Variant DNA polymerases

BACKGROUND OF THE INVENTION
The present invention relates to modifications of the DNA sequencing method developed by F. Sanger (Sanger, F., Nicklen, S., Coulson, A. R. (1977) Proc. Natl. Acac. Sci. U.S.A. 74, 5463-5467) as well as to novel enzymes which can be used for DNA sequencing. The Sanger sequencing method is based on in vitro DNA synthesis reactions in the presence of a primed DNA template, 2'-deoxyribonucleoside triphosphates (dNTPs, see FIG. 1), and 2',3'-dideoxyribonucleoside triphosphates (ddNTPs, FIG. 1). The latter, when incorporated by a DNA polymerase into a polynucleotide chain, terminate further chain elongation. The DNA products are thus a series of polynucleotide chains complementary to the template and terminated with specific dideoxynucleotides. The DNA sequencing products can be separated by size and the pattern of the products gives the DNA sequence.
In principle, DNA polymerases from a variety of organisms and a variety of chain-terminating nucleotides should be useful to sequence DNA. In practice, few DNA polymerases and chain-terminating nucleotides have been found to be suitable for this purpose. As an example of a DNA sequencing polymerase, the development of bacteriophage T7 DNA polymerase, Sequenace.TM., will be reviewed (Tabor, S., and Richardson, C. C. (1990) J. Biol. Chem. 265, 8322-8328). In order to obtain an unambiguous DNA sequence it is necessary that the majority of sequencing products terminate with a dideoxynucleotide and that all the sequencing products are represented equally. Two phage T7 DNA polymerase activities degrade DNA sequencing products and, thus, these activities must be eliminated in order to prevent degradation of dideoxynucleotide-terminated sequencing products. One activity, 3'.fwdarw.5' exonuclease activity, was removed by constructing an exonuclease deficient variant of T7 DNA polymerase. T7 DNA polymerase also has pyrophosphorolytic activity which can degrade the sequencing products. Pyrophosphatase was added to degrade pyrophosphate produced in the DNA sequencing reactions; without pyrophosphate, there is no pyrophosphorolysis. A further refinement of the sequencing reactions was to use Mn.sup.2+ in place of Mg.sup.2+ which resulted in a more equal distribution of reaction products. Although this brier review of the development of T7 DNA polymerase into a sequencing polymerase is a simplification, the review illustrates the point that modification of a natural DNA polymerase as well as development of reaction conditions is required in order to obtain high quality DNA sequence information using the chain-terminating sequencing method.
Optimal DNA sequencing conditions using the chain-terminating method have not yet been achieved. Ambiguous sequencing information is still observed which necessitates determining the DNA sequence of both DNA strands. Also, the use of Mn.sup.2+ in place of Mg.sup.2+ increases the amount of DNA template required for sequencing reactions. Thus it would be advantageous to develop novel methods that would improve or complement existing sequencing procedures.
The wild type T4 DNA polymerase gene has been cloned and the protein product expressed (Lin, T.-C., Rush, J. R., Spicer, E. K., and Konigsberg, W. H. (1987) Proc. Natl. Acad. Sci. U.S.A. 84, 7000-7004; U.S. Pat. No. 4,935,361 to Lin et al.) and E. coli DNA polymerase II has been cloned and expressed (Bonner, C. A., Hays, S., McEntee, K., and Goodman, M. F. (1990) Proc. Natl. Acad. Sci. U.S.A. 87, 7663-7667). Standard oligonucleotide-directed mutagenesis techniques have been used to construct novel forms of T4 DNA polymerase and E. coli DNA polymerase II. Thus, the means exist to economically prepare large quantities of wild type and variant T4 DNA polymerase and E. coli DNA polymerase II.
Another aspect of the invention is to use genetic analysis to identify DNA polymerases with properties useful for DNA sequencing. T4 DNA polymerase is one of the most extensively genetically characterized DNA polymerases (Reha-Krantz, L. J. (1993) In Molecular Biology of Bacteriophage T4, ed. Karam J., American Association for Microbiology, in press); hence, some mutant DNA polymerases already identified may have properties useful for DNA sequencing and new mutants can be isolated directly. A method to isolate novel T4 DNA polymerases with useful DNA sequencing properties would be of additional utility.
SUMMARY OF THE INVENTION
In accordance with aspect of the invention, there are provided novel enzymes which may be used as DNA sequencing polymerases. These enzymes result from genetic mutations of family B DNA polymerases. These mutations eliminate the 3'.fwdarw.5' exonuclease activity of these novel family B DNA polymerases.
In accordance with another aspect of the invention, there are provided methods that enable phage T4 DNA polymerase and E. coli DNA polymerase II to be used as DNA sequencing polymerases. DNA polymerase modifications that convert phage T4 DNA polymerase and E. coli DNA polymerase II into DNA sequencing polymerases can also be used to similarly modify DNA polymerases having protein sequence homology with these two polymerases. DNA polymerases with protein sequence similarities to T4 DNA polymerase and E. coli DNA polymerase II include, but are not limited to, a group of DNA polymerases that are called Family B DNA polymerases (Braithwaite, D. K. and Ito, J. (1993) Nucl. Acids Res. 21, 787-802). Of particular relevance are the DNA polymerases from phages T2 and T6 which have extensive protein sequence homology to T4 DNA polymerase. Another extension of methods described here is that DNA polymerases with functional similarities to T4 DNA polymerase and E. coli DNA polymerase II may also be used to produce DNA sequence information with the chain-terminating nucleotides and methods disclosed hereinafter.
In accordance with another aspect of this invention there is provided a method to identify DNA polymerase modifications, having one or more specific amino acid substitutions in the polymerase protein sequence, that improve a given DNA polymerase in terms of DNA sequencing applications.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 depicts the structure of standard nucleotides and nucleotide analogs useful in the practice of the invention.
FIGS. 2A-C depict DNA sequencing gels which resulted from the use of variant E. coli DNA polymerase II and T4 DNA polymerase.
FIG. 3 depicts a DNA sequencing gel in which dATP is used at very low concentrations compared to the other standard nucleotides.
FIG. 4 depicts primer extension past a template abasic site (X) by wild-type and mutant T4 DNA polymerases.

DETAILED DESCRIPTION OF THE INVENTION
An aspect of the invention, namely to identify modified DNA polymerases with new properties that improve the ability of the modified DNA polymerases to carry out DNA sequencing reactions, is achieved by the design of a new genetic selection strategy that identifies modified DNA polymerases with superior DNA replication activities. The new genetic selection strategy has been designed around the T4 DNA polymerase.
T4 DNA polymerase (SEQ ID NOS: 3 and 4) and E. coli DNA polymerase II (SEQ ID NOS: 5 and 6), which have heretofore been unable to be used as sequencing polymerases, can be used as DNA sequencing polymerases in Sanger-type reactions if non-standard or novel combinations of chain-terminating nucleotides are used. Further to this discovery is the finding that inactivation of 3'.fwdarw.5' exonuclease activity in T4 DNA polymerase and E. coli DNA polymerase II improves the quality of the DNA sequence information obtained. In a further aspect, additional polymerase modifications have been discovered, which when combined with other modifications that reduce 3'.fwdarw.5' exonuclease activity, have the potential to produce a multiply modified DNA polymerase with advantageous DNA sequencing properties. Due to extensive sequence homology with T4 DNA polymerase, DNA polymerases such as phages T2 (SEQ ID NOS: 1 and 2) and T6 DNA polymerases are particularly suitable in the application of the methods of the invention.
T4 DNA polymerase and E. coli DNA polymerase II can be used as effective DNA sequencing polymerases if the arabinonucleotides (FIG. 1), araUTP and araCTP, are used in place of the standard chain-terminating nucleotides ddTTP and ddCTP. The standard purine dideoxynucleotides (FIG. 1), ddATP and ddGTP, are effective chain-terminating nucleotides for T4 DNA polymerase and E. coli DNA polymerase II. DNA sequencing reactions for T4 DNA polymerase and E. coli DNA polymerase II differ from standard DNA sequencing reactions in that a novel combination of chain-terminating nucleotides is used. Although in principle any chain-terminating nucleotide may be used, DNA polymerases differ markedly in their ability to incorporate these nucleotides into the DNA chain. For T4 DNA polymerase and E. coli DNA polymerase II, the low incorporation of ddTTP and ddCTP by these enzymes have prevented the use of these standard chain-terminating nucleotides in sequencing protocols. The discovery that alternative chain-terminating arabinonucleotides, araCTP and araUTP, can be incorporated relatively efficiently by T4 DNA polymerase and E. coli DNA polymerase II enables these DNA polymerases to be used as sequencing polymerases. The DNA sequencing method that uses reactions with the novel combinations of chain-terminating nucleotides--araCTP, araUTP, ddATP and ddGTP, is described, hereinbelow, in Method I.
A further discovery is that inactivation or significant reduction of the 3'.fwdarw.5' exonuclease activity of T4 DNA polymerase and E. coli DNA polymerase II enhances the quality of DNA sequence information obtained using the Method I sequencing reactions. T4 DNA polymerase 3'.fwdarw.5' exonuclease activity can be significantly reduced by an amino acid substitution including, but not limited to, one or more of the following amino acid substitutions in the enzyme: D112A+E114A, D219A and D324A. In the above nomenclature which is used herein throughout, the single letter code for amino acids is used. The numbers flanked by the single letter codes for amino acids are the codon numbers. For example, D112A+E114A indicates an alanine (A) substitution for aspartate (D) at codon position 112. D112A+E114A indicates two amino acid substitutions in the modified DNA polymerase. To achieve these variants the following mutations were employed: for D112A the A nucleotide at position 335 is replaced with a C nucleotide thereby effecting a change of the D amino acid to an A amino acid, as is known to one of ordinary skill in the art other nucleotide changes are capable of effecting the same change; for E114A the A nucleotide at position 341 is replaced with a C nucleotide, as is known other nucleotide changes can effect the same amino acid change; for D219A the A nucleotide at position 656 is replaced with a C nucleotide, respectively, as is known other nucleotide changes can effect the same amino acid change; and for D324A the A nucleotide at position 971 is replaced with a C nucleotide, as is known other nucleotide changes can effect the same amino acid change. E. coli DNA polymerase II 3'.fwdarw.5' exonuclease activity can be significantly reduced by an amino acid substitution including, but not limited to, the following amino acid substitutions: D156A+E158A. To achieve these variants the following mutations were employed: for D156A the A nucleotide at position 467 is replaced with a C nucleotide, as is known other nucleotide changes can effect the same amino acid change; for E158A the A nucleotide at position 473 is replaced with a C nucleotide, as is known other nucleotide changes can effect the same amino acid change. Construction of 3'.fwdarw.5' exonuclease deficient variants of T4 DNA polymerase and E. coli DNA polymerase II is achieved by standard oligonucleotide mutagenesis procedures (for example, Kunkle, T. A., Roberts, J. D. and Zakour, R. A. (1987) Method. Enz. 154, 367-382).
Another aspect of the invention may be achieved by using chain-terminating nucleotides that are not used in standard DNA sequencing reactions. T4 DNA polymerase and E. coli DNA polymerase II may also be used as effective DNA sequencing polymerases if 3'amino-2',3'-dideoxyribonucleotides (3'-NH.sub.2 dNTPs) (FIG. 1) are used in place of the standard ddNTPs. This sequencing method is described herein below in Method II. Unmodified (wild type) T4 DNA polymerase and 3'.fwdarw.5' exonuclease deficient variants can be used in Method II reactions; the 3'.fwdarw.5' exonuclease deficient variant of E. coli DNA polymerase II has also been successfully used in Method II reactions.
The 3'.fwdarw.5' exonuclease deficient form of T4 DNA polymerase can also be used to produce DNA sequence information without nucleotide analogs if the concentration of one of the four standard dNTPs is very low. For example, if the concentrations of dGTP, dCTP and dTTP are at 100 .mu.M and the concentration of dATP is at 0.1 .mu.M to 1 .mu.M then sequencing products are observed that terminate one position before dATP is required for incorporation. With parallel reactions, each with one dNTP present at low concentration and the other three dNTPs present at high concentrations, the DNA sequence can be determined. This sequencing method is referred to hereinafter as Method III.
The third objective, namely to identify variant or modified DNA polymerases with new properties that enable the polymerases to have enhanced sequencing properties, has been achieved by designing a new strategy to select for novel DNA polymerases. The new strategy, a type of genetic selection, was developed for phage T4. The basic strategy begins with a phage T4 strain that has one or more mutations in the DNA polymerase gene which result in a variant (mutant) DNA polymerase which is partially defective in some aspect of DNA replication. Several types of DNA polymerase modifications can reduce the ability of DNA polymerase to replicate DNA efficiently. For example, alterations in the ability of the DNA polymerase to bind DNA template or dNTPs or in the ability of the DNA polymerase to translocate along the DNA template will reduce DNA replication efficiency. For phage T4, DNA polymerase mutants with reduced DNA replication activity can be readily identified. Phage T4 strains with mutant DNA polymerases that are partially defective in DNA replication cannot synthesize DNA if the bacterial host used in the infection contains the optA1 mutation. In other words, the E. coli optA1 host restricts growth of T4 strains with mutant DNA polymerases defective in DNA replication activity. The basis of the restriction observed for the E. coli optA1 strain is that increased amounts of an enzyme that degrades dGTP is produced (Wurgler, S. S., and Richardson, C. C. (1990) Proc. Natl. Acad. Sci. U.S.A. 87, 2740-2744). Thus, phage T4 strains with variant DNA polymerases with reduced DNA replication activity cannot replicate DNA and produce phage progeny if the nucleotide pools, especially dGTP, are reduced.
In terms of development of a genetic selection strategy, conditions have been established which can be used to identify DNA replication defective DNA polymerases as well as to restrict production of progeny from phages with such defective DNA polymerases, namely the restricted production of phage progeny in infections of the E. coli optA1 bacterial host. These conditions, described hereinbelow, enable the selection of further modified (mutated) DNA polymerases with superior DNA replication ability. If the variant DNA polymerases with reduced DNA replication activity are further modified, for example by one or more additional amino acid substitutions, it may be that additional mutations/amino acid substitutions correct or compensate for the initial defect in DNA replication activity. Such further modified DNA polymerases will now be able to replicate DNA in the E coli optA1 host and phage progeny will be produced. Thus, detection of phage progeny on the E. coli optA1 host in infections with phage formerly restricted from producing progeny on this host allows for the selection of multiply mutant DNA polymerases that have the starting mutation (amino acid substitutions that decrease DNA replication activity) plus one or more new mutations that encode additional amino acid substitutions that correct or compensate for the starting DNA replication defect. The new correcting or compensating mutations (also called suppressor mutations in genetic terminology) can be identified by sequencing the phage DNA polymerase gene using standard procedures (McPheeters, D. S., Christensen, A., Young, E. T., Stormo, G., and Gold, L. (1986) Nucleic Acid Res. 14, 5813-5826; Reha-Krantz, L. J. (1988) J. Mol. Biol. 202, 711-724). The new mutations can be introduced into the phage T4 DNA polymerase gene or into T4 DNA polymerase expression vectors for further study. In contrast to the starting phage T4 DNA polymerases with reduced DNA replication ability, the new variant DNA polymerases have superior DNA replication ability because these variant DNA polymerases were selected on the basis of their ability to overcome, compensate or correct defects in variant DNA polymerase with reduced DNA replication activity. The genetic strategy to identify variant DNA polymerases with superior DNA replication abilities is highly sensitive as a single phage with the above described properties can be selected from a population of 10.sup.8 to 10.sup.9 phage.
Further to the invention, variant DNA polymerases with superior DNA replication activity have properties advantageous for DNA sequencing polymerase, such as enhanced primer extension which produces a more uniform distribution of sequencing products and enhanced DNA replication in template regions that may block or hinder replication by unmodified DNA polymerases. T4 DNA polymerase variants with superior DNA replication ability are predicted to improve the quality of DNA sequence information produced by Methods I, II, and III.
The genetic selection strategy described here for the detection of variant DNA polymerases with superior DNA replication ability can be applied to the DNA polymerases of other organisms it such defective DNA polymerases can be identified and if variants with correcting or compensating mutations can be selected.
DNA Sequencing Method I.
T4 DNA polymerase with significantly reduced 3'.fwdarw.5' exonuclease activity, such as variant forms with either D112A+E114A, D219A, or D324A amino acid substitutions, and E. coli DNA polymerase II with significantly reduced 3'.fwdarw.5' exonuclease activity, such as the variant form with D156A+E158A amino acid substitutions, can be used as DNA sequencing polymerases with the following set of chain-terminating nucleotides: ddATP, ddGTP, araCTP, and araUTP (FIG. 1).
FIG. 2 shows photographs of three DNA sequencing gels. DNA sequencing patterns obtained with Method I are in panels A and B, lanes 1-4, and panel C. Panel A shows DNA sequencing reactions with the exonuclease deficient variant of E. coli DNA polymerase II. The reaction with ddGTP is in lane 1, the reaction with ddATP is in lane 2, the reaction with araCTP is in lane 3, and the reaction with araUTP is in lane 4. Panel B shows DNA sequencing reactions with the exonuclease deficient form of bacteriophage T4 DNA polymerase. Again, lane 1 has reactions with ddGTP, lane 2 has ddATP, lane 3 has araCTP, and lane 4 has araUTP. The reactions in panels A and B have Mg.sup.2+ as the divalent metal cation. Sequencing patters are also obtained with Mn.sup.2+ in place of Mg.sup.2+. Method I reactions with Mn.sup.2+ with the exonuclease deficient form of E. coli DNA polymerase II are shown on the left side of panel C, lanes 1-4; reactions with the exonuclease deficient form of T4 DNA polymerase are shown on the right side of panel C, lanes 1-4. Panel C, lanes 1-4 contain reactions with ddGTP (lane 1), ddATP (lane 2), araCTP (lane 3), and araUTP (lane 4).
DNA Sequencing Method II.
Wild type (unmodified) and 3'.fwdarw.5' exonuclease deficient forms of T4 DNA polymerase and the 3'.fwdarw.5' exonuclease deficient form of E. coli DNA polymerase II can be used as DNA sequencing polymerases with 3' amino-2', 3'-dideoxyribonucleotides (FIG. 1) as chain terminating nucleotides. Method II reactions for the exonuclease deficient form of E. coli DNA polymerase II are shown in FIG. 2, panel A, lanes 5-7. Lane five shows the reaction with 3'amino-2',3'-dideoxyGTP; lane 6 shows the reaction with 3'amino-2',3'-dideoxyATP; lane 7 shows the reaction with 3'amino-2',3-dideoxyTTP. Method II reactions for the exonuclease deficient form of T4 DNA polymerase are shown in panel B, lanes 5-7. Lane 5, 6 and 7 show reactions with 3'amino-2'3'dideoxyGTP, -ATP and -TTP, respectively.
The data demonstrate that the exonuclease deficient forms of E. coli DNA polymerase II and bacteriophage T4 DNA polymerases can produce DNA sequence information using a combination of the following chain-terminating nucleotides: ddGTP or 3'amino-2',3'-dideoxyGTP; ddATP or 3'amino-2',3'dideoxyATP; araUTP or 3'amino-2',3'dideoxy-TTP; and araCTP. In view of the good sequence patterns obtained with 3'amino-2'3'dideoxy-GTP, -ATP and -TTP, it is likely that 3'amino-2',3'-dideoxy-CTP will also be an effective chain-terminating nucleotide. No attempt was made to optimize conditions for Methods I or II in order to achieve equal band intensities or to increase the length of readable sequence for the reactions shown in FIG. 2. Nevertheless, the sequencing methods can provide sequence information for at least 300 bases. The exonuclease deficient form of T4 DNA polymerase is not required for sequencing reactions with the 3'amino-2', 3'-dideoxyribonucleoside triphosphates.
Sample Experimental Conditions for Methods I and II (FIG. 2).
Labeling reaction.
5 .mu.l exonuclease deficient DNA polymerase; 300-400 units/ml for T4 DNA polymerase or for E. coli DNA polymerase II. One unit T4 DNA polymerase catalyzes 10 nmol of dTMP incorporation into DNA in 30 min at 30.degree. C. One unit of E. coli DNA polymerase II catalyzes the incorporation of 1 pmol of dTMP into DNA in 1 min at 37.degree. C. Although the reaction is typically conducted at 37.degree. C., the reaction may be conducted in a temperature range from about 35.degree. C. to about 42.degree. C.
15 .mu.l primer-M13 DNA complex, 15 nM
15 .mu.l labeling reaction solution: 2 .mu.M dGTP, dCTP, dTTP; 1 .mu.M �.alpha..sup.32 P!dATP; 50 mM Tris-HCl (pH 8.5); 5 mM MgCl.sub.2 or 6 mM MnCl.sub.2 for E. coli DNA polymerase II; 5 mM MgCl.sub.2 or 0.5 mM MnCl.sub.2 for T4 DNA polymerase; 5 mM dithiothreitol; 50 .mu.g/ml bovine serum albumin.
The reaction mixtures were incubated 5 min at 37.degree. C.
The primer may also be labeled at the 5'-end, or by including a labeled nucleotide in the extension reaction and by other standard methods.
Extension Reaction.
4 .mu.l labeling reaction mixture (from above)
4 .mu.l termination solution: 50 .mu.M dGTP, dATP, dCTP and dTTP; and one of the termination analogs listed below:
Method I: ddGTP, 1.6 mM; ddATP, 0.7 mM; araCTP, 0.5 mM; araUTP, 0.5 mM.
Method II: 3'-amino-2',3'-dideoxyGTP, 0.5 mM; 3'-amino-2',3-dideoxyATP, 0.5 mM; 3'-amino-2',3'-dideoxyTTP, 0.5 mM.
Reactions were incubated at 5 min at 37.degree. C. Reactions were stopped by adding formamide/EDTA.
DNA Sequencing Method III (FIG. 3).
Exonuclease deficient T4 DNA polymerase can produce DNA sequence information in reactions where one dNTP is at a low concentration (for example, 0.1 .mu.M to 1 .mu.M) and the other three dNTPs are at high concentrations (100 .mu.M) (FIG. 3). DNA sequencing patterns are produced as with sequencing reactions with nucleotide analogs except that sequencing products produced by this method terminate one position before the dNTP at low concentrations is required.
Sample Experimental Conditions:
25 mM Hepes (pH 7.5)
60 mM NaOAc
1 mM dithiothreitol
100 .mu.M dGTP, dCTP and dTTP
0.1 .mu.M dATP (1 .mu.M dATP for longer DNA products)
0.2 mg/ml bovine serum albumin 7.5 nM 5'�.sup.32 P!labeled primer-template (expressed as the concentration of 3'-primer termini)
30 nM exonuclease deficient T4 DNA polymerase
6 mM Mg(OAc).sub.2
The reaction shown in FIG. 3 contained 0.1 .mu.M dATP and was incubated for 1 min at 30.degree. C. Conditions have not been optimized to obtain high amounts of sequence information; however, reactions in which the low concentration dNTP is at 1 .mu.l yield sequence information greater than 100 bases.
Isolation of Novel T4 DNA Polymerases with Properties Advantageous for DNA Sequencing.
The first step in this aspect of the invention is to identify T4 strains with variant (mutant) DNA polymerases defective in some aspect of DNA replication. T4 strains with mutant DNA polymerase that have the amino acid substitutions listed below were chosen, but the genetic selection strategy is not limited to these mutants as any mutant DNA polymerase with defective DNA replication ability can be used. Variant (mutant) T4 DNA polymerases that are partially defective in some aspect of DNA replication cannot replicate DNA in the E. coli optA1 host.
T4 strains with mutant DNA polymerases with amino acid substitutions W213S, I417V, A737V or A777V cannot replicate DNA in the E. coli optA1 host. To achieve these variants the following mutations were employed: for W213S the G nucleotide at position 638 is replaced with a C nucleotide; for I417V the A nucleotide at position 1249 is replaced with a G nucleotide; for A737V the C nucleotide at position 2210 is replaced with a T nucleotide; and for A777V the C nucleotide at position 2330 is replaced with a T nucleotide. As is known other nucleotide replacements can cause the same amino acid changes.
The second step is to select T4 strains that can replicate DNA in the E. coli optA1 host even though the DNA polymerase still retains the amino acid substitution that alone reduces DNA replication ability and prevents replication of DNA in E. coli ontA1 host. T4 strains that have acquired a second DNA polymerase mutation (or multiple mutations), either by spontaneous mutation or by mutagenesis treatment, that encodes a new amino acid substitution that can correct or compensate the DNA replication defect produced by the first amino acid substitution, will be able to replicate DNA in the E. coli optA1 host and produce phage progeny. DNA polymerases thus identified have at least two amino acid substitutions: the starting amino acid substitution and one or more new amino acid substitutions that restore DNA replication activity. This genetic selection strategy is of high sensitivity. A phage with a mutant DNA polymerase containing the starting amino acid substitution and the amino acid substitution(s) that restores DNA replication activity can be selected from a population of 10.sup.8 to 10.sup.9 phage.
The third step is to identify the DNA replication restoring mutation(s). This step utilizes standard sequencing procedures to find the new mutation(s) in the T4 DNA polymerase gene. Once the new mutation(s) has been identified, the mutation can be introduced into phage or into T4 DNA polymerase expression vectors using standard procedures. Unlike the starting, DNA replication defective DNA polymerase, the DNA polymerases with the correcting or compensating amino acid substitutions have superior DNA replication activity. A sample of the amino acid substitutions discovered using the genetic selection strategy described above include but are not limited to: I50L, G82D, G255S and E743K. To achieve these variants the following mutations were employed: for I50L the A nucleotide at position 148 is replaced with a C nucleotide; for G82D the G nucleotide at position 245 is replaced with an A nucleotide; for G255S the G nucleotide at position 763 is replaced with an A nucleotide; and for E743K the G nucleotide at position 2227 is replaced with an A nucleotide. As is known other nucleotide replacements can effect the same amino acid changes.
Variant (mutant, modified) T4 DNA polymerases with amino acid substitutions that confer enhanced DNA replication activity have new properties advantageous for DNA sequencing. One frequent DNA sequencing problem is that DNA polymerases used in sequencing reactions pause or disassociate at some template sites. As a consequence of this premature stop in chain elongation, sequencing products are produced that are not terminated by a chain-terminating nucleotide. Another problem is that DNA polymerase incorporation of nucleotides and chain-terminating nucleotides is affected by the template sequence which may lead to an unequal distribution of sequencing products. Novel DNA polymerases with enhanced DNA replication activity may surmount these problems. The G82D-T4 DNA polymerase (also known as T4 mel 62 DNA polymerase) has been tested in primer extension assays and this novel DNA polymerase has been found to extend primers that are problematic for the wild type T4 DNA polymerase. An example of G82D-T4 DNA polymerase synthesis is given in FIG. 4.
FIG. 4 depicts the use of three T4 polymerases to copy a DNA template lesion (an abasic lesion--a base is missing on the template strand, indicated by X). The wild-type T4 polymerase has difficulty incorporating a nucleotide opposite X, as shown by the very light bands. A 3'-exonuclease deficient T4 polymerase mutant, EXO.sup.- 17, is able to incorporate nucleotides opposite X (note the intense band at X) and continue synthesis beyond the lesion. The T4 mel 62 polymerase is a mutant enzyme (it conveys a mutator phenotype in vivo) that has apparent normal (wild-type) levels of 3'-exonuclease and polymerase activities. It nevertheless is also able to incorporate nucleotides opposite X and to continue synthesis beyond X. What is most interesting is that the absence of "pausing" bands beyond X suggests that the mel 62 DNA polymerase remains bound to the primer template DNA more tightly than either EXO.sup.- 17 or the wild-type polymerases. Thus, it is possible that this enzyme may be able to overcome template and substrate obstacles to synthesize long stretches of DNA.
It is contemplated that one or more amino acid substitutions that confer superior DNA replication activity will be combined with one or more amino acid substitutions that significantly reduce 3'.fwdarw.5' exonuclease activity to create a multiply modified novel T4 DNA polymerase with several properties that are advantageous for DNA sequencing polymerases.
It is known that polymerases, such as bacteriophage T7 DNA polymerase, may be used in conjunction with their accessory proteins thereby increasing the processivity of the polymerase by decreasing the rate of disassociation of the polymerase from the DNA strand to be sequenced.
In the case of the T4 polymerase, its accessory proteins, include but are not limited to, the following T4 gene products: gene product 32, 41, 45 and the 44/62 complex. In the case of E. coli DNA polymerase II, the accessory proteins are the following: .beta. protein; the .gamma. protein complex wherein the .gamma. complex is composed of .gamma., .delta., .delta.', .chi., .psi.; and SSB (single stranded binding protein) (note that .beta. protein and .gamma. complex are E. coli pol III accessory proteins). Use of these accessory proteins enhances the efficiency of the polymerases in sequencing DNA.
While there have been shown and described the fundamental novel features of the invention, it will be understood that various omissions, substitutions and changes in the form and details illustrated may be made by those skilled in the art without departing from the spirit of the invention. It is the invention, therefore, to be limited only as indicated by the scope of the following claims.
__________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 6- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 2694 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 1..2694- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:- ATG AAA GAA TTT TAT ATC TCT ATC GAA ACA GT - #C GGA AAT AAT ATT 45Met Lys Glu Phe Tyr Ile Ser Ile Glu Thr Va - #l Gly Asn Asn Ile# 15- ATT GAA CGT TAT ATT GAT GAA AAC GGA AAG GA - #A CGT ACT CGT GAA 90Ile Glu Arg Tyr Ile Asp Glu Asn Gly Lys Gl - #u Arg Thr Arg Glu# 30- GTA GAA TAT CTT CCG ACT ATG TTT AGG CAT TG - #T AAG GAA GAG TCA 135Val Glu Tyr Leu Pro Thr Met Phe Arg His Cy - #s Lys Glu Glu Ser# 45- AAA TAC AAA GAC ATC TAT GGT AAA AAC TGT GC - #T CCT CAA AAA TTT 180Lys Tyr Lys Asp Ile Tyr Gly Lys Asn Cys Al - #a Pro Gln Lys Phe# 60- CCA TCA ATG AAA GAT GCT CGA GAT TGG ATG AA - #G CGA ATG GAA GAC 225Pro Ser Met Lys Asp Ala Arg Asp Trp Met Ly - #s Arg Met Glu Asp# 75- ATC GGT CTC GAA GCT CTC GGT ATG AAC GAT TT - #T AAA CTC GCT TAT 270Ile Gly Leu Glu Ala Leu Gly Met Asn Asp Ph - #e Lys Leu Ala Tyr# 90- ATC AGT GAT ACG TAT GGT TCA GAA ATT GTT TA - #T GAC CGA AAA TTT 315Ile Ser Asp Thr Tyr Gly Ser Glu Ile Val Ty - #r Asp Arg Lys Phe# 105- GTT CGT GTA GCT AAC TGT GAC ATT GAG GTT AC - #T GGT GAT AAA TTT 360Val Arg Val Ala Asn Cys Asp Ile Glu Val Th - #r Gly Asp Lys Phe# 120- CCT GAC CCA ATG AAA GCA GAA TAT GAA ATT GA - #T GCT ATC ACT CAT 405Pro Asp Pro Met Lys Ala Glu Tyr Glu Ile As - #p Ala Ile Thr His# 135- TAT GAT TCA ATT GAC GAC CGT TTT TAT GTT TT - #C GAC CTT TTG AAT 450Tyr Asp Ser Ile Asp Asp Arg Phe Tyr Val Ph - #e Asp Leu Leu Asn# 150- TCA ATG TAC GGT TCA GTA TCA AAA TGG GAT GC - #A AAG TTA GCT GCT 495Ser Met Tyr Gly Ser Val Ser Lys Trp Asp Al - #a Lys Leu Ala Ala# 165- AAG CTT GAC TGT GAA GGT GGT GAT GAA GTT CC - #T CAA GAA ATT CTT 540Lys Leu Asp Cys Glu Gly Gly Asp Glu Val Pr - #o Gln Glu Ile Leu# 180- GAC CGA GTA ATT TAT ATG CCA TTT GAT AAT GA - #G CGT GAT ATG CTC 585Asp Arg Val Ile Tyr Met Pro Phe Asp Asn Gl - #u Arg Asp Met Leu# 195- ATG GAA TAT ATT AAT CTC TGG GAA CAG AAA CG - #A CCT GCT ATT TTT 630Met Glu Tyr Ile Asn Leu Trp Glu Gln Lys Ar - #g Pro Ala Ile Phe# 210- ACT GGT TGG AAT ATT GAG GGG TTT GAC GTT CC - #G TAT ATC ATG AAT 675Thr Gly Trp Asn Ile Glu Gly Phe Asp Val Pr - #o Tyr Ile Met Asn# 225- CGC GTT AAA ATG ATT CTG GGT GAA CGC AGT AT - #G AAA CGT TTC TCT 720Arg Val Lys Met Ile Leu Gly Glu Arg Ser Me - #t Lys Arg Phe Ser# 240- CCA ATC GGT CGG GTA AAA TCT AAA CTA ATT CA - #A AAT ATG TAC GGT 765Pro Ile Gly Arg Val Lys Ser Lys Leu Ile Gl - #n Asn Met Tyr Gly# 255- AGC AAA GAA ATT TAT TCT ATT GAT GGC GTA TC - #T ATT CTT GAT TAT 810Ser Lys Glu Ile Tyr Ser Ile Asp Gly Val Se - #r Ile Leu Asp Tyr# 270- TTA GAT TTG TAC AAG AAA TTC GCT TTT ACT AA - #T TTG CCG TCA TTC 855Leu Asp Leu Tyr Lys Lys Phe Ala Phe Thr As - #n Leu Pro Ser Phe# 285- TCT TTG GAA TCA GTT GCT CAA CAT GAA ACC AA - #A AAA GGT AAA TTA 900Ser Leu Glu Ser Val Ala Gln His Glu Thr Ly - #s Lys Gly Lys Leu# 300- CCA TAC GAC GGT CCT ATT AAT AAA CTT CGT GA - #G ACT AAT CAT CAA 945Pro Tyr Asp Gly Pro Ile Asn Lys Leu Arg Gl - #u Thr Asn His Gln# 315- CGA TAC ATT AGT TAT AAC ATC ATT GAC GTA GA - #A TCA GTT CAA GCA 990Arg Tyr Ile Ser Tyr Asn Ile Ile Asp Val Gl - #u Ser Val Gln Ala# 330- ATT GAT AAA ATT CGT GGG TTT ATC GAT CTA GT - #T TTA AGT ATG TCT 1035Ile Asp Lys Ile Arg Gly Phe Ile Asp Leu Va - #l Leu Ser Met Ser# 345- TAT TAT GCT AAA ATG CCT TTT TCT GGT GTA AT - #G AGT CCT ATT AAA 1080Tyr Tyr Ala Lys Met Pro Phe Ser Gly Val Me - #t Ser Pro Ile Lys# 360- ACT TGG GAT GCT ATT ATT TTT AAC TCA TTG AA - #A GGT GAA CAC AAG 1125Thr Trp Asp Ala Ile Ile Phe Asn Ser Leu Ly - #s Gly Glu His Lys# 375- GTT ATT CCT CAA CAA GGT TCG CAC GTT AAA CA - #G AGT TTT CCG GGT 1170Val Ile Pro Gln Gln Gly Ser His Val Lys Gl - #n Ser Phe Pro Gly# 390- GCA TTT GTA TTT GAA CCT AAA CCA ATT GCT CG - #T CGA TAC ATT ATG 1215Ala Phe Val Phe Glu Pro Lys Pro Ile Ala Ar - #g Arg Tyr Ile Met# 405- AGT TTT GAC TTG ACG TCT CTG TAT CCG AGC AT - #T ATT CGC CAG GTT 1260Ser Phe Asp Leu Thr Ser Leu Tyr Pro Ser Il - #e Ile Arg Gln Val# 420- AAC ATT AGT CCT GAA ACT ATT CGT GGT CAG TT - #T AAA GTT CAT CCA 1305Asn Ile Ser Pro Glu Thr Ile Arg Gly Gln Ph - #e Lys Val His Pro# 435- ATT CAT GAA TAT ATC GCA GGA ACA GCT CCT AA - #A CCA AGT GAT GAA 1350Ile His Glu Tyr Ile Ala Gly Thr Ala Pro Ly - #s Pro Ser Asp Glu# 450- TAT TCT TGT TCT CCG AAT GGA TGG ATG TAT GA - #T AAG CAT CAA GAA 1395Tyr Ser Cys Ser Pro Asn Gly Trp Met Tyr As - #p Lys His Gln Glu# 465- GGT ATC ATT CCA AAG GAA ATC GCT AAA GTA TT - #T TTC CAG CGT AAA 1440Gly Ile Ile Pro Lys Glu Ile Ala Lys Val Ph - #e Phe Gln Arg Lys# 480- GAT TGG AAA AAG AAA ATG TTC GCT GAA GAA AT - #G AAT GCC GAA GCT 1485Asp Trp Lys Lys Lys Met Phe Ala Glu Glu Me - #t Asn Ala Glu Ala# 495- ATT AAA AAG ATT ATT ATG AAA GGC GCA GGG TC - #T TGT TCA ACT AAA 1530Ile Lys Lys Ile Ile Met Lys Gly Ala Gly Se - #r Cys Ser Thr Lys# 510- CCA GAA GTT GAA CGA TAT GTT AAG TTC ACT GA - #T GAT TTC TTA AAT 1575Pro Glu Val Glu Arg Tyr Val Lys Phe Thr As - #p Asp Phe Leu Asn# 525- GAA CTA TCG AAT TAT ACT GAA TCT GTT CTT AA - #T AGT CTG ATT GAA 1620Glu Leu Ser Asn Tyr Thr Glu Ser Val Leu As - #n Ser Leu Ile Glu# 540- GAA TGT GAA AAA GCA GCT ACA CTT GCT AAT AC - #A AAT CAG CTG AAC 1665Glu Cys Glu Lys Ala Ala Thr Leu Ala Asn Th - #r Asn Gln Leu Asn# 555- CGT AAA ATT CTT ATT AAC AGT CTT TAT GGT GC - #T CTT GGT AAT ATT 1710Arg Lys Ile Leu Ile Asn Ser Leu Tyr Gly Al - #a Leu Gly Asn Ile# 570- CAT TTC CGT TAC TAT GAT TTA CGA AAT GCT AC - #T GCT ATC ACA ATT 1755His Phe Arg Tyr Tyr Asp Leu Arg Asn Ala Th - #r Ala Ile Thr Ile# 585- TTT GGT CAA GTT GGT ATT CAG TGG ATT GCT CG - #T AAA ATT AAT GAA 1800Phe Gly Gln Val Gly Ile Gln Trp Ile Ala Ar - #g Lys Ile Asn Glu# 600- TAT CTG AAT AAA GTA TGC GGA ACT AAT GAT GA - #A GAT TTC ATC GCA 1845Tyr Leu Asn Lys Val Cys Gly Thr Asn Asp Gl - #u Asp Phe Ile Ala# 615- GCA GGT GAT ACT GAT TCG GTA TAT GTT TGT GT - #A GAT AAA GTT ATT 1890Ala Gly Asp Thr Asp Ser Val Tyr Val Cys Va - #l Asp Lys Val Ile# 630- GAA AAA GTT GGT CTT GAC CGA TTC AAA GAG CA - #G AAC GAT TTG GTT 1935Glu Lys Val Gly Leu Asp Arg Phe Lys Glu Gl - #n Asn Asp Leu Val# 645- GAA TTC ATG AAT CAG TTT GGT AAG AAA AAG AT - #G GAA CCT ATG ATT 1980Glu Phe Met Asn Gln Phe Gly Lys Lys Lys Me - #t Glu Pro Met Ile# 660- GAT GTT GCA TAT CGT GAG TTA TGT GAT TAT AT - #G AAT AAC CGC GAG 2025Asp Val Ala Tyr Arg Glu Leu Cys Asp Tyr Me - #t Asn Asn Arg Glu# 675- CAT CTG ATG CAT ATG GAC CGT GAA GCT ATT TC - #T TGC CCT CCG CTT 2070His Leu Met His Met Asp Arg Glu Ala Ile Se - #r Cys Pro Pro Leu# 690- GGT TCA AAG GGT GTT GGT GGA TTT TGG AAA GC - #G AAA AAA CGT TAT 2115Gly Ser Lys Gly Val Gly Gly Phe Trp Lys Al - #a Lys Lys Arg Tyr# 705- GCT CTG AAC GTT TAT GAT ATG GAA GAT AAG CG - #A TTT GCT GAA CCG 2160Ala Leu Asn Val Tyr Asp Met Glu Asp Lys Ar - #g Phe Ala Glu Pro# 720- CAT CTA AAA ATC ATG GGT ATG GAA ACT CAG CA - #G AGT TCA ACA CCA 2205His Leu Lys Ile Met Gly Met Glu Thr Gln Gl - #n Ser Ser Thr Pro# 735- AAA GCA GTG CAA GAA GCA CTC GAA GAA AGT AT - #T CGT CGT ATT CTT 2250Lys Ala Val Gln Glu Ala Leu Glu Glu Ser Il - #e Arg Arg Ile Leu# 750- CAG GAA GGC GAA GAG TCT GTC CAA GAA TAT TA - #C AAG AAC TTC GAG 2295Gln Glu Gly Glu Glu Ser Val Gln Glu Tyr Ty - #r Lys Asn Phe Glu# 765- AAA GAA TAT CGT CAA CTT GAC TAT AAA GTT AT - #T GCT GAA GTA AAA 2340Lys Glu Tyr Arg Gln Leu Asp Tyr Lys Val Il - #e Ala Glu Val Lys# 780- ACT GCG AAC GAT ATA GCG AAA TAT GAT GAT AA - #A GGT TGG CCA GGA 2385Thr Ala Asn Asp Ile Ala Lys Tyr Asp Asp Ly - #s Gly Trp Pro Gly# 795- TTT AAA TGT CCG TTC CAT ATT CGT GGT GTG CT - #A ACT TAT CGT CGA 2430Phe Lys Cys Pro Phe His Ile Arg Gly Val Le - #u Thr Tyr Arg Arg# 810- GCT GTT AGT GGT CTG GGT GTA GCT CCA ATT TT - #G GAT GGA AAT AAA 2475Ala Val Ser Gly Leu Gly Val Ala Pro Ile Le - #u Asp Gly Asn Lys# 825- GTA ATG GTT CTT CCA TTA CGT GAA GGA AAT CC - #G TTT GGT GAT AAG 2520Val Met Val Leu Pro Leu Arg Glu Gly Asn Pr - #o Phe Gly Asp Lys# 840- TGC ATT GCT TGG CCA TCG GGT ACA GAA CTT CC - #A AAA GAA ATT CGT 2565Cys Ile Ala Trp Pro Ser Gly Thr Glu Leu Pr - #o Lys Glu Ile Arg# 8550- TCT GAT GTA CTA TCT TGG ATT GAC TAC TCA AC - #T TTG TTC CAA AAA 2610Ser Asp Val Leu Ser Trp Ile Asp Tyr Ser Th - #r Leu Phe Gln Lys# 870- TCG TTT GTT AAA CCG CTT GCG GGT ATG TGT GA - #A TCG GCA GGT ATG 2655Ser Phe Val Lys Pro Leu Ala Gly Met Cys Gl - #u Ser Ala Gly Met# 885- GAC TAT GAG GAA AAA GCT TCG TTA GAC TTC CT - #G TTT GGC 2694Asp Tyr Glu Glu Lys Ala Ser Leu Asp Phe Le - #u Phe Gly# 898 895- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 898 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:- Met Lys Glu Phe Tyr Ile Ser Ile Glu Thr Va - #l Gly Asn Asn Ile# 15- Ile Glu Arg Tyr Ile Asp Glu Asn Gly Lys Gl - #u Arg Thr Arg Glu# 30- Val Glu Tyr Leu Pro Thr Met Phe Arg His Cy - #s Lys Glu Glu Ser# 45- Lys Tyr Lys Asp Ile Tyr Gly Lys Asn Cys Al - #a Pro Gln Lys Phe# 60- Pro Ser Met Lys Asp Ala Arg Asp Trp Met Ly - #s Arg Met Glu Asp# 75- Ile Gly Leu Glu Ala Leu Gly Met Asn Asp Ph - #e Lys Leu Ala Tyr# 90- Ile Ser Asp Thr Tyr Gly Ser Glu Ile Val Ty - #r Asp Arg Lys Phe# 105- Val Arg Val Ala Asn Cys Asp Ile Glu Val Th - #r Gly Asp Lys Phe# 120- Pro Asp Pro Met Lys Ala Glu Tyr Glu Ile As - #p Ala Ile Thr His# 135- Tyr Asp Ser Ile Asp Asp Arg Phe Tyr Val Ph - #e Asp Leu Leu Asn# 150- Ser Met Tyr Gly Ser Val Ser Lys Trp Asp Al - #a Lys Leu Ala Ala# 165- Lys Leu Asp Cys Glu Gly Gly Asp Glu Val Pr - #o Gln Glu Ile Leu# 180- Asp Arg Val Ile Tyr Met Pro Phe Asp Asn Gl - #u Arg Asp Met Leu# 195- Met Glu Tyr Ile Asn Leu Trp Glu Gln Lys Ar - #g Pro Ala Ile Phe# 210- Thr Gly Trp Asn Ile Glu Gly Phe Asp Val Pr - #o Tyr Ile Met Asn# 225- Arg Val Lys Met Ile Leu Gly Glu Arg Ser Me - #t Lys Arg Phe Ser# 240- Pro Ile Gly Arg Val Lys Ser Lys Leu Ile Gl - #n Asn Met Tyr Gly# 255- Ser Lys Glu Ile Tyr Ser Ile Asp Gly Val Se - #r Ile Leu Asp Tyr# 270- Leu Asp Leu Tyr Lys Lys Phe Ala Phe Thr As - #n Leu Pro Ser Phe# 285- Ser Leu Glu Ser Val Ala Gln His Glu Thr Ly - #s Lys Gly Lys Leu# 300- Pro Tyr Asp Gly Pro Ile Asn Lys Leu Arg Gl - #u Thr Asn His Gln# 315- Arg Tyr Ile Ser Tyr Asn Ile Ile Asp Val Gl - #u Ser Val Gln Ala# 330- Ile Asp Lys Ile Arg Gly Phe Ile Asp Leu Va - #l Leu Ser Met Ser# 345- Tyr Tyr Ala Lys Met Pro Phe Ser Gly Val Me - #t Ser Pro Ile Lys# 360- Thr Trp Asp Ala Ile Ile Phe Asn Ser Leu Ly - #s Gly Glu His Lys# 375- Val Ile Pro Gln Gln Gly Ser His Val Lys Gl - #n Ser Phe Pro Gly# 390- Ala Phe Val Phe Glu Pro Lys Pro Ile Ala Ar - #g Arg Tyr Ile Met# 405- Ser Phe Asp Leu Thr Ser Leu Tyr Pro Ser Il - #e Ile Arg Gln Val# 420- Asn Ile Ser Pro Glu Thr Ile Arg Gly Gln Ph - #e Lys Val His Pro# 435- Ile His Glu Tyr Ile Ala Gly Thr Ala Pro Ly - #s Pro Ser Asp Glu# 450- Tyr Ser Cys Ser Pro Asn Gly Trp Met Tyr As - #p Lys His Gln Glu# 465- Gly Ile Ile Pro Lys Glu Ile Ala Lys Val Ph - #e Phe Gln Arg Lys# 480- Asp Trp Lys Lys Lys Met Phe Ala Glu Glu Me - #t Asn Ala Glu Ala# 495- Ile Lys Lys Ile Ile Met Lys Gly Ala Gly Se - #r Cys Ser Thr Lys# 510- Pro Glu Val Glu Arg Tyr Val Lys Phe Thr As - #p Asp Phe Leu Asn# 525- Glu Leu Ser Asn Tyr Thr Glu Ser Val Leu As - #n Ser Leu Ile Glu# 540- Glu Cys Glu Lys Ala Ala Thr Leu Ala Asn Th - #r Asn Gln Leu Asn# 555- Arg Lys Ile Leu Ile Asn Ser Leu Tyr Gly Al - #a Leu Gly Asn Ile# 570- His Phe Arg Tyr Tyr Asp Leu Arg Asn Ala Th - #r Ala Ile Thr Ile# 585- Phe Gly Gln Val Gly Ile Gln Trp Ile Ala Ar - #g Lys Ile Asn Glu# 600- Tyr Leu Asn Lys Val Cys Gly Thr Asn Asp Gl - #u Asp Phe Ile Ala# 615- Ala Gly Asp Thr Asp Ser Val Tyr Val Cys Va - #l Asp Lys Val Ile# 630- Glu Lys Val Gly Leu Asp Arg Phe Lys Glu Gl - #n Asn Asp Leu Val# 645- Glu Phe Met Asn Gln Phe Gly Lys Lys Lys Me - #t Glu Pro Met Ile# 660- Asp Val Ala Tyr Arg Glu Leu Cys Asp Tyr Me - #t Asn Asn Arg Glu# 675- His Leu Met His Met Asp Arg Glu Ala Ile Se - #r Cys Pro Pro Leu# 690- Gly Ser Lys Gly Val Gly Gly Phe Trp Lys Al - #a Lys Lys Arg Tyr# 705- Ala Leu Asn Val Tyr Asp Met Glu Asp Lys Ar - #g Phe Ala Glu Pro# 720- His Leu Lys Ile Met Gly Met Glu Thr Gln Gl - #n Ser Ser Thr Pro# 735- Lys Ala Val Gln Glu Ala Leu Glu Glu Ser Il - #e Arg Arg Ile Leu# 750- Gln Glu Gly Glu Glu Ser Val Gln Glu Tyr Ty - #r Lys Asn Phe Glu# 765- Lys Glu Tyr Arg Gln Leu Asp Tyr Lys Val Il - #e Ala Glu Val Lys# 780- Thr Ala Asn Asp Ile Ala Lys Tyr Asp Asp Ly - #s Gly Trp Pro Gly# 795- Phe Lys Cys Pro Phe His Ile Arg Gly Val Le - #u Thr Tyr Arg Arg# 810- Ala Val Ser Gly Leu Gly Val Ala Pro Ile Le - #u Asp Gly Asn Lys# 825- Val Met Val Leu Pro Leu Arg Glu Gly Asn Pr - #o Phe Gly Asp Lys# 840- Cys Ile Ala Trp Pro Ser Gly Thr Glu Leu Pr - #o Lys Glu Ile Arg# 855- Ser Asp Val Leu Ser Trp Ile Asp Tyr Ser Th - #r Leu Phe Gln Lys# 870- Ser Phe Val Lys Pro Leu Ala Gly Met Cys Gl - #u Ser Ala Gly Met# 885- Asp Tyr Glu Glu Lys Ala Ser Leu Asp Phe Le - #u Phe Gly# 898 895- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 2694 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 1..2694- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:- ATG AAA GAA TTT TAT ATC TCT ATT GAA ACA GT - #C GGA AAT AAC ATT 45Met Lys Glu Phe Tyr Ile Ser Ile Glu Thr Va - #l Gly Asn Asn Ile# 15- GTT GAA CGT TAT ATT GAT GAA AAT GGA AAG GA - #A CGT ACC CGT GAA 90Val Glu Arg Tyr Ile Asp Glu Asn Gly Lys Gl - #u Arg Thr Arg Glu# 30- GTA GAA TAT CTT CCA ACT ATG TTT AGG CAT TG - #T AAG GAA GAG TCA 135Val Glu Tyr Leu Pro Thr Met Phe Arg His Cy - #s Lys Glu Glu Ser# 45- AAA TAC AAA GAC ATC TAT GGT AAA AAC TGC GC - #T CCT CAA AAA TTT 180Lys Tyr Lys Asp Ile Tyr Gly Lys Asn Cys Al - #a Pro Gln Lys Phe# 60- CCA TCA ATG AAA GAT GCT CGA GAT TGG ATG AA - #G CGA ATG GAA GAC 225Pro Ser Met Lys Asp Ala Arg Asp Trp Met Ly - #s Arg Met Glu Asp# 75- ATC GGT CTC GAA GCT CTC GGT ATG AAC GAT TT - #T AAA CTC GCT TAT 270Ile Gly Leu Glu Ala Leu Gly Met Asn Asp Ph - #e Lys Leu Ala Tyr# 90- ATA AGT GAT ACA TAT GGT TCA GAA ATT GTT TA - #T GAC CGA AAA TTT 315Ile Ser Asp Thr Tyr Gly Ser Glu Ile Val Ty - #r Asp Arg Lys Phe# 105- GTT CGT GTA GCT AAC TGT GAC ATT GAG GTT AC - #T GGT GAT AAA TTT 360Val Arg Val Ala Asn Cys Asp Ile Glu Val Th - #r Gly Asp Lys Phe# 120- CCT GAC CCA ATG AAA GCA GAA TAT GAA ATT GA - #T GCT ATC ACT CAT 405Pro Asp Pro Met Lys Ala Glu Tyr Glu Ile As - #p Ala Ile Thr His# 135- TAC GAT TCA ATT GAC GAT CGT TTT TAT GTT TT - #C GAC CTT TTG AAT 450Tyr Asp Ser Ile Asp Asp Arg Phe Tyr Val Ph - #e Asp Leu Leu Asn# 150- TCA ATG TAC GGT TCA GTA TCA AAA TGG GAT GC - #A AAG TTA GCT GCT 495Ser Met Tyr Gly Ser Val Ser Lys Trp Asp Al - #a Lys Leu Ala Ala# 165- AAG CTT GAC TGT GAA GGT GGT GAT GAA GTT CC - #T CAA GAA ATT CTT 540Lys Leu Asp Cys Glu Gly Gly Asp Glu Val Pr - #o Gln Glu Ile Leu# 180- GAC CGA GTA ATT TAT ATG CCA TTC GAT AAT GA - #G CGT GAT ATG CTC 585Asp Arg Val Ile Tyr Met Pro Phe Asp Asn Gl - #u Arg Asp Met Leu# 195- ATG GAA TAT ATC AAT CTT TGG GAA CAG AAA CG - #A CCT GCT ATT TTT 630Met Glu Tyr Ile Asn Leu Trp Glu Gln Lys Ar - #g Pro Ala Ile Phe# 210- ACT GGT TGG AAT ATT GAG GGG TTT GAC GTT CC - #G TAT ATC ATG AAT 675Thr Gly Trp Asn Ile Glu Gly Phe Asp Val Pr - #o Tyr Ile Met Asn# 225- CGT GTT AAA ATG ATT CTG GGT GAA CGT AGT AT - #G AAA CGT TTC TCT 720Arg Val Lys Met Ile Leu Gly Glu Arg Ser Me - #t Lys Arg Phe Ser# 240- CCA ATC GGT CGG GTA AAA TCT AAA CTA ATT CA - #A AAT ATG TAC GGT 765Pro Ile Gly Arg Val Lys Ser Lys Leu Ile Gl - #n Asn Met Tyr Gly# 255- AGC AAA GAA ATT TAT TCT ATT GAT GGC GTA TC - #T ATT CTT GAT TAT 810Ser Lys Glu Ile Tyr Ser Ile Asp Gly Val Se - #r Ile Leu Asp Tyr# 270- TTA GAT TTG TAC AAG AAA TTC GCT TTT ACT AA - #T TTG CCG TCA TTC 855Leu Asp Leu Tyr Lys Lys Phe Ala Phe Thr As - #n Leu Pro Ser Phe# 285- TCT TTG GAA TCA GTT GCT CAA CAT GAA ACC AA - #A AAA GGT AAA TTA 900Ser Leu Glu Ser Val Ala Gln His Glu Thr Ly - #s Lys Gly Lys Leu# 300- CCA TAC GAC GGT CCT ATT AAT AAA CTT CGT GA - #G ACT AAT CAT CAA 945Pro Tyr Asp Gly Pro Ile Asn Lys Leu Arg Gl - #u Thr Asn His Gln# 315- CGA TAC ATT AGT TAT AAC ATC ATT GAC GTA GA - #A TCA GTT CAA GCA 990Arg Tyr Ile Ser Tyr Asn Ile Ile Asp Val Gl - #u Ser Val Gln Ala# 330- ATC GAT AAA ATT CGT GGG TTT ATC GAT CTA GT - #T TTA AGT ATG TCT 1035Ile Asp Lys Ile Arg Gly Phe Ile Asp Leu Va - #l Leu Ser Met Ser# 345- TAT TAC GCT AAA ATG CCT TTT TCT GGT GTA AT - #G AGT CCT ATT AAA 1080Tyr Tyr Ala Lys Met Pro Phe Ser Gly Val Me - #t Ser Pro Ile Lys# 360- ACT TGG GAT GCT ATT ATT TTT AAC TCA TTG AA - #A GGT GAA CAT AAG 1125Thr Trp Asp Ala Ile Ile Phe Asn Ser Leu Ly - #s Gly Glu His Lys# 375- GTT ATT CCT CAA CAA GGT TCG CAC GTT AAA CA - #G AGT TTT CCG GGT 1170Val Ile Pro Gln Gln Gly Ser His Val Lys Gl - #n Ser Phe Pro Gly# 390- GCA TTT GTG TTT GAA CCT AAA CCA ATT GCA CG - #T CGA TAC ATT ATG 1215Ala Phe Val Phe Glu Pro Lys Pro Ile Ala Ar - #g Arg Tyr Ile Met# 405- AGT TTT GAC TTG ACG TCT CTG TAT CCG AGC AT - #T ATT CGC CAG GTT 1260Ser Phe Asp Leu Thr Ser Leu Tyr Pro Ser Il - #e Ile Arg Gln Val# 420- AAC ATT AGT CCT GAA ACT ATT CGT GGT CAG TT - #T AAA GTT CAT CCA 1305Asn Ile Ser Pro Glu Thr Ile Arg Gly Gln Ph - #e Lys Val His Pro# 435- ATT CAT GAA TAT ATC GCA GGA ACA GCT CCT AA - #A CCG AGT GAT GAA 1350Ile His Glu Tyr Ile Ala Gly Thr Ala Pro Ly - #s Pro Ser Asp Glu# 450- TAT TCT TGT TCT CCG AAT GGA TGG ATG TAT GA - #T AAA CAT CAA GAA 1395Tyr Ser Cys Ser Pro Asn Gly Trp Met Tyr As - #p Lys His Gln Glu# 465- GGT ATC ATT CCA AAG GAA ATC GCT AAA GTA TT - #T TTC CAG CGT AAA 1440Gly Ile Ile Pro Lys Glu Ile Ala Lys Val Ph - #e Phe Gln Arg Lys# 480- GAC TGG AAA AAG AAA ATG TTC GCT GAA GAA AT - #G AAT GCC GAA GCT 1485Asp Trp Lys Lys Lys Met Phe Ala Glu Glu Me - #t Asn Ala Glu Ala# 495- ATT AAA AAG ATT ATT ATG AAA GGC GCA GGG TC - #T TGT TCA ACT AAA 1530Ile Lys Lys Ile Ile Met Lys Gly Ala Gly Se - #r Cys Ser Thr Lys# 510- CCA GAA GTT GAA CGA TAT GTT AAG TTC AGT GA - #T GAT TTC TTA AAT 1575Pro Glu Val Glu Arg Tyr Val Lys Phe Ser As - #p Asp Phe Leu Asn# 525- GAA CTA TCG AAT TAC ACC GAA TCT GTT CTC AA - #T AGT CTG ATT GAA 1620Glu Leu Ser Asn Tyr Thr Glu Ser Val Leu As - #n Ser Leu Ile Glu# 540- GAA TGT GAA AAA GCA GCT ACA CTT GCT AAT AC - #A AAT CAG CTG AAC 1665Glu Cys Glu Lys Ala Ala Thr Leu Ala Asn Th - #r Asn Gln Leu Asn# 555- CGT AAA ATT CTC ATT AAC AGT CTT TAT GGT GC - #T CTT GGT AAT ATT 1710Arg Lys Ile Leu Ile Asn Ser Leu Tyr Gly Al - #a Leu Gly Asn Ile# 570- CAT TTC CGT TAC TAT GAT TTG CGA AAT GCT AC - #T GCT ATC ACA ATT 1755His Phe Arg Tyr Tyr Asp Leu Arg Asn Ala Th - #r Ala Ile Thr Ile# 585- TTC GGC CAA GTC GGT ATT CAG TGG ATT GCT CG - #T AAA ATT AAT GAA 1800Phe Gly Gln Val Gly Ile Gln Trp Ile Ala Ar - #g Lys Ile Asn Glu# 600- TAT CTG AAT AAA GTA TGC GGA ACT AAT GAT GA - #A GAT TTC ATT GCA 1845Tyr Leu Asn Lys Val Cys Gly Thr Asn Asp Gl - #u Asp Phe Ile Ala# 615- GCA GGT GAT ACT GAT TCG GTA TAT GTT TGC GT - #A GAT AAA GTT ATT 1890Ala Gly Asp Thr Asp Ser Val Tyr Val Cys Va - #l Asp Lys Val Ile# 630- GAA AAA GTT GGT CTT GAC CGA TTC AAA GAG CA - #G AAC GAT TTG GTT 1935Glu Lys Val Gly Leu Asp Arg Phe Lys Glu Gl - #n Asn Asp Leu Val# 645- GAA TTC ATG AAT CAG TTC GGT AAG AAA AAG AT - #G GAA CCT ATG ATT 1980Glu Phe Met Asn Gln Phe Gly Lys Lys Lys Me - #t Glu Pro Met Ile# 660- GAT GTT GCA TAT CGT GAG TTA TGT GAT TAT AT - #G AAT AAC CGC GAG 2025Asp Val Ala Tyr Arg Glu Leu Cys Asp Tyr Me - #t Asn Asn Arg Glu# 675- CAT CTG ATG CAT ATG GAC CGT GAA GCT ATT TC - #T TGC CCT CCG CTT 2070His Leu Met His Met Asp Arg Glu Ala Ile Se - #r Cys Pro Pro Leu# 690- GGT TCA AAG GGC GTT GGT GGA TTT TGG AAA GC - #G AAA AAG CGT TAT 2115Gly Ser Lys Gly Val Gly Gly Phe Trp Lys Al - #a Lys Lys Arg Tyr# 705- GCT CTG AAC GTT TAT GAT ATG GAA GAT AAG CG - #A TTT GCT GAA CCG 2160Ala Leu Asn Val Tyr Asp Met Glu Asp Lys Ar - #g Phe Ala Glu Pro# 720- CAT CTA AAA ATC ATG GGT ATG GAA ACT CAG CA - #G AGT TCA ACA CCA 2205His Leu Lys Ile Met Gly Met Glu Thr Gln Gl - #n Ser Ser Thr Pro# 735- AAA GCA GTG CAA GAA GCT CTC GAA GAA AGT AT - #T CGT CGT ATT CTT 2250Lys Ala Val Gln Glu Ala Leu Glu Glu Ser Il - #e Arg Arg Ile Leu# 750- CAG GAA GGT GAA GAG TCT GTC CAA GAA TAC TA - #C AAG AAC TTC GAG 2295Gln Glu Gly Glu Glu Ser Val Gln Glu Tyr Ty - #r Lys Asn Phe Glu# 765- AAA GAA TAT CGT CAA CTT GAC TAT AAA GTT AT - #T GCT GAA GTA AAA 2340Lys Glu Tyr Arg Gln Leu Asp Tyr Lys Val Il - #e Ala Glu Val Lys# 780- ACT GCG AAC GAT ATA GCG AAA TAT GAT GAT AA - #A GGT TGG CCA GGA 2385Thr Ala Asn Asp Ile Ala Lys Tyr Asp Asp Ly - #s Gly Trp Pro Gly# 795- TTT AAA TGC CCG TTC CAT ATT CGT GGT GTG CT - #A ACT TAT CGT CGA 2430Phe Lys Cys Pro Phe His Ile Arg Gly Val Le - #u Thr Tyr Arg Arg# 810- GCT GTT AGC GGT TTA GGT GTA GCT CCA ATT TT - #G GAT GGA AAT AAA 2475Ala Val Ser Gly Leu Gly Val Ala Pro Ile Le - #u Asp Gly Asn Lys# 825- GTA ATG GTT CTT CCA TTA CGT GAA GGA AAT CC - #A TTT GGT GAC AAG 2520Val Met Val Leu Pro Leu Arg Glu Gly Asn Pr - #o Phe Gly Asp Lys# 840- TGC ATT GCT TGG CCA TCG GGT ACA GAA CTT CC - #A AAA GAA ATT CGT 2565Cys Ile Ala Trp Pro Ser Gly Thr Glu Leu Pr - #o Lys Glu Ile Arg# 8550- TCT GAT GTG CTA TCT TGG ATT GAC CAC TCA AC - #T TTG TTC CAA AAA 2610Ser Asp Val Leu Ser Trp Ile Asp His Ser Th - #r Leu Phe Gln Lys# 870- TCG TTT GTT AAA CCG CTT GCG GGT ATG TGT GA - #A TCG GCT GGC ATG 2655Ser Phe Val Lys Pro Leu Ala Gly Met Cys Gl - #u Ser Ala Gly Met# 885- GAC TAT GAA GAA AAA GCT TCG TTA GAC TTC CT - #G TTT GGC 2694Asp Tyr Glu Glu Lys Ala Ser Leu Asp Phe Le - #u Phe Gly# 898 895- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 898 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:- Met Lys Glu Phe Tyr Ile Ser Ile Glu Thr Va - #l Gly Asn Asn Ile# 15- Val Glu Arg Tyr Ile Asp Glu Asn Gly Lys Gl - #u Arg Thr Arg Glu# 30- Val Glu Tyr Leu Pro Thr Met Phe Arg His Cy - #s Lys Glu Glu Ser# 45- Lys Tyr Lys Asp Ile Tyr Gly Lys Asn Cys Al - #a Pro Gln Lys Phe# 60- Pro Ser Met Lys Asp Ala Arg Asp Trp Met Ly - #s Arg Met Glu Asp# 75- Ile Gly Leu Glu Ala Leu Gly Met Asn Asp Ph - #e Lys Leu Ala Tyr# 90- Ile Ser Asp Thr Tyr Gly Ser Glu Ile Val Ty - #r Asp Arg Lys Phe# 105- Val Arg Val Ala Asn Cys Asp Ile Glu Val Th - #r Gly Asp Lys Phe# 120- Pro Asp Pro Met Lys Ala Glu Tyr Glu Ile As - #p Ala Ile Thr His# 135- Tyr Asp Ser Ile Asp Asp Arg Phe Tyr Val Ph - #e Asp Leu Leu Asn# 150- Ser Met Tyr Gly Ser Val Ser Lys Trp Asp Al - #a Lys Leu Ala Ala# 165- Lys Leu Asp Cys Glu Gly Gly Asp Glu Val Pr - #o Gln Glu Ile Leu# 180- Asp Arg Val Ile Tyr Met Pro Phe Asp Asn Gl - #u Arg Asp Met Leu# 195- Met Glu Tyr Ile Asn Leu Trp Glu Gln Lys Ar - #g Pro Ala Ile Phe# 210- Thr Gly Trp Asn Ile Glu Gly Phe Asp Val Pr - #o Tyr Ile Met Asn# 225- Arg Val Lys Met Ile Leu Gly Glu Arg Ser Me - #t Lys Arg Phe Ser# 240- Pro Ile Gly Arg Val Lys Ser Lys Leu Ile Gl - #n Asn Met Tyr Gly# 255- Ser Lys Glu Ile Tyr Ser Ile Asp Gly Val Se - #r Ile Leu Asp Tyr# 270- Leu Asp Leu Tyr Lys Lys Phe Ala Phe Thr As - #n Leu Pro Ser Phe# 285- Ser Leu Glu Ser Val Ala Gln His Glu Thr Ly - #s Lys Gly Lys Leu# 300- Pro Tyr Asp Gly Pro Ile Asn Lys Leu Arg Gl - #u Thr Asn His Gln# 315- Arg Tyr Ile Ser Tyr Asn Ile Ile Asp Val Gl - #u Ser Val Gln Ala# 330- Ile Asp Lys Ile Arg Gly Phe Ile Asp Leu Va - #l Leu Ser Met Ser# 345- Tyr Tyr Ala Lys Met Pro Phe Ser Gly Val Me - #t Ser Pro Ile Lys# 360- Thr Trp Asp Ala Ile Ile Phe Asn Ser Leu Ly - #s Gly Glu His Lys# 375- Val Ile Pro Gln Gln Gly Ser His Val Lys Gl - #n Ser Phe Pro Gly# 390- Ala Phe Val Phe Glu Pro Lys Pro Ile Ala Ar - #g Arg Tyr Ile Met# 405- Ser Phe Asp Leu Thr Ser Leu Tyr Pro Ser Il - #e Ile Arg Gln Val# 420- Asn Ile Ser Pro Glu Thr Ile Arg Gly Gln Ph - #e Lys Val His Pro# 435- Ile His Glu Tyr Ile Ala Gly Thr Ala Pro Ly - #s Pro Ser Asp Glu# 450- Tyr Ser Cys Ser Pro Asn Gly Trp Met Tyr As - #p Lys His Gln Glu# 465- Gly Ile Ile Pro Lys Glu Ile Ala Lys Val Ph - #e Phe Gln Arg Lys# 480- Asp Trp Lys Lys Lys Met Phe Ala Glu Glu Me - #t Asn Ala Glu Ala# 495- Ile Lys Lys Ile Ile Met Lys Gly Ala Gly Se - #r Cys Ser Thr Lys# 510- Pro Glu Val Glu Arg Tyr Val Lys Phe Ser As - #p Asp Phe Leu Asn# 525- Glu Leu Ser Asn Tyr Thr Glu Ser Val Leu As - #n Ser Leu Ile Glu# 540- Glu Cys Glu Lys Ala Ala Thr Leu Ala Asn Th - #r Asn Gln Leu Asn# 555- Arg Lys Ile Leu Ile Asn Ser Leu Tyr Gly Al - #a Leu Gly Asn Ile# 570- His Phe Arg Tyr Tyr Asp Leu Arg Asn Ala Th - #r Ala Ile Thr Ile# 585- Phe Gly Gln Val Gly Ile Gln Trp Ile Ala Ar - #g Lys Ile Asn Glu# 600- Tyr Leu Asn Lys Val Cys Gly Thr Asn Asp Gl - #u Asp Phe Ile Ala# 615- Ala Gly Asp Thr Asp Ser Val Tyr Val Cys Va - #l Asp Lys Val Ile# 630- Glu Lys Val Gly Leu Asp Arg Phe Lys Glu Gl - #n Asn Asp Leu Val# 645- Glu Phe Met Asn Gln Phe Gly Lys Lys Lys Me - #t Glu Pro Met Ile# 660- Asp Val Ala Tyr Arg Glu Leu Cys Asp Tyr Me - #t Asn Asn Arg Glu# 675- His Leu Met His Met Asp Arg Glu Ala Ile Se - #r Cys Pro Pro Leu# 690- Gly Ser Lys Gly Val Gly Gly Phe Trp Lys Al - #a Lys Lys Arg Tyr# 705- Ala Leu Asn Val Tyr Asp Met Glu Asp Lys Ar - #g Phe Ala Glu Pro# 720- His Leu Lys Ile Met Gly Met Glu Thr Gln Gl - #n Ser Ser Thr Pro# 735- Lys Ala Val Gln Glu Ala Leu Glu Glu Ser Il - #e Arg Arg Ile Leu# 750- Gln Glu Gly Glu Glu Ser Val Gln Glu Tyr Ty - #r Lys Asn Phe Glu# 765- Lys Glu Tyr Arg Gln Leu Asp Tyr Lys Val Il - #e Ala Glu Val Lys# 780- Thr Ala Asn Asp Ile Ala Lys Tyr Asp Asp Ly - #s Gly Trp Pro Gly# 795- Phe Lys Cys Pro Phe His Ile Arg Gly Val Le - #u Thr Tyr Arg Arg# 810- Ala Val Ser Gly Leu Gly Val Ala Pro Ile Le - #u Asp Gly Asn Lys# 825- Val Met Val Leu Pro Leu Arg Glu Gly Asn Pr - #o Phe Gly Asp Lys# 840- Cys Ile Ala Trp Pro Ser Gly Thr Glu Leu Pr - #o Lys Glu Ile Arg# 855- Ser Asp Val Leu Ser Trp Ile Asp His Ser Th - #r Leu Phe Gln Lys# 870- Ser Phe Val Lys Pro Leu Ala Gly Met Cys Gl - #u Ser Ala Gly Met# 885- Asp Tyr Glu Glu Lys Ala Ser Leu Asp Phe Le - #u Phe Gly# 898 895- (2) INFORMATION FOR SEQ ID NO:5:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 2459 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 108..2456- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:# 50CG CGAAGGCATA TTACGGGCAG TAATGACTGT ATAAAACCAC# 100AA ACGAAACCAG GCTATACTCA AGCCTGGTTT TTTGATGGAT#CGA 137GCA GGT TTT ATC TTA ACC#Ile Leu Thr ArgGln Ala Gly Phe# 10- CAC TGG CGG GAC ACC CCG CAA GGG ACA GAA GT - #C TCC TTC TGG CTG 182His Trp Arg Asp Thr Pro Gln Gly Thr Glu Va - #l Ser Phe Trp Leu# 25- GCG ACG GAC AAC GGG CCG TTG CAG GTT ACG CT - #T GCA CCG CAA GAG 227Ala Thr Asp Asn Gly Pro Leu Gln Val Thr Le - #u Ala Pro Gln Glu# 40- TCC GTG GCG TTT ATT CCC GCC GAT CAG GTT CC - #C CGC GCT CAG CAT 272Ser Val Ala Phe Ile Pro Ala Asp Gln Val Pr - #o Arg Ala Gln His# 55- ATT TTG CAG GGT GAA CAA GGC TTT CGC CTG AC - #A CCG CTG GCG TTA 317Ile Leu Gln Gly Glu Gln Gly Phe Arg Leu Th - #r Pro Leu Ala Leu# 70- AAG GAT TTT CAC CGC CAG CCG GTG TAT GGC CT - #T TAC TGT CGC GCC 362Lys Asp Phe His Arg Gln Pro Val Tyr Gly Le - #u Tyr Cys Arg Ala# 85- CAT CGC CAA TTG ATG AAT TAC GAA AAG CGC CT - #G CGT GAA GGT GGC 407His Arg Gln Leu Met Asn Tyr Glu Lys Arg Le - #u Arg Glu Gly Gly# 100- GTT ACC GTC TAC GAG GCC GAT GTG CGT CCG CC - #A GAA CGC TAT CTG 452Val Thr Val Tyr Glu Ala Asp Val Arg Pro Pr - #o Glu Arg Tyr Leu# 115- ATG GAG CGG TTT ATC ACC TCA CCG GTG TGG GT - #C GAG GGT GAT ATG 497Met Glu Arg Phe Ile Thr Ser Pro Val Trp Va - #l Glu Gly Asp Met# 130- CAC AAT GGC ACT ATC GTT AAT GCC CGT CTG AA - #A CCG CAT CCC GAC 542His Asn Gly Thr Ile Val Asn Ala Arg Leu Ly - #s Pro His Pro Asp# 145- TAT CGT CCG CCG CTC AAG TGG GTT TCT ATA GA - #T ATT GAA ACC ACC 587Tyr Arg Pro Pro Leu Lys Trp Val Ser Ile As - #p Ile Glu Thr Thr# 160- CGC CAC GGT GAG CTG TAC TGC ATC GGC CTG GA - #A GGC TGC GGG CAG 632Arg His Gly Glu Leu Tyr Cys Ile Gly Leu Gl - #u Gly Cys Gly Gln# 175- CGC ATC GTT TAT ATG CTG GGG CCG GAG AAT GG - #C GAC GCC TCC TCG 677Arg Ile Val Tyr Met Leu Gly Pro Glu Asn Gl - #y Asp Ala Ser Ser# 190- CTT GAT TTC GAA CTG GAA TAC GTC GCC AGC CG - #C CCG CAG TTG CTG 722Leu Asp Phe Glu Leu Glu Tyr Val Ala Ser Ar - #g Pro Gln Leu Leu# 205- GAA AAA CTC AAC GCC TGG TTT GCC AAC TAC GA - #T CCT GAT GTG ATC 767Glu Lys Leu Asn Ala Trp Phe Ala Asn Tyr As - #p Pro Asp Val Ile# 220- ATC GGT TGG AAC GTG GTG CAG TTC GAT CTG CG - #A ATG CTG CAA AAA 812Ile Gly Trp Asn Val Val Gln Phe Asp Leu Ar - #g Met Leu Gln Lys# 235- CAT GCC GAG CGT TAC CGT CTT CCG CTG CGT CT - #T GGG CGC GAT AAT 857His Ala Glu Arg Tyr Arg Leu Pro Leu Arg Le - #u Gly Arg Asp Asn# 250- AGC GAG CTG GAG TGG CGC GAC GAC GGC TTT AA - #A AAC GGC GTC TTT 902Ser Glu Leu Glu Trp Arg Asp Asp Gly Phe Ly - #s Asn Gly Val Phe# 265- TTT GCC CAG GCT AAA GGT GGG CTA ATT ATC GA - #C GGT ATC GAG GCG 947Phe Ala Gln Ala Lys Gly Gly Leu Ile Ile As - #p Gly Ile Glu Ala# 280- CTG AAA TCC GCG TTC TGG AAT TTC TCT TCA TT - #C TCG CTG GAA ACT 992Leu Lys Ser Ala Phe Trp Asn Phe Ser Ser Ph - #e Ser Leu Glu Thr# 295- GTC GCT CAG GAG CTA TTA GGC GAA GGA AAA TC - #T ATC GAT AAC CCG 1037Val Ala Gln Glu Leu Leu Gly Glu Gly Lys Se - #r Ile Asp Asn Pro# 310- TGG GAT CGA ATG GAC GAA ATT GAC CGC CGT TT - #C GCC GAA GAT AAA 1082Trp Asp Arg Met Asp Glu Ile Asp Arg Arg Ph - #e Ala Glu Asp Lys# 325- CCT GCG CTG GCA ACT TAT AAC CTG AAA GAT TG - #C GAG CTG GTG ACG 1127Pro Ala Leu Ala Thr Tyr Asn Leu Lys Asp Cy - #s Glu Leu Val Thr# 340- CAG ATC TTC CAC AAA ACT GAA ATC ATG CCA TT - #T TTA CTC GAA CGG 1172Gln Ile Phe His Lys Thr Glu Ile Met Pro Ph - #e Leu Leu Glu Arg# 355- GCA ACG GTG AAC GGC CTG CCG GTG GAC CGA CA - #C GGC GGT TCG GTG 1217Ala Thr Val Asn Gly Leu Pro Val Asp Arg Hi - #s Gly Gly Ser Val# 370- GCG GCA TTT GGT CAT CTC TAT TTT CCG CGA AT - #G CAT CGC GCT GGT 1262Ala Ala Phe Gly His Leu Tyr Phe Pro Arg Me - #t His Arg Ala Gly# 385- TAT GTC GCG CCT AAT CTC GGC GAA GTG CCG CC - #G CAC GCC AGC CCT 1307Tyr Val Ala Pro Asn Leu Gly Glu Val Pro Pr - #o His Ala Ser Pro# 400- GGC GGC TAC GTG ATG GAT TCA CGG CCA GGG CT - #T TAT GAT TCA GTG 1352Gly Gly Tyr Val Met Asp Ser Arg Pro Gly Le - #u Tyr Asp Ser Val# 415- CTG GTG CTG GAC TAT AAA AGC CTG TAC CCG TC - #G ATC ATC CGC ACC 1397Leu Val Leu Asp Tyr Lys Ser Leu Tyr Pro Se - #r Ile Ile Arg Thr# 430- TTT CTG ATT GAT CCC GTC GGG CTG GTG GAA GG - #C ATG GCG CAG CCT 1442Phe Leu Ile Asp Pro Val Gly Leu Val Glu Gl - #y Met Ala Gln Pro# 445- GAT CCA GAG CAC AGT ACC GAA GGT TTT CTC GA - #T GCC TGG TTC TCG 1487Asp Pro Glu His Ser Thr Glu Gly Phe Leu As - #p Ala Trp Phe Ser# 460- CGA GAA AAA CAT TGC CTG CCG GAG ATT GTG AC - #T AAC ATC TGG CAC 1532Arg Glu Lys His Cys Leu Pro Glu Ile Val Th - #r Asn Ile Trp His# 475- GGG CGC GAT GAA GCC AAA CGC CAG GGT AAC AA - #A CCG CTG TCG CAG 1577Gly Arg Asp Glu Ala Lys Arg Gln Gly Asn Ly - #s Pro Leu Ser Gln# 490- GCG CTG AAA ATC ATC ATG AAT GCC TTT TAT GG - #C GTG CTC GGC ACC 1622Ala Leu Lys Ile Ile Met Asn Ala Phe Tyr Gl - #y Val Leu Gly Thr# 505- ACC GCC TGC CGC TTC TTC GAT CCG CGG CTG GC - #A TCG TCG ATC ACC 1667Thr Ala Cys Arg Phe Phe Asp Pro Arg Leu Al - #a Ser Ser Ile Thr# 520- ATG CGT GGT CAT CAG ATC ATG CGG CAA ACC AA - #A GCG TTG ATT GAA 1712Met Arg Gly His Gln Ile Met Arg Gln Thr Ly - #s Ala Leu Ile Glu# 535- GCA CAG GGC TAC GAC GTT ATC TAC GGC GAT AC - #C GAC TCA ACG TTT 1757Ala Gln Gly Tyr Asp Val Ile Tyr Gly Asp Th - #r Asp Ser Thr Phe# 550- GTC TGG CTG AAA GGC GCA CAT TCG GAA GAA GA - #A GCG GCG AAA ATC 1802Val Trp Leu Lys Gly Ala His Ser Glu Glu Gl - #u Ala Ala Lys Ile# 565- GGT CGT GCA CTG GTG CAG CAC GTT AAC GCC TG - #G TGG GCG GAA ACG 1847Gly Arg Ala Leu Val Gln His Val Asn Ala Tr - #p Trp Ala Glu Thr# 580- CTG CAA AAA CAA CGG CTG ACC AGC GCA TTA GA - #A CTG GAG TAT GAA 1892Leu Gln Lys Gln Arg Leu Thr Ser Ala Leu Gl - #u Leu Glu Tyr Glu# 595- ACC CAT TTC TGC CGT TTT CTG ATG CCA ACC AT - #T CGC GGA GCC GAT 1937Thr His Phe Cys Arg Phe Leu Met Pro Thr Il - #e Arg Gly Ala Asp# 610- ACC GGC AGT AAA AAG CGT TAT GCC GGA CTG AT - #T CAG GAG GGC GAC 1982Thr Gly Ser Lys Lys Arg Tyr Ala Gly Leu Il - #e Gln Glu Gly Asp# 625- AAG CAG CGG ATG GTG TTT AAA GGG CTG GAA AC - #C GTG CGC ACC GAC 2027Lys Gln Arg Met Val Phe Lys Gly Leu Glu Th - #r Val Arg Thr Asp# 640- TGG ACG CCG CTG GCC CAG CAG TTT CAG CAG GA - #G CTA TAC CTG CGC 2072Trp Thr Pro Leu Ala Gln Gln Phe Gln Gln Gl - #u Leu Tyr Leu Arg# 655- ATC TTC CGC AAC GAG CCA TAT CAG GAA TAT GT - #A CGC GAA ACC ATC 2117Ile Phe Arg Asn Glu Pro Tyr Gln Glu Tyr Va - #l Arg Glu Thr Ile# 670- GAC AAA CTG ATG GCG GGT GAA CTG GAT GCG CG - #A CTG GTT TAC CGT 2162Asp Lys Leu Met Ala Gly Glu Leu Asp Ala Ar - #g Leu Val Tyr Arg# 685- AAA CGC CTT CGC CGT CCG CTG AGC GAG TAT CA - #G CGT AAT GTG CCG 2207Lys Arg Leu Arg Arg Pro Leu Ser Glu Tyr Gl - #n Arg Asn Val Pro# 700- CCT CAT GTA CGC GCC GCT CGC CTT GCC GAT GA - #A GAA AAC CAA AAG 2252Pro His Val Arg Ala Ala Arg Leu Ala Asp Gl - #u Glu Asn Gln Lys# 715- CGT GGT CGC CCC TTG CAA TAT CAG AAT CGC GG - #C ACC ATT AAG TAC 2297Arg Gly Arg Pro Leu Gln Tyr Gln Asn Arg Gl - #y Thr Ile Lys Tyr# 730- GTA TGG ACC ACC AAC GGC CCG GAG CCG CTG GA - #C TAC CAA CGT TCA 2342Val Trp Thr Thr Asn Gly Pro Glu Pro Leu As - #p Tyr Gln Arg Ser# 745- CCA CTG GAT TAC GAA CAC TAT CTG ACC CGC CA - #G CTA CAA CCC GTG 2387Pro Leu Asp Tyr Glu His Tyr Leu Thr Arg Gl - #n Leu Gln Pro Val# 760- GCG GAG GGA ATA CTC CCT TTT ATT GAG GAT AA - #T TTT GCT ACA CTT 2432Ala Glu Gly Ile Leu Pro Phe Ile Glu Asp As - #n Phe Ala Thr Leu# 775# 2459 TT GGG CTA TTT TGAMet Thr Gly Gln Leu Gly Leu Phe# 783 780- (2) INFORMATION FOR SEQ ID NO:6:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 783 base (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:- Val Ala Gln Ala Gly Phe Ile Leu Thr Arg Hi - #s Trp Arg Asp Thr# 15- Pro Gln Gly Thr Glu Val Ser Phe Trp Leu Al - #a Thr Asp Asn Gly# 30- Pro Leu Gln Val Thr Leu Ala Pro Gln Glu Se - #r Val Ala Phe Ile# 45- Pro Ala Asp Gln Val Pro Arg Ala Gln His Il - #e Leu Gln Gly Glu# 60- Gln Gly Phe Arg Leu Thr Pro Leu Ala Leu Ly - #s Asp Phe His Arg# 75- Gln Pro Val Tyr Gly Leu Tyr Cys Arg Ala Hi - #s Arg Gln Leu Met# 90- Asn Tyr Glu Lys Arg Leu Arg Glu Gly Gly Va - #l Thr Val Tyr Glu# 105- Ala Asp Val Arg Pro Pro Glu Arg Tyr Leu Me - #t Glu Arg Phe Ile# 120- Thr Ser Pro Val Trp Val Glu Gly Asp Met Hi - #s Asn Gly Thr Ile# 135- Val Asn Ala Arg Leu Lys Pro His Pro Asp Ty - #r Arg Pro Pro Leu# 150- Lys Trp Val Ser Ile Asp Ile Glu Thr Thr Ar - #g His Gly Glu Leu# 165- Tyr Cys Ile Gly Leu Glu Gly Cys Gly Gln Ar - #g Ile Val Tyr Met# 180- Leu Gly Pro Glu Asn Gly Asp Ala Ser Ser Le - #u Asp Phe Glu Leu# 195- Glu Tyr Val Ala Ser Arg Pro Gln Leu Leu Gl - #u Lys Leu Asn Ala# 210- Trp Phe Ala Asn Tyr Asp Pro Asp Val Ile Il - #e Gly Trp Asn Val# 225- Val Gln Phe Asp Leu Arg Met Leu Gln Lys Hi - #s Ala Glu Arg Tyr# 240- Arg Leu Pro Leu Arg Leu Gly Arg Asp Asn Se - #r Glu Leu Glu Trp# 255- Arg Asp Asp Gly Phe Lys Asn Gly Val Phe Ph - #e Ala Gln Ala Lys# 270- Gly Gly Leu Ile Ile Asp Gly Ile Glu Ala Le - #u Lys Ser Ala Phe# 285- Trp Asn Phe Ser Ser Phe Ser Leu Glu Thr Va - #l Ala Gln Glu Leu# 300- Leu Gly Glu Gly Lys Ser Ile Asp Asn Pro Tr - #p Asp Arg Met Asp# 315- Glu Ile Asp Arg Arg Phe Ala Glu Asp Lys Pr - #o Ala Leu Ala Thr# 330- Tyr Asn Leu Lys Asp Cys Glu Leu Val Thr Gl - #n Ile Phe His Lys# 345- Thr Glu Ile Met Pro Phe Leu Leu Glu Arg Al - #a Thr Val Asn Gly# 360- Leu Pro Val Asp Arg His Gly Gly Ser Val Al - #a Ala Phe Gly His# 375- Leu Tyr Phe Pro Arg Met His Arg Ala Gly Ty - #r Val Ala Pro Asn# 390- Leu Gly Glu Val Pro Pro His Ala Ser Pro Gl - #y Gly Tyr Val Met# 405- Asp Ser Arg Pro Gly Leu Tyr Asp Ser Val Le - #u Val Leu Asp Tyr# 420- Lys Ser Leu Tyr Pro Ser Ile Ile Arg Thr Ph - #e Leu Ile Asp Pro# 435- Val Gly Leu Val Glu Gly Met Ala Gln Pro As - #p Pro Glu His Ser# 450- Thr Glu Gly Phe Leu Asp Ala Trp Phe Ser Ar - #g Glu Lys His Cys# 465- Leu Pro Glu Ile Val Thr Asn Ile Trp His Gl - #y Arg Asp Glu Ala# 480- Lys Arg Gln Gly Asn Lys Pro Leu Ser Gln Al - #a Leu Lys Ile Ile# 495- Met Asn Ala Phe Tyr Gly Val Leu Gly Thr Th - #r Ala Cys Arg Phe# 510- Phe Asp Pro Arg Leu Ala Ser Ser Ile Thr Me - #t Arg Gly His Gln# 525- Ile Met Arg Gln Thr Lys Ala Leu Ile Glu Al - #a Gln Gly Tyr Asp# 540- Val Ile Tyr Gly Asp Thr Asp Ser Thr Phe Va - #l Trp Leu Lys Gly# 555- Ala His Ser Glu Glu Glu Ala Ala Lys Ile Gl - #y Arg Ala Leu Val# 570- Gln His Val Asn Ala Trp Trp Ala Glu Thr Le - #u Gln Lys Gln Arg# 585- Leu Thr Ser Ala Leu Glu Leu Glu Tyr Glu Th - #r His Phe Cys Arg# 600- Phe Leu Met Pro Thr Ile Arg Gly Ala Asp Th - #r Gly Ser Lys Lys# 615- Arg Tyr Ala Gly Leu Ile Gln Glu Gly Asp Ly - #s Gln Arg Met Val# 630- Phe Lys Gly Leu Glu Thr Val Arg Thr Asp Tr - #p Thr Pro Leu Ala# 645- Gln Gln Phe Gln Gln Glu Leu Tyr Leu Arg Il - #e Phe Arg Asn Glu# 660- Pro Tyr Gln Glu Tyr Val Arg Glu Thr Ile As - #p Lys Leu Met Ala# 675- Gly Glu Leu Asp Ala Arg Leu Val Tyr Arg Ly - #s Arg Leu Arg Arg# 690- Pro Leu Ser Glu Tyr Gln Arg Asn Val Pro Pr - #o His Val Arg Ala# 705- Ala Arg Leu Ala Asp Glu Glu Asn Gln Lys Ar - #g Gly Arg Pro Leu# 720- Gln Tyr Gln Asn Arg Gly Thr Ile Lys Tyr Va - #l Trp Thr Thr Asn# 735- Gly Pro Glu Pro Leu Asp Tyr Gln Arg Ser Pr - #o Leu Asp Tyr Glu# 750- His Tyr Leu Thr Arg Gln Leu Gln Pro Val Al - #a Glu Gly Ile Leu# 765- Pro Phe Ile Glu Asp Asn Phe Ala Thr Leu Me - #t Thr Gly Gln Leu# 780- Gly Leu Phe 783__________________________________________________________________________

Variant DNA polymerases

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Non-Patent Literature Citations (3)

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Entry
Reha-Krantz et al., Proc. Natl. Acad. Sci., 88:2417-2421, Mar. 1991.
Reha-Krantz et al., J. Mol. Biol., 189(2):262-272, May 1986.
Reha-Krantz, L.J., et al., "Bacteriophage T4 DNA Polymerase Mutations That Confer Sensitivity to the PP; Analog Phosphonoacetic Acid", J. Virol., 67(1):60-66 (1993).