measure the dissociation rate constants, a complex of eIF4F·PABP·Ant-m7GTP was rapidly diluted 12-fold in a spectrofluorimeter cuvette, and the resulting decrease in fluorescence was measured. Because of the high binding affinity of the cap analog to the complex, a large dilution, which could not be accomplished by stopped-flow, was necessary. The stopped-flow data for a typical reaction curve for the binding of Ant-m7GTP to eIFiso4E and eIFiso4F are shown in Fig.1. On the ordinate is the relative voltage, which is proportional to fluorescence intensity. Time course data were fitted by nonlinear regression analysis assuming a single exponential change described by ΔFt = ΔF∞(1 − exp(−kobst)) (16Olsen K. Christensen U. Sierks M.R. Svensson B. Biochemistry. 1993; 32: 9686-9693Crossref PubMed Scopus (54) Google Scholar), where ΔFt is that fluorescence observed at any time,t, and the final fluorescence when the reaction achieves equilibrium, ΔF∞, is the difference between Ant-m7GTP fluorescence at zero time and at equilibrium, andkobs is the observed first-order rate constant. The reaction was consistent with a single exponential process. Analyses that assume two or three time-resolved exponential components did not improve the fitting results. Under the pseudo first-order conditions, where Ant-m7GTP was in excess, the observed rate constant is predicted to be a linear function of the concentration of Ant-m7GTP. However, as observed previously (1Sha M. Wang Y. Xiang T. van Heerden A. Browning K. Goss D.J. J. Biol. Chem. 1995; 270: 29904-29909Abstract Full Text Full Text PDF PubMed Scopus (38) Google Scholar), the results showed that the observed binding rates had little dependence on Ant-m7GTP concentration over a concentration range of 5–19 μm Ant-m7GTP, a 4- to 18-fold excess. The observed rate varied from 31–36 s−1. As proposed previously (1Sha M. Wang Y. Xiang T. van Heerden A. Browning K. Goss D.J. J. Biol. Chem. 1995; 270: 29904-29909Abstract Full Text Full Text PDF PubMed Scopus (38) Google Scholar, 17Garland D.L. Biochemistry. 1978; 17: 4266-4272Crossref PubMed Scopus (191) Google Scholar), the binding mechanism can be explained by a two-step process involving a fast association of eIFiso4E and Ant-m7GTP followed by a slow change of conformation from the first association complex to the stable complex. eIFiso4E+Ant­m7GTP→k1(eIFiso4E·Ant­m7GTP)*↓k2eIFiso4E·Ant­m7GTPEq. 1 The binding rates have the following relationship with the concentration of substrate: 1/kobs = 1/k2 +k1/k2[C] as described previously (16Olsen K. Christensen U. Sierks M.R. Svensson B. Biochemistry. 1993; 32: 9686-9693Crossref PubMed Scopus (54) Google Scholar), where kobs is the observed first-order rate constant, k2 is the forward rate constant for the second step, and [C] is the concentration of Ant-m7GTP. Fig. 2 is the plot of 1/kobs versus 1/[C] of eIFiso4E, which shows a linear relationship. From the intercept of 1/k2, k2 was found to be 36.9 ± 1.6 s−1. Rate constants for eIFiso4E binding to Ant-m7GTP at 4, 10, 15, 22, and 31 °C are shown in TableI. The values ofk2 for Ant-m7GTP binding to eIFiso4E at different temperatures were calculated from data sets collected at each temperature as in the example shown in Fig. 1. The derived rate constants were used to construct an Arrehenius plot (Fig.3) according to the equation lnk = −(Ea/RT) + ln A, where k is the rate constant, Ea is the activation energy, and A is the Arrehenius pre-exponential term. The activation energy was calculated from the slope of the fitted linear line of ln k versus1/T (kelvin). The activation energy for Ant-m7GTP binding to eIFiso4E, determined from the temperature dependence of the rate constants, was 63.3 ± 1.4 kJ/mol.Table IKinetic binding constants and activation energy for the interaction of eIFiso4E, eIFiso4F and eIFiso4F/PABP with Ant-m 7 GTPTemperaturek2eIFiso4EeIFiso4FeIFiso4F/PABP°Cs −1 4.06.064.4214.010.010.59.3620.015.015.917.128.522.030.637.939.031.069.810262.2Ea (kJ/mol)63.3 ± 1.481.5 ± 2.538.6 ± 1.6 Open table in a new tab Rate constants for eIFiso4F are shown in Table I. Fig. 3 also shows the Arrehenius plot for eIFiso4F. The activation energy for Ant-m7GTP and eIFiso4F binding was 81.5 ± 2.5 kJ/mol, which is significantly higher than the value obtained for eIFiso4E. PABP has been shown to affect the equilibrium binding affinity of eIFiso4F for cap analogs. To understand further the mechanism of this reaction, the effects of PABP on the kinetics of reaction were investigated. After adding PABP to eIFiso4F under conditions where a complex is formed, the activation energy decreased to 38.6 (±1.6) kJ/mol (Fig. 3). The activation energy for PABP·eIFiso4F binding to Ant-m7GTP is 2-fold lower than for the eIFiso4F and Ant-m7GTP interaction. Previous work has shown that PABP alone does not bind Ant-m7GTP6. The dissociation reaction was monitored as described above. Fig.4 shows the results of the dilution experiment. The apparent rates are more than 5-fold slower in the presence of PABP. The general mechanism of interaction of the cap with eIFiso4E and eIFiso4F is very similar. Both proteins follow a two-step binding mechanism with the first step being very fast and close to being diffusion-controlled. The rate constants for the second step were similar at about 20 °C; however, the temperature dependence was different. The similarity or rate constants for eIFiso4F and eIFiso4E is surprising. In our previous studies with a dinucleotide cap analog, we found k2 to be almost 10-fold faster for eIF4E, suggesting that the smaller protein was more able to accomplish the conformational change necessary for binding, although the equilibrium constants were similar for the two proteins. The fact that the rate constant, k2, for the two proteins are similar for the mononucleotide analog indicate that the second base must play a role in the binding. In the case of eIFiso4F, this slows down the binding, not only in comparison with eIFiso4E but also compared with the mononucleotide. The Ant-m7GTP bound eIFiso4F about 3-fold faster than m7GpppG. Our previous studies using fluorescence energy transfer have shown that PABP has a large effect on the cap equilibrium with eIFiso4F. The dissociation equilibrium constant decreased from 8.9 to 0.21 μm in the presence of PABP. PABP has been shown to interact with eIFiso4F through the P86 (eIFiso4G) subunit of eIFiso4F. Only a small effect on k2 was observed for the PABP·eIFiso4F binding of cap analog. It is unlikely there is much effect on the initial second-order binding, because that rate is close to the diffusion-controlled rate and cannot account for the large difference in equilibrium constant. The most likely explanation is that the off rate, k−2, is slower when PABP is present. To estimate the off rate, the dilution experiment described earlier was performed. This is not an ideal experiment, because concentrations of Ant-m7GTP must be such that a significant change in the amount of cap analog that is bound occurs. There must also be sufficient eIFiso4F to assure that a significant eIFiso4F·PABP complex exists. Further, because these experiments are performed in a standard 1-cm fluorescence cuvette to allow mixing, large amounts of sample are required. Fig. 4 shows the difference measured. The curve in the presence of PABP represents dissociation from both eIFiso4F and eIFiso4F·PABP. We were unable to adequately resolve two rate constants from these curves, probably because about 10–15% of the reaction occurred during the mixing time. However, a significant difference is seen in the presence of PABP indicating the dissociation rate is indeed affected. The rates are at least 5-fold slower in the presence of PABP. This difference is an underestimate of the effect of PABP on the dissociation rate. More detailed kinetic studies are in progress. The Arrehenius activation energies for the three protein systems, eIFiso4E, eIFiso4F, and eIFiso4F-PABP, were significantly different. The eIFiso4E and eIFiso4F had Arrehenius activation energies of 63.3 ± 1.4 and 81.5 ± 2.5 kJ/mol, respectively. The addition of PABP to eIFiso4F lowered the activation energy more than 2-fold. This reduced temperature dependence suggests that PABP succeeds in speeding the reaction by providing a path with a substantially lower energy barrier. The kinetic effects of PABP enhancement on cap affinity must reside primarily in the dissociation rates. A likely possibility is that PABP, which interacts with the 4G subunit, induces a conformational change that is propagated to the cap binding site. The lower activation energy suggests an intermediate that more easily achieves a stable conformation. PABP reduces the dissociation of the complex and may enhance translation by forming a more stable platform for further assembly of the initiation complex. The reduced temperature dependence of the reaction may provide a means for adapting to variations in environmental temperatures encountered by plant systems. It would not be advantageous for rapid protein synthesis to occur during environmental stress.