Multiple drug resistance gene of Aspergillus fumigatus

TECHNICAL FIELD OF THE INVENTION
This invention relates to recombinant DNA technology. In particular, the invention concerns the cloning of nucleic acid encoding a multiple drug resistance protein of Aspergillus fumigatus.
BACKGROUND OF THE INVENTION
Multiple drug resistance (MDR) mediated by the human mdr-1 gene product was initially recognized during the course of developing regimens for cancer chemotherapy (Fojo et al., 1987, Journal of Clinical Oncology 5:1922-1927). A multiple drug resistant cancer cell line exhibits resistance to high levels of a large variety of cytotoxic compounds. Frequently these cytotoxic compounds will have no common structural features nor will they interact with a common target within the cell. Resistance to these cytotoxic agents is mediated by an outward directed, ATP-dependent pump encoded by the mdr-1 gene. By this mechanism, toxic levels of a particular cytotoxic compound are not allowed to accumulate within the cell.
MDR-like genes have been identified in a number of divergent organisms including numerous bacterial species, the fruit fly Drosophila melanogaster, Plasmodium falciparum, the yeast Saccharomyces cerevisiae, Caenorhabditis elegans, Leishmania donovanii, marine sponges, the plant Arabidopsis thaliana, as well as Homo sapiens. Extensive searches have revealed several classes of compounds that are able to reverse the MDR phenotype of multiple drug resistant human cancer cell lines rendering them susceptible to the effects of cytotoxic compounds. These compounds, referred to herein as "MDR inhibitors", include for example, calcium channel blockers, anti-arrhythmics, antihypertensives, antibiotics, antihistamines, immuno-suppressants, steroid hormones, modified steroids, lipophilic cations, diterpenes, detergents, antidepressants, and antipsychotics (Gottesman and Pastan, 1993, Annual Review of Biochemistry 62:385-427). Clinical application of human MDR inhibitors to cancer chemotherapy has become an area of intensive focus for research.
On another front, the discovery and development of antifungal compounds for specific fungal species has also met with some degree of success. Candida species represent the majority of fungal infections, and screens for new antifungal compounds have typically been designed to discover anti-Candida compounds. During development of antifungal agents, activity has generally been optimized based on activity against Candida albicans. As a consequence, these anti-Candida compounds frequently do not possess clinically significant activity against other fungal species such as Aspergillus fumigatus. However, it is interesting to note that at higher concentrations some anti-Candida compounds are able to kill Aspergillus fungal species. This suggests that the antifungal target(s) of these anti-Candida compounds is present in Aspergillus as well. Such results indicate that Aspergillus may possess a natural mechanism of resistance that permits them to survive in clinically relevant concentrations of antifungal compounds. Until the present invention, such a general mechanism of resistance to antifungal compounds in Aspergillus fumigatus has remained undescribed.
SUMMARY OF THE INVENTION
The invention provides, inter alia, isolated nucleic acid molecules that comprise nucleic acid encoding a multiple drug resistance protein from Aspergillus fumigatus, referred to herein as AfuMDR1, vectors encoding AfuMDR1, and host cells transformed with these vectors.
In another embodiment, the invention provides a method for determining the fungal MDR inhibition activity of a compound which comprises:
a) placing a culture of fungal cells, transformed with a vector capable of expressing AfuMDR1, in the presence of:
(i) an antifungal agent to which said fungal cell is resistant, but to which said fungal cell is sensitive in its untransformed state;
(ii) a compound suspected of possessing fungal MDR inhibition activity; and
b) determining the fungal MDR inhibition activity of said compound by measuring the ability of the antifungal agent to inhibit the growth of said fungal cell.

BRIEF DESCRIPTION OF THE FIGURES
The restriction enzyme site and function maps presented in the accompanying drawings are approximate representations of plasmids pPSM6, pPSM32, pPSM41, pPSM40, pPSM43, and pPSM42, discussed herein. The restriction enzyme site information is not exhaustive. There may be more restriction enzyme sites of a given type on the vectors than actually shown on the maps.
FIG. 1--A restriction enzyme site and function map of plasmid pPSM6.
FIG. 2--A restriction enzyme site and function map of plasmid pPSM32.
FIG. 3--A restriction enzyme site and function map of plasmid pPSM41.
FIG. 4--A restriction enzyme site and function map of plasmid pPSM40.
FIG. 5--A restriction enzyme site and function map of plasmid pPSM43.
FIG. 6--A restriction enzyme site and function map of plasmid pPSM42.

DETAILED DESCRIPTION OF THE INVENTION
The present invention provides isolated nucleic acid molecules that comprise a nucleic acid sequence encoding AfuMDR1. The amino acid sequence of AfuMDR1 is provided in the Sequence Listing as SEQ ID NO: 2. The cDNA (complementary deoxyribonucleic acid) sequence encoding AfuMDR1 is provided in the Sequence Listing as SEQ ID NO: 1. The genomic sequence encoding AfuMDR1 is provided as SEQ ID NO: 3.
Those skilled in the art will recognize that the degenerate nature of the genetic code enables one to construct many different nucleic acid sequences that encode the amino acid sequence of SEQ ID NO: 2. The cDNA sequence depicted by SEQ ID NO: 1 is only one of many possible AfuMDR1-encoding sequences. Consequently, the constructions described below and in the accompanying examples for the preferred nucleic acid molecules, vectors, and transformants of the invention are illustrative and are not intended to limit the scope of the invention.
All nucleotide and amino acid abbreviations used in this disclosure are those accepted by the United States Patent and Trademark Office as set forth in 37 C.F.R. .sctn.1.822(b)(1994).
The term "vector" refers to any autonomously replicating or integrating agent, including but not limited to plasmids, cosmids, and viruses (including phage), comprising a nucleic acid molecule to which one or more additional nucleic acid molecule can be added. Included in the definition of "vector" is the term "expression vector". Vectors are used either to amplify and/or to express deoxyribonucleic acid (DNA), either genomic or cDNA, or RNA (ribonucleic acid) which encodes AfuMDR1, or to amplify DNA or RNA that hybridizes with DNA or RNA encoding AfuMDR1.
The term "expression vector" refers to vectors which comprise a transcriptional promoter (hereinafter "promoter") and other regulatory sequences positioned to drive expression of a DNA segment that encodes AfuMDR1. Expression vectors of the present invention are replicable DNA constructs in which a DNA sequence encoding AfuMDR1 is operably linked to suitable control sequences capable of effecting the expression of AfuMDR1 in a suitable host. Such control sequences include a promoter, an optional operator sequence to control transcription, a sequence encoding suitable mRNA ribosomal binding sites, and sequences which control termination of transcription and translation. DNA regions are operably linked when they are functionally related to each other. For example, a promoter is operably linked to a DNA coding sequence if it controls the transcription of the sequence, or a ribosome binding site is operably linked to a coding sequence if it is positioned so as to permit translation.
The term "MDR inhibition activity" refers to the ability of a compound to inhibit the MDR activity of a host cell, thereby increasing the antifungal activity of an antifungal compound against said host cell.
In the present invention, AfuMDR1 may be synthesized by host cells transformed with vectors that provide for the expression of DNA encoding AfuMDR1. The DNA encoding AfuMDR1 may be the natural sequence or a synthetic sequence or a combination of both ("semi-synthetic sequence"). The in vitro or in vivo transcription and translation of these sequences results in the production of AfuMDR1. Synthetic and semi-synthetic sequences encoding AfuMDR1 may be constructed by techniques well known in the art. See Brown et al. (1979) Methods in Enzymology, Academic Press, N.Y., 68:109-151. AfuMDR1-encoding DNA, or portions thereof, may be generated using a conventional DNA synthesizing apparatus such as the Applied Biosystems Model 380A, 380B, 384 or 3848 DNA synthesizers (commercially available from Applied Biosystems, Inc., 850 Lincoln Center Drive, Foster City, Calif. 94404).
Owing to the natural degeneracy of the genetic code, the skilled artisan will recognize that a sizable yet definite number of nucleic acid sequences may be constructed which encode AfuMDR1. All such nucleic acid sequences are provided by the present invention. These sequences can be prepared by a variety of methods and, therefore, the invention is not limited to any particular preparation means. The nucleic acid sequences of the invention can be produced by a number of procedures, including DNA synthesis, cDNA cloning, genomic cloning, polymerase chain reaction (PCR) technology, or a combination of these approaches. These and other techniques are described by Maniatis, et al. Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. (1989), or Current Protocols in Molecular Biology (F. M. Ausubel et al., 1989 and supplements). The contents of both of these references are incorporated herein by reference.
In another aspect, this invention provides the genomic DNA encoding AfuMDR1. This DNA sequence is preferably obtained from plasmid pPSM6, described in Example 1. A restriction site and function map of pPSM6 is provided as FIG. 1 of the drawings. Plasmid pPSM6 comprises the ColE1 origin of replication (ColE1) which allows replication in Escherichia coli host cells, and the chloramphenicol resistance gene (CmR) for selection of E. coli cells transformed with the plasmid grown in the presence of chloramphenicol. The plasmid also contains the T7 promoter and the origin of replication from the f1 filamentous phage. The genomic DNA encoding AfuMDR1 can be obtained from plasmid pPSM6 on an approximately 7.1 kilobase pair HindIII/XbaI restriction enzyme fragment.
To effect the translation of AfuMDR1-encoding mRNA, one inserts the natural, synthetic, or semi-synthetic AfuMDR1-encoding DNA sequence into any of a large number of appropriate expression vectors through the use of appropriate restriction endonucleases and DNA ligases. Synthetic and semi-synthetic AfuMDR1-encoding DNA sequences can be designed, and natural AfuMDR1-encoding nucleic acid can be modified, to possess restriction endonuclease cleavage sites to facilitate isolation from and integration into these vectors. Particular restriction endonucleases employed will be dictated by the restriction endonuclease cleavage pattern of the expression vector utilized. Restriction enzyme sites are chosen so as to properly orient the AfuMDR1-encoding DNA with the control sequences to achieve proper in-frame translation of the AfuMDR1 molecule. The AfuMDR1-encoding DNA must be positioned so as to be in proper reading frame with the promoter and ribosome binding site of the expression vector, both of which are functional in the host cell in which AfuMDR1 is to be expressed.
Expression of AfuMDR1 in yeast cells, such as Saccharomyces cerevisiae is preferred. Suitable promoter sequences for use with yeast hosts include the promoters for 3-phosphoglycerate kinase (found on plasmid pAP12BD (ATCC 53231) and described in U.S. Pat. No. 4,935,350, Jun. 19, 1990) or other glycolytic enzymes such as enolase (found on plasmid pAC1 (ATCC 39532)), glyceraldehyde-3-phosphate dehydrogenase (derived from plasmid pHcGAPC1 (ATCC 57090, 57091)), hexokinase, pyruvate decarboxylase, phosphofructokinase, glucose-6-phosphate isomerase, 3-phosphoglycerate mutase, pyruvate kinase, triosephosphate isomerase, phosphoglucose isomerase, and glucokinase. Inducible yeast promoters have the additional advantage of transcription controlled by growth conditions. Such promoters include the promoter regions for alcohol dehydrogenase 2, isocytochrome C, acid phosphotase, degradative enzymes associated with nitrogen metabolism, metallothionein (contained on plasmid vector pCL28XhoLHBPV (ATCC 39475), U.S. Pat. No. 4,840,896), glyceraldehyde 3-phosphate dehydrogenase, and enzymes responsible for maltose and galactose utilization (GAL1 found on plasmid pRY121 (ATCC 37658) and on plasmid pPSM41, described below). Suitable vectors and promoters for use in yeast expression are further described by R. Hitzeman et al., in European Patent Publication No. 73,657A. Yeast enhancers such as the UAS Gal enhancer from Saccharomyces cerevisiae (found in conjunction with the CYC1 promoter on plasmid YEpsec--hI1beta, (ATCC 67024)), also are advantageously used with yeast promoters.
A variety of expression vectors useful in the present invention are well known in the art. For expression in Saccharomyces, the plasmid YRp7, for example, (ATCC-40053, Stinchcomb et al., 1979, Nature 282:39; Kingsman et al., 1979, Gene 7:141; Tschemper et al., 1980, Gene 10:157) is commonly used. This plasmid contains the trp gene which provides a selection marker for a mutant strain of yeast lacking the ability to grow in tryptophan, for example ATCC no. 44076 or PEP4-1 (Jones, 1977, Genetics 85:12).
Expression vectors useful in the expression of AfuMDR1 can be constructed by a number of methods. For example, the cDNA sequence encoding AfuMDR1 can be synthesized using DNA synthesis techniques such as those described above. Such synthetic DNA can be synthesized to contain cohesive ends that allow facile cloning into an appropriately digested expression vector. For example, the cDNA encoding AfuMDR1 can be synthesized to contain BamHI/XbaI cohesive ends. Such a synthetic DNA fragment can be ligated into a BamHI/XbaI-digested expression vector such as pYES-2 (Invitrogen Corp., San Diego Calif. 92121). The resultant plasmid is designated herein as pPSM41. Plasmid pPSM41 is useful for the expression of AfuMDR1 in Saccharomyces cerevisiae.
A plasmid related to pPSM41 can be constructed in the following manner. Logarithmic phase Aspergillus fumigatus mycelia are disrupted by grinding under liquid nitrogen according to the procedure of Minuth et al., 1982 (Current Genetics 5:227-231). Aspergillus fumigatus mRNA is preferably isolated from the disrupted mycelia using the QuickPrep.TM. mRNA Purification Kit (Pharmacia Biotech) according to the instructions of the manufacturer. cDNA is produced from the isolated mRNA using the TimeSaver.RTM. cDNA Synthesis Kit (Pharmacia Biotech) using oligo (dT) according to the procedure described by the manufacturer. In this process an EcoRI/NotI adapter (Stratagene, Inc.) is ligated to each end of the double stranded cDNA. The adapter modified cDNA is ligated into the vector Lambda Zap.sup.R II.RTM. using the Predigested Lambda Zap.sup.R II.RTM./EcoRI/CIAP Cloning Kit (Stratagene, Inc.) according to the instructions of the manufacturer to create a cDNA library.
The library is screened for full-length cDNA encoding AfuMDR1 using a .sup.32 P-radiolabeled fragment of the AfuMDR1 gene. This radiolabeled fragment is produced from the AfuMDR1 genomic DNA present in plasmid pPSM6. Utilizing the polymerase chain reaction (Gene Amp.RTM. Kit, Perkin Elmer Cetus, Norwalk, Conn.) and primers based upon the sequence presented as SEQ ID No. 1, a AfuMDR1 radiolabeled fragment is obtained. This radiolabeled fragment is used to probe the Aspergillus fumigatus cDNA library using standard hybridization techniques (Maniatis et al. 1992). In this manner, a full-length cDNA clone is recovered from the Aspergillus fumigatus cDNA library. A full-length cDNA clone recovered from the library is removed from the Lambda Zap.sup.R II vector by digestion with the restriction endonuclease NotI which produces an approximately 4100 base pair DNA fragment encoding AfuMDR1. The vector DNA fragment and the desired approximately 4100 base pair NotI DNA restriction fragment are separated by agarose gel electrophoresis. The desired approximately 4100 base pair NotI DNA fragment encoding AfuMDR1 is isolated by cutting out that portion of the agarose gel containing the fragment and electroeluting the DNA using a Centrilutor.TM. Micro-electroeluter (Amicon, Inc.) according to the manufacturer's instructions. The isolated approximately 4100 base pair NotI restriction fragment encoding AfuMDR1 is ligated to NotI digested pYES2 vector DNA. The correct orientation of the insert DNA is screened for by restriction endonuclease digestion using asymmetric sites located with the coding region and the flanking vector. The resultant plasmid is useful for the expression of AfuMDR1 in Saccharomyces cerevisiae.
A representation of plasmid pPSM41 is provided as FIG. 2. As noted above, this plasmid contains the AfuMDR1-encoding DNA operably linked to the Saccharomyces cerevisiae GAL1 promoter (P Gal1). Plasmid pPSM41 also comprises the yeast transcription terminator cyc1 (T cyc1) located in a position 3' to the AfuMDR1-encoding DNA. Plasmid pPSM41 further comprises the ColE1 origin of replication (ColE1) which allows replication in Escherichia coli host cells, and the ampicillin resistance gene (Amp) for selection of E. coli cells transformed with the plasmid grown in the presence of ampicillin. Plasmid pPSM41 further comprises the yeast 2.mu. origin of replication (2.mu. ori) allowing replication in yeast host cells, the yeast URA3 gene for selection of S. cerevisiae cells transformed with the plasmid grown in a medium lacking uracil, and the origin of replication from the f1 filamentous phage.
In a preferred embodiment of the invention Saccharomyces cerevisiae INVSc1 or INVSc2 cells (Invitrogen Corp., Sorrento Valley Blvd., San Diego Calif. 92121) are employed as host cells, but numerous other cell lines are available for this use. The transformed host cells are plated on an appropriate medium under selective pressure (minimal medium lacking uracil). The cultures are then incubated for a time and temperature appropriate to the host cell line employed.
The techniques involved in the transformation of yeast cells such as Saccharomyces cerevisiae cells are well known in the art and may be found in such general references as Ausubel et al., Current Protocols in Molecular Biology (1989), John Wiley & Sons, New York, N.Y. and supplements. The precise conditions under which the transformed yeast cells are cultured is dependent upon the nature of the yeast host cell line and the vectors employed.
In another application of this invention, plasmid pPSM40 (FIG. 4) is constructed which is similar to plasmid pPSM41 with the exception that a hemagglutinin tag (described in Example 4) is added to the 3' end of AfuMDR1. This immunological molecular handle is useful for protein purification, verification of protein production and cellular localization of the protein encoded by AfuMDR1.
Another preferred embodiment of this invention involves large scale production of AfuMDR1-encoded protein by expression in baculovirus. Two plasmids were constructed which permit expression of AfuMDR1 in baculovirus. The first plasmid, pPSM43 (FIG. 5), contains the polyhedron promoter (PpolH) of the Autographa californica nuclear polyhedrosis virus attached to AfuMDR1 plus other factors which allow infection of insect cells. The second plasmid (pPSM42, FIG. 6), constructed for baculovirus expression studies was nearly identical to pPSM43 except that it contained the hemagglutinin tag attached to the 3' end of AfuMDR1.
Nucleic acid, either RNA or DNA, which encodes AfuMDR1, or a portion thereof, is also useful in producing nucleic acid molecules useful in diagnostic assays for the detection of AfuMDR1 mRNA, AfuMDR1 cDNA, or AfuMDR1 genomic DNA. Further, nucleic acid, either RNA or DNA, which does not encode AfuMDR1, but which nonetheless is capable of hybridizing with AfuMDR1-encoding DNA or RNA is also useful in such diagnostic assays. These nucleic acid molecules may be covalently labeled by known methods with a detectable moiety such as a fluorescent group, a radioactive atom or a chemiluminescent group. The labeled nucleic acid is then used in conventional hybridization assays, such as Southern or Northern hybridization assays, or polymerase chain reaction assays (PCR), to identify hybridizing DNA, cDNA, or RNA molecules. PCR assays may also be performed using unlabeled nucleic acid molecules. Such assays may be employed to identify AfuMDR1 vectors and transformants and in in vitro diagnosis to detect AfuMDR1-like mRNA, cDNA, or genomic DNA from other organisms.
U.S. patent application Ser. No. 08/111680, now abandoned, the entire contents of which are hereby incorporated herein by reference, describes the use of combination therapy involving an antifungal agent possessing a proven spectrum of activity, with a fungal MDR inhibitor to treat fungal infections. This combination therapy approach enables an extension of the spectrum of antifungal activity for a given antifungal compound which previously had only demonstrated limited clinically relevant antifungal activity. Similarly, compounds with demonstrated antifungal activity can also be potentiated by a fungal MDR inhibitor such that the antifungal activity of these compounds is extended to previously resistant species. To identify compounds useful in such combination therapy the present invention provides an assay method for identifying compounds with Aspergillus fumigatus MDR inhibition activity. Host cells that express AfuMDR1 provide an excellent means for the identification of compounds useful as inhibitors of Aspergillus fumigatus MDR activity. Generally, the assay utilizes a culture of a fungal cell transformed with a vector which provides expression of AfuMDR1. The expression of AfuMDR1 by the host cell enables the host cell to grow in the presence of an antifungal compound to which the fungal cell is sensitive to in the untransformed state. Thus, the transformed fungal cell culture is grown in the presence of i) an antifungal agent to which the untransformed fungal cell is sensitive, but to which the transformed host cell is resistant, and ii) a compound that is suspected of being an MDR inhibitor. The effect of the suspected MDR inhibitor is measured by testing for the ability of the antifungal compound to inhibit the growth of the transformed fungal cell. Such inhibition will occur if the suspected Aspergillus fumigatus MDR inhibitor blocks the ability of AfuMDR1 to prevent the antifungal compound from acting on the fungal cell. An illustrative example of such an assay is provided in Example 7.
In order to illustrate more fully the operation of this invention, the following examples are provided, but are not to be construed as a limitation on the scope of the invention.
EXAMPLE 1
Source of the AfuMDR1 encoding Genomic DNA of Aspergillus fumigatus
Construction of plasmid pPSM6 containing AfuMDR1
An approximately 7100 bp HindIII-XbaI fragment of genomic DNA containing AfuMDR1 from Aspergillus fumigatus may be obtained in the following manner. Some adjustment may be required if a different strain of Aspergillus fumigatus is used than that used by Applicants, which was 10AF/86/10 (Denning and Stevens, Antimicrob. Agents and Chemother. 35:1329-1333). Total DNA is isolated from logarithmic phase Aspergillus fumigatus mycelia by grinding under liquid nitrogen according to the procedure of Minuth et al., 1982 (Current Genetics 5:227-231). The DNA is cleaved with the restriction endonucleases HindIII and XbaI, electrophoresed through a 0.8% agarose gel and the DNA fragments produced corresponding to approximately 6500 to 7500 bp are isolated by electroelution (Centriluter.TM. Micro-electroeluter, Amicon, Inc.). The isolated fragments are ligated into the commercially available plasmid vector pBC SK(-) (Stratagene Inc., LaJolla, Calif.) after digestion with HindIII and XbaI. Transformant colonies produced by this cloning process are screened for the presence of AfuMDR1 using a hybridization probe comprised of a significant portion of the AfuMDR1 gene produced by PCR using the following primers according to the manufacturers instructions: 5'-GCTCGTTGAGAATGCGGCCAG-3' (SEQ ID NO: 4) and 5'-ACTTGGTATCCAAAGCTGATG-3' (SEQ ID NO: 5). The resultant plasmid, pPSM6, is subjected to restriction endonuclease digestion and analysis by agarose gel electrophoresis. A representation of plasmid pPSM6 is provided as FIG. 1.
EXAMPLE 2
Expression of AfuMDR1 in Aspergillus montevidensis
Aspergillus montevidensis (ATTCC #10077) is susceptible to a wide range of antifungal compounds, suggesting the lack of an effective efflux mechanism(s) for such compounds. Functional expression of AfuMDR1 in such a strain will produce an antifungal resistant phenotype and provides a useful strain for screening for inhibition of AfuMDR1. Expression of AfuMDR1 in such a related Aspergillus species avoids problems presented by the presence of introns within this gene (i.e. splicing of introns should be similar in these species) and promoter recognition.
Construction of plasmid pPSM32 for the expression of AfuMDR1 in Aspergillus montevidensis
The present example utilizes a selectable marker for transformation of Aspergillus montevidensis comprised of the hygromycin B phosphotransferase (HPT) gene (Kaster et al., 1984, Current Genetics, 8:353-358) operably linked to the Aspergillus nidulans amds promoter (P-amdS) (Hynes et al., 1983, Molecular and Cellular Biology, 3:1430-1439). Those skilled in the art will recognize that this promoter/selectable marker combination may be assembled in a number of ways. In one instance, PCR is used to generate P-amdS and HPT independently which are ligated together to form the operable selectable marker with for example HindIII restriction sites at both termini. In our case this process produces an approximately 4,000 bp HindIII fragment carrying the operable selectable marker.
Plasmid pPSM6 is linearized by restriction endonuclease digestion with HindIII. The resultant approximately 10,500 bp DNA fragment is ligated to the approximately 4,000 base pair HindIII DNA fragment encoding HPT. The resultant plasmid, pPSM32, is subjected to restriction endonuclease digestion and analysis by agarose gel electrophoresis. Plasmid pPSM32, represented in FIG. 2, is suitable for the expression of AfuMDR1 in Aspergillus montevidensis.
EXAMPLE 3
Expression of the AfuMDR1 gene in Saccharomyces cerevisiae
Expression of the AfuMDR1 gene in eukaryotic cells other than Aspergillus (or other closely related species capable of utilizing endogenous AfuMdR1 promoter and terminator sequences) is accomplished by the removal of endogenous AfuMDR1 promoter and terminator DNA sequences and their replacement with promoter and terminator DNA sequences compatible with gene expression in the host of choice.
Construction of plasmid pPSM41 for expression of AfuMDR1 in Saccharomyces cerevisiae
Total A. fumigatus mRNA is isolated from disrupted mycelia using the QuickPrep.TM. mRNA purification Kit (Pharmacia Biotech) using oligo (dT) according to the procedure described by the manufacturer. First strand cDNA synthesis is accomplished using the Superscrip.TM. Preamplification System (GibcoBRL/Life Technologies) according to the procedure described by the manufacturer. The resultant cDNA is used as template in an amplification process using the polymerase chain reaction. Utilizing cloned Pfu DNA Polymerase (Stratagene) in the polymerase chain reaction and the following primers: TBN-76 (5'-GCGCGGATCCGCAACATGCCTGCGCCTG-3') (SEQ ID NO: 6) and TBN-77 (5'-GGAATGATTAATGAGTCTTTC-3') (SEQ ID NO: 7), an approximately 4,100 base pair DNA fragment encoding AfuMDR1 is amplified. The resultant fragment is subjected to restriction endonuclease digestion with BamHI and XbaI, and subjected to agarose gel electrophoresis. The desired approximately 4100 base pair BamHI-XbaI DNA fragment encoding AfuMDR1 is isolated by excising that portion of the agarose gel containing the fragment and electroeluting the DNA using a Centriluter.TM. Micro-electroeluter (Amicon, Inc.) according to the manufacturer's instructions. The resultant approximately 4,100 base pair BamHI-XbaI DNA fragment is ligated to BamHI and XbaI-digested plasmid pYES2 vector DNA (Invitrogen Corp., San Diego, Calif.). The resultant plasmid, pPSM41, is useful for the expression of AfuMDR1 in Saccharomyces cerevisiae.
A representation of plasmid pPSM41 is provided as FIG. 3. As noted above, this plasmid contains the AfuMDR1-encoding DNA operably linked to the Saccharomyces cerevisiae GAL1 promoter (P Gal1). Plasmid pPSM41 also comprises the yeast transcription terminator cyc1 (T cyC1) located in a position 3' to the AfuMDR1-encoding DNA. Plasmid pPSM41 further comprises the ColE1 origin of replication (ColE1) which allows replication in Escherichia coli host cells, and the ampicillin resistance gene (Amp) for selection of E. coli cells transformed with the plasmid grown in the presence of ampicillin. Plasmid pPSM41 further comprises the yeast 2.mu. origin of replication (2.mu. ori) allowing replication in yeast host cells, the yeast URA3 gene for selection of S. cerevisiae cells transformed with the plasmid grown in a medium lacking uracil, and the origin of replication from the f1 filamentous phage.
In a preferred embodiment of the invention Saccharomyces cerevisiae INVSc1 or INVSc2 cells (Invitrogen Corp., Sorrento Valley Blvd., San Diego Calif. 92121) are employed as host cells, but numerous other cell lines are available for this use. The transformed host cells are plated on an appropriate medium under selective pressure (minimal medium lacking uracil). The cultures are then incubated for a time and temperature appropriate to the host cell line employed.
The techniques involved in the transformation of yeast cells such as Saccharomyces cerevisiae cells are well known in the art and may be found in such general references as Ausubel et al., Current Protocols in Molecular Biology (1989), John Wiley & Sons, New York, N.Y. and supplements. The precise conditions under which the transformed yeast cells are cultured is dependent upon the nature of the yeast host cell line and the vectors employed.
Saccharomyces cerevisiae INVSc1 cells (Invitrogen Corp., San Diego Calif. 92191) are transformed with the plasmid pPSM41 by the technique described by J. D. Beggs, 1988, Nature 275:104-109). The transformed yeast cells are grown in a broth medium containing YNB/CSM-Ura/raf (YNB/CSM-Ura �Yeast Nitrogen Base (Difco Laboratories, Detroit, Mich.) supplemented with CSM-uRA (Bio 101, Inc.)! supplemented with 4% raffinose) at 28.degree. C. in a shaker incubator until the culture is saturated. To induce expression of AfuMDR1, a portion of the culture is used to inoculate a flask containing YNB/CSM-Ura medium supplemented with 2% galactose (YNB/CSM-Ura/gal) rather than raffinose as the sole carbon source. The inoculated flask is incubated at 28.degree. C. for about 16 hours.
EXAMPLE 4
Expression of the AfuMDR1/HA fusion in Saccharomyces cerevisiae
During the course of expression studies it would be useful to have an easily detected molecular handle attached to the protein expressed by AfuMDR1. This molecular tag would useful in detection of protein produced, purification of protein, and localization of protein within the cell expressing AfuMDR1.
Construction of plasmid pPSM40 containing a HA tag
To facilitate the detection and purification of the protein encoded by AfuMDR1, a gene encoding a fusion protein is constructed. A sequence encoding a peptide antigenic to a commercially available antibody may effectively be added in-frame to either the NH-terminus or the COOH-terminus of the encoded AfuMDR1 sequence. In the present example, a COOH-terminal fusion to AfuMDR1 using an encoded hemagglutanin (HA) flu epitope tag YPYDVPDYA is described, however, the specific constructions described herein are in no way intended to limit the scope of the invention. Polyclonal Rabbit Antibody, HA.11, is purchased from Berkeley Antibody Company (Richmond, Calif.), and may be used for epitope tagging and protein surveilance according to the recommendations of the manufacturer.
The approximately 4100 base pair BamHI-XbaI DNA fragment encoding Afu-mdr1 (vide supra) contains an AseI restriction site which overlaps with the encoded termination codon of AfuMDR1. The fragment is subjected to restriction enzyme digestion with AseI, and ligated to a DNA linker comprised of the annealed oligonucleotides TBN-78 (5'-TACCCATACGACGTCCCAGACTACGCTTGATAAT-3') (SEQ ID NO: 8) and TBN-79 (5'-CTAGATTATCAAGCGTAGTCTGGGACGTCGTATGGG-3') (SEQ ID NO: 9). The DNA linker encodes the hemagglutanin flu epitope tag YPYDVPDYA. The resultant DNA fragment is subjected to restriction enzyme digestion with XbaI and subjected to agarose gel electrophoresis. The desired approximately 4100 base pair BamHI-XbaI DNA fragment encoding the Afu-mdr1/HA fusion is isolated by excising that portion of the agarose gel containing the fragment and electroeluting the DNA using a Centriluter.TM. Micro-electroeluter (Amicon, Inc.) according to the manufacturer's instructions. The resultant approximately 4100 base pair BamHI-XbaI DNA fragment is ligated to BamHI and XbaI-digested plasmid pYES2 vector DNA (Invitrogen Corp., San Diego, Calif.). The resultant plasmid, pPSM40, is useful for the expression of the AfuMDR1/HA in Saccharomyces cerevisiae. A representation of plasmid pPSM40 is provided as FIG. 4.
EXAMPLE 5
Expression of the AfuMDR1 gene in Baculovirus Systems
The desired approximately 4100 base pair BamHI-XbaI DNA fragment encoding Afu-mdr1 cDNA is prepared via the polymerase chain reaction and purified as described in Example 3 (vide supra). The approximately 4100 base pair BamHI-XbaI DNA fragment is ligated to BamHI-XbaI digested plasmid pFASTBAc-1 (GibcoBRL/Life Technologies, Gaithersburg, Md.). The resultant plasmid, pPSM43, is useful for the expression of AfuMDR1 in the BAC-TO-BAC.TM. Baculovirus Expression System (Gibco-BRL/Life Technologies). A restriction map and function map of plasmid pFASTBAc-1 is provided on page 5 of the GibcoBRL/Life Technologies Catalog Number 10359-016 (Instruction Manual--BAC-TO-BAC.TM. Baculovirus Expression System). The catalogue is herein incorporated by reference.
A representation of plasmid pPSM43 is provided as FIG. 5. This plasmid contains the Afumdr1-encoding DNA operably linked to the polyhedrin promoter (P.sub.polh) of the Autographa californica nuclear polyhedrosis virus (AcNPV). Plasmid pPSM43 also comprises a simian virus 40 (SV40) poly(A) transcription terminator located in a position 3' to the AfuMDR1 encoding DNA.
Transposition of pPSM43 into DH10Bac10 is conducted in accordance with the teachings of page 8 of GibcoBRL/Life Technologies Catalog Number 10359-016. Competent cells are provided as part of the expression kit accompanying pFASTBAC-1 in Catalog Number 10359-016.
Isolation of recombinant Bacmid DNA is accomplished in accordance with the teachings of pages 8 and 9 of GibcoBRL/Life Technologies Catalog Number 10359-016.
Transfection of Spodoptera frugiperda (Sf9) cells (ATCC #CRL 1711) with recombinant Bacmid DNA, harvest, and storage of the recombinant Baculovirus, and infection of insect cells with recombinant Baculovirus particles is accomplished in accordance with the teachings of pages 9 and 10 of GibcoBRL/Life Technologies Catalog Number 10359-016.
EXAMPLE 6
Expression of the AfuMDR1/HA fusion in Baculovirus Systems
The desired approximately 4100 base pair BamHI-XbaI cDNA fragment encoding the Afu-mdr1/HA fusion (see Example 3) is ligated to BamHI-XbaI digested plasmid pFASTBAc-1 (GibcoBRL/Life Technologies, Gaithersburg, Md.). The resultant plasmid, pPSM42 (illustrated in FIG. 6), is useful for the expression of Afu-mdr1/HA fusion in the BAC-TO-BAC.TM. Baculovirus Expression System (Gibco-BRL/Life Technologies), in substantial accordance with the methods as described above.
EXAMPLE 7
Antifungal Potentiator Assay Using Saccharomyces cerevisiae
Approximately 1.times.10.sup.6 cells of a Saccharomyces cerevisiae INVSc1/pPSM41 culture are delivered to each of several agar plates containing YNB/CSM-Ura/gal. The agar surface is allowed to dry in a biohazard hood. Saccharomyces cerevisiae INVSc1/pPSM41 cells express the AfuMDR1 activity.
An antifungal compound that the untransformed yeast cell is typically sensitive to, such as R106I (U.S. Pat. No. 5,057,493, which is hereby incorporated herein by reference), is dissolved in 100% ethanol at a concentration of either 1 or 7 mg/ml. Twenty .mu.l of the 1 mg/ml solution is delivered to an antibiotic susceptibility test disc (Difco Laboratories, Detroit, Mich.). After addition of the antifungal solution the disc is allowed to air dry in a biohazard hood. When dry, the disc is placed on the surface of the petri plates containing the Saccharomyces cerevisiae INVSc1/pPSM41 cells.
Compounds to be tested for the ability to inhibit AfuMDR1 are dissolved in dimethylsulfoxide (DMSO). The amount of compound added to the DMSO depends on the solubility of the individual compound to be tested. Twenty .mu.l of the suspensions containing a compound to be tested are delivered to an antibiotic susceptibility test disc (Difco Laboratories, Detroit, Mich.). The disc is then placed on the surface of the dried petri plates containing the Saccharomyces cerevisiae INVSc1/pPSM41 cells approximately 2 cm from the antifungal-containing disc. Petri plates containing the two discs are incubated at 28.degree. C. for about 16-48 hours.
Following this incubation period, the petri plates are examined for zones of growth inhibition around the discs. A zone of growth inhibition near the antifungal disc on the test plate indicates that the compound being tested for MDR inhibition activity blocks the activity of AfuMDR1 and allows the antifungal compound to inhibit the growth of the yeast host cell. Such compounds are said to possess MDR inhibition activity. Little or no zone of growth inhibition indicates that the test compound does not block MDR activity and, thus, AfuMDR1 is allowed to act upon the antifungal compound to prevent its activity upon the host cell.
EXAMPLE 8
Approximately one million cells of Aspergillus montevidensis, transformed with pPSM32, are delivered to the surface of several agar plates containing a rich growth medium. These cells express AfuMDR1. Assessment of anti-fungal potentiator activity of a battery of compounds is then performed as stated in Example 7.
__________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 9- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 4047 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 1..4047- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:- ATG CCT GCG CCT GAA ACC GGC GCC TCC TCT CG - #G GAG AAG TCC CTC GAG 48Met Pro Ala Pro Glu Thr Gly Ala Ser Ser Ar - #g Glu Lys Ser Leu Glu# 15- GAT TTG CAA GTA GCG ACA TTG GAG AAA GGA CG - #T TCC ACT TCA TCT TCC 96Asp Leu Gln Val Ala Thr Leu Glu Lys Gly Ar - #g Ser Thr Ser Ser Ser# 30- GGT GCC GAC AAT GAA AAG CCA CAC GAC CAT CA - #T TCG TTA TCG GAC ACG 144Gly Ala Asp Asn Glu Lys Pro His Asp His Hi - #s Ser Leu Ser Asp Thr# 45- ATC ATG GCG CCT CCA GAT GGC AAG AAA AAG GA - #T CAC GGG AAA GCT GTC 192Ile Met Ala Pro Pro Asp Gly Lys Lys Lys As - #p His Gly Lys Ala Val# 60- GAC CTG AAC GAT GAT TCT CTC TTT GCC CAT CT - #C CAG GAG CAC GAG AAA 240Asp Leu Asn Asp Asp Ser Leu Phe Ala His Le - #u Gln Glu His Glu Lys# 80- GAG GTA CTC AAG CGA CAG CTT GAT GCA CCG TC - #T GTG AAA GTC TCT TTC 288Glu Val Leu Lys Arg Gln Leu Asp Ala Pro Se - #r Val Lys Val Ser Phe# 95- TTC ACT TTG TAT CGC TAT GCC TCG AGA AAG GA - #C ATC CTG ATC ATA CTC 336Phe Thr Leu Tyr Arg Tyr Ala Ser Arg Lys As - #p Ile Leu Ile Ile Leu# 110- GTG AGC GCA ATC TGT GCT ATT GCT GCT GGT GC - #C GCT CTT CCC TTG TTC 384Val Ser Ala Ile Cys Ala Ile Ala Ala Gly Al - #a Ala Leu Pro Leu Phe# 125- ACA ATT CTC TTC GGT TCA CTA GCC TCA GCG TT - #C CAG GGC ATA TCT CTG 432Thr Ile Leu Phe Gly Ser Leu Ala Ser Ala Ph - #e Gln Gly Ile Ser Leu# 140- GGT ACT ATG CCC TAT CAT GAG TTC TAT CAC AA - #A CTG ACT AAG AAT GTG 480Gly Thr Met Pro Tyr His Glu Phe Tyr His Ly - #s Leu Thr Lys Asn Val145 1 - #50 1 - #55 1 -#60- CTT TAC TTT GTG TAT CTC GGT ATT GCC GAG TT - #T GTC ACA GTC TAT GTC 528Leu Tyr Phe Val Tyr Leu Gly Ile Ala Glu Ph - #e Val Thr Val Tyr Val# 175- AGC ACC GTG GGT TTC ATT TAT ACT GGC GAA CA - #T CTC ACA CAG AAG ATC 576Ser Thr Val Gly Phe Ile Tyr Thr Gly Glu Hi - #s Leu Thr Gln Lys Ile# 190- CGT GAA AAT TAT CTT GAG GCT ATC CTG AGG CA - #G AAT ATG GCT TAC TTC 624Arg Glu Asn Tyr Leu Glu Ala Ile Leu Arg Gl - #n Asn Met Ala Tyr Phe# 205- GAC AAG TTG GGC GCC GGT GAA GTT ACC ACG CG - #T ATC ACT GCT GAT ACC 672Asp Lys Leu Gly Ala Gly Glu Val Thr Thr Ar - #g Ile Thr Ala Asp Thr# 220- AAC CTG ATC CAG GAC GCC ATC TCT GAG AAA GT - #T GGT CTC ACT TTG ACC 720Asn Leu Ile Gln Asp Ala Ile Ser Glu Lys Va - #l Gly Leu Thr Leu Thr225 2 - #30 2 - #35 2 -#40- GCA TTC GCC ACA TTT GTA ACC GCA TTT ATT GT - #C GCC TAC GTC AAG TAT 768Ala Phe Ala Thr Phe Val Thr Ala Phe Ile Va - #l Ala Tyr Val Lys Tyr# 255- TGG AAG TTG GCT CTG ATC TGT ACC TCA ACT AT - #C GTC GCG CTG GTC ATG 816Trp Lys Leu Ala Leu Ile Cys Thr Ser Thr Il - #e Val Ala Leu Val Met# 270- GTT ATG GGA GGT GGG TCG AGG TTT ATT GTG AA - #G TAC AGC AAG AAA TCT 864Val Met Gly Gly Gly Ser Arg Phe Ile Val Ly - #s Tyr Ser Lys Lys Ser# 285- ATT GAA AGT TAT GGT GCT GGT GGA ACT GTC GC - #G GAA GAA GTC ATC AGC 912Ile Glu Ser Tyr Gly Ala Gly Gly Thr Val Al - #a Glu Glu Val Ile Ser# 300- TCC ATT CGG AAT GCT ACC GCT TTC GGC ACT CA - #G GAT AAG CTC GCC AAG 960Ser Ile Arg Asn Ala Thr Ala Phe Gly Thr Gl - #n Asp Lys Leu Ala Lys305 3 - #10 3 - #15 3 -#20- CAA TAC GAA ACC CAT CTG GCT GAG GCT GAA AA - #A TGG GGC GTC AAA CAA1008Gln Tyr Glu Thr His Leu Ala Glu Ala Glu Ly - #s Trp Gly Val Lys Gln# 335- CAG GTC ATC CTT GGT ATG ATG ATT GGT GGT AT - #G TTC GGT ATC ATG TTC1056Gln Val Ile Leu Gly Met Met Ile Gly Gly Me - #t Phe Gly Ile Met Phe# 350- TCG AAC TAT GGT CTC GGT TTC TGG ATG GGA TC - #T CGC TTC GTT GTC GGT1104Ser Asn Tyr Gly Leu Gly Phe Trp Met Gly Se - #r Arg Phe Val Val Gly# 365- AAA GAA GTC AAC GTG GGC CAA GTT CTG ACA GT - #T TTG ATG TCT ATC CTG1152Lys Glu Val Asn Val Gly Gln Val Leu Thr Va - #l Leu Met Ser Ile Leu# 380- ATC GGT TCG TTC AGT TTG GGC AAC GTC GCC CC - #C AAT GGT CAG GCC TTT1200Ile Gly Ser Phe Ser Leu Gly Asn Val Ala Pr - #o Asn Gly Gln Ala Phe385 3 - #90 3 - #95 4 -#00- ACG AAT GGT GTT GCT GCG GCC GCG AAG ATT TA - #C AGC ACG ATT GAC CGC1248Thr Asn Gly Val Ala Ala Ala Ala Lys Ile Ty - #r Ser Thr Ile Asp Arg# 415- AGA TCG CCA CTG GAC CCC TAT TCT GAC GAA GG - #G AAG GTA CTC GAC CAT1296Arg Ser Pro Leu Asp Pro Tyr Ser Asp Glu Gl - #y Lys Val Leu Asp His# 430- TTT GAA GGA AAT ATC GAA TTT CGC AAT GTC AA - #A CAC ATC TAC CCT TCA1344Phe Glu Gly Asn Ile Glu Phe Arg Asn Val Ly - #s His Ile Tyr Pro Ser# 445- AGA CCC GAA GTT ACA GTC ATG GAA GAT GTC TC - #T TTA TCG ATG CCC GCC1392Arg Pro Glu Val Thr Val Met Glu Asp Val Se - #r Leu Ser Met Pro Ala# 460- GGA AAG ACT ACC GCA TTG GTG GGC CCA TCT GG - #C TCT GGA AAG AGT ACT1440Gly Lys Thr Thr Ala Leu Val Gly Pro Ser Gl - #y Ser Gly Lys Ser Thr465 4 - #70 4 - #75 4 -#80- GTT GTC GGC TTG GTG GAG CGC TTT TAC CTT CC - #A GTA GGA GGC CAG GTA1488Val Val Gly Leu Val Glu Arg Phe Tyr Leu Pr - #o Val Gly Gly Gln Val# 495- TTG CTG GAC GGC CAT GAT ATC CAA ACC CTC AA - #C CTC CGT TGG CTG CGA1536Leu Leu Asp Gly His Asp Ile Gln Thr Leu As - #n Leu Arg Trp Leu Arg# 510- CAG CAG ATC TCT CTT GTC AGC CAG GAA CCT GT - #T CTT TTC AGC ACC ACG1584Gln Gln Ile Ser Leu Val Ser Gln Glu Pro Va - #l Leu Phe Ser Thr Thr# 525- ATC TTT AGA AAC ATC GAA CAT GGC TTG ATT GG - #C ACC AAA TTC GAG CAT1632Ile Phe Arg Asn Ile Glu His Gly Leu Ile Gl - #y Thr Lys Phe Glu His# 540- GAG TCG AAG GAC AAG ATT AGA GAG CTC GTT GA - #G AAT GCG GCC AGA ATG1680Glu Ser Lys Asp Lys Ile Arg Glu Leu Val Gl - #u Asn Ala Ala Arg Met545 5 - #50 5 - #55 5 -#60- GCC AAT GCT CAT GAT TTT ATT ATG GCT CTG CC - #T GAA GGT TAC GAT ACG1728Ala Asn Ala His Asp Phe Ile Met Ala Leu Pr - #o Glu Gly Tyr Asp Thr# 575- AAT GTG GGT CAG CGT GGT TTC TTA CTT TCA GG - #A GGT CAG AAG CAA CGT1776Asn Val Gly Gln Arg Gly Phe Leu Leu Ser Gl - #y Gly Gln Lys Gln Arg# 590- ATT GCC ATT GCT CGT GCC ATT GTC AGT GAC CC - #C AAG ATT CTG TTG CTT1824Ile Ala Ile Ala Arg Ala Ile Val Ser Asp Pr - #o Lys Ile Leu Leu Leu# 605- GAT GAA GCT ACA TCA GCT TTG GAT ACC AAG TC - #C GAG GGC GTC GTC CAA1872Asp Glu Ala Thr Ser Ala Leu Asp Thr Lys Se - #r Glu Gly Val Val Gln# 620- GCC GCT CTT GAT AAA GCT GCC GAG GGT AGA AC - #T ACC ATT GTC ATT GCT1920Ala Ala Leu Asp Lys Ala Ala Glu Gly Arg Th - #r Thr Ile Val Ile Ala625 6 - #30 6 - #35 6 -#40- CAC CGT TTG TCA ACA ATC AAA ACA GCC CAC AA - #C ATT GTT GCC ATG GTC1968His Arg Leu Ser Thr Ile Lys Thr Ala His As - #n Ile Val Ala Met Val# 655- GGC GGA AAG ATT GCC GAA CAG GGA ACA CAT GA - #C GAA TTG GTC GAT CGC2016Gly Gly Lys Ile Ala Glu Gln Gly Thr His As - #p Glu Leu Val Asp Arg# 670- AAA GGC ACG TAC TAT AAA CTT GTG GAG GCG CA - #A CGT ATC AAC GAG GAG2064Lys Gly Thr Tyr Tyr Lys Leu Val Glu Ala Gl - #n Arg Ile Asn Glu Glu# 685- AAG GAA GCA GAA GCT CTG GAA GCC GAC GCC GA - #C ATG GAC GCC GAT GAT2112Lys Glu Ala Glu Ala Leu Glu Ala Asp Ala As - #p Met Asp Ala Asp Asp# 700- TTT GGT CAA GAA GGG GTT ACT CGC ATC AAG AC - #T GCA GTT AGC AGC TCG2160Phe Gly Gln Glu Gly Val Thr Arg Ile Lys Th - #r Ala Val Ser Ser Ser705 7 - #10 7 - #15 7 -#20- AAT TCT CTC GAT GCT GTA GAT GAG AAG GCG CG - #C TTG GAG ATG AAG CGA2208Asn Ser Leu Asp Ala Val Asp Glu Lys Ala Ar - #g Leu Glu Met Lys Arg# 735- ACC GGA ACG CAA AAA TCG GTT TCG AGT GCC GT - #T CTA TCT AAG AAA GTC2256Thr Gly Thr Gln Lys Ser Val Ser Ser Ala Va - #l Leu Ser Lys Lys Val# 750- CCC GAG CAG TTC GAG AAG TAT TCA CTC TGG AC - #C CTC GTC AAG TTC ATC2304Pro Glu Gln Phe Glu Lys Tyr Ser Leu Trp Th - #r Leu Val Lys Phe Ile# 765- GGT GCA TTT AAC CGC CCT GAG CTT GGT TAC AT - #G CTC ATT GGC TTG ACT2352Gly Ala Phe Asn Arg Pro Glu Leu Gly Tyr Me - #t Leu Ile Gly Leu Thr# 780- TTC TCG TTC CTT GCC GGT GGT GGT CAA CCT AC - #C CAG GCT TTT CTG TAC2400Phe Ser Phe Leu Ala Gly Gly Gly Gln Pro Th - #r Gln Ala Phe Leu Tyr785 7 - #90 7 - #95 8 -#00- GCC AAG GCA ATT AGC ACG CTC TCG TTA CCC GA - #A TCA ATG TTT CAC AAA2448Ala Lys Ala Ile Ser Thr Leu Ser Leu Pro Gl - #u Ser Met Phe His Lys# 815- CTC AGG CAT GAC GCG AAT TTC TGG TCC TTG AT - #G TTC TTC GTG GTT GGA2496Leu Arg His Asp Ala Asn Phe Trp Ser Leu Me - #t Phe Phe Val Val Gly# 830- ATT GCT CAA TTT ATC AGC CTG TCT ATC AAT GG - #T ACA GCA TTT GCT ATT2544Ile Ala Gln Phe Ile Ser Leu Ser Ile Asn Gl - #y Thr Ala Phe Ala Ile# 845- TGT TCG GAG AGA CTC ATT CGC CGA GCT AGA AG - #T CAA GCG TTT AGA TCG2592Cys Ser Glu Arg Leu Ile Arg Arg Ala Arg Se - #r Gln Ala Phe Arg Ser# 860- ATT CTT CGT CAG GAC ATC TCA TTT TTC GAC AG - #G GAA GAG AAC AGC ACC2640Ile Leu Arg Gln Asp Ile Ser Phe Phe Asp Ar - #g Glu Glu Asn Ser Thr865 8 - #70 8 - #75 8 -#80- GGT GCC TTG ACG TCC TTC TTA TCA ACA GAG AC - #G AAG AAT CTG TCG GGC2688Gly Ala Leu Thr Ser Phe Leu Ser Thr Glu Th - #r Lys Asn Leu Ser Gly# 895- GTT AGC GGA GTG ACT CTC GGC ACA ATC ATC AT - #G ACT AGC ACT ACG CTT2736Val Ser Gly Val Thr Leu Gly Thr Ile Ile Me - #t Thr Ser Thr Thr Leu# 910- GGG GCG GCG ATG ATC ATT GCA TTG GCG ATC GG - #A TGG AAG CTG GCT CTG2784Gly Ala Ala Met Ile Ile Ala Leu Ala Ile Gl - #y Trp Lys Leu Ala Leu# 925- GTT TGC ATT TCT GTC GTT CCA ATC CTT CTG GC - #A TGC GGC TTC CTC AGA2832Val Cys Ile Ser Val Val Pro Ile Leu Leu Al - #a Cys Gly Phe Leu Arg# 940- TTC TAC ATG CTT GCT CAA TTC CAG CAA CGA TC - #G AAG TCT GCC TAC GAA2880Phe Tyr Met Leu Ala Gln Phe Gln Gln Arg Se - #r Lys Ser Ala Tyr Glu945 9 - #50 9 - #55 9 -#60- GGG TCT GCG AGC TAT GCT TGC GAA GCC ACG TC - #A GCG ATC CGC ACT GTA2928Gly Ser Ala Ser Tyr Ala Cys Glu Ala Thr Se - #r Ala Ile Arg Thr Val# 975- GCA TCA CTC ACT CGC GAA CAA GAT GTC TGG GG - #C GTT TAC CAC GAC CAG2976Ala Ser Leu Thr Arg Glu Gln Asp Val Trp Gl - #y Val Tyr His Asp Gln# 990- CTA CAA AAA CAG GGA CGG AAG AGT TTG ATC TC - #A GTG CTG AGA TCC TCC3024Leu Gln Lys Gln Gly Arg Lys Ser Leu Ile Se - #r Val Leu Arg Ser Ser# 10050- CTG CTG TAT GCC TCG TCG CAG GCA TTG GTG TT - #T TTC TGC GTC GCT TTG3072Leu Leu Tyr Ala Ser Ser Gln Ala Leu Val Ph - #e Phe Cys Val Ala Leu# 10205- GGC TTC TGG TAT GGT GGT ACA CTT CTA GGC CA - #T CAT GAG TAC AGC ATC3120Gly Phe Trp Tyr Gly Gly Thr Leu Leu Gly Hi - #s His Glu Tyr Ser Ile# 10401030 - # 1035- TTC CGC TTC TTC GTC TGC TTT TCT GAG ATT CT - #T TTT GGT GCG CAA TCA3168Phe Arg Phe Phe Val Cys Phe Ser Glu Ile Le - #u Phe Gly Ala Gln Ser# 10550- GCC GGA ACT GTC TTC TCT TTT GCC CCG GAC AT - #G GGT AAG GCA AAG AAT3216Ala Gly Thr Val Phe Ser Phe Ala Pro Asp Me - #t Gly Lys Ala Lys Asn# 10705- GCC GCT GCT CAA TTC AAG AAA CTC TTC GAC AG - #C AAG CCA ACC ATT GAC3264Ala Ala Ala Gln Phe Lys Lys Leu Phe Asp Se - #r Lys Pro Thr Ile Asp# 10850- ATC TGG TCG GAT GAG GGC GAG AAG TTG GAG TC - #T ATG GAA GGC GAA ATC3312Ile Trp Ser Asp Glu Gly Glu Lys Leu Glu Se - #r Met Glu Gly Glu Ile# 11005- GAA TTC CGG GAC GTC CAC TTT AGG TAC CCA AC - #G CGG CCG GAG CAG CCT3360Glu Phe Arg Asp Val His Phe Arg Tyr Pro Th - #r Arg Pro Glu Gln Pro# 11201110 - # 1115- GTT CTT CGA GGA CTG AAT TTG AGC GTG AAG CC - #T GGA CAA TAC ATT GCC3408Val Leu Arg Gly Leu Asn Leu Ser Val Lys Pr - #o Gly Gln Tyr Ile Ala# 11350- CTT GTT GGA CCC AGT GGA TGC GGT AAG AGC AC - #T ACG ATT GCT CTG CTT3456Leu Val Gly Pro Ser Gly Cys Gly Lys Ser Th - #r Thr Ile Ala Leu Leu# 11505- GAG CGA TTT TAT GAC GCA CTT GCT GGA GGG GT - #C TTC GTT GAC GGA AAG3504Glu Arg Phe Tyr Asp Ala Leu Ala Gly Gly Va - #l Phe Val Asp Gly Lys# 11650- GAC ATT ACC AAA CTC AAT GTC AAC TCA TAC CG - #C AGT TTC CTC TCC CTT3552Asp Ile Thr Lys Leu Asn Val Asn Ser Tyr Ar - #g Ser Phe Leu Ser Leu# 11805- GTC AGC CAA GAA CCT ACT CTG TAT CAG GGT AC - #C ATC AAG GAA AAT ATC3600Val Ser Gln Glu Pro Thr Leu Tyr Gln Gly Th - #r Ile Lys Glu Asn Ile# 12001190 - # 1195- CTG CTT GGA GTC GAT AAG GAT GAC GTT TCG GA - #G GAG ACT TTG ATT AAG3648Leu Leu Gly Val Asp Lys Asp Asp Val Ser Gl - #u Glu Thr Leu Ile Lys# 12150- GTC TGC AAA GAT GCC AAC ATC TAT GAT TTC GT - #T ATG TCA CTC CCT GAG3696Val Cys Lys Asp Ala Asn Ile Tyr Asp Phe Va - #l Met Ser Leu Pro Glu# 12305- GGA TTT GAC ACC GTC GTT GGC AGC AAG GGA GG - #C ATG TTG TCT GGT GGA3744Gly Phe Asp Thr Val Val Gly Ser Lys Gly Gl - #y Met Leu Ser Gly Gly# 12450- CAA AAA CAG CGT GTC GCC ATT GCT CGT GCC CT - #C CTG CGT GAC CCC AAG3792Gln Lys Gln Arg Val Ala Ile Ala Arg Ala Le - #u Leu Arg Asp Pro Lys# 12605- GTC CTT CTT CTG GAT GAA GCC ACA TCT GCT CT - #T GAC TCC GAA TCT GAG3840Val Leu Leu Leu Asp Glu Ala Thr Ser Ala Le - #u Asp Ser Glu Ser Glu# 12801270 - # 1275- AAA GTC GTA CAA GCT GCG CTG GAT GCT GCT GC - #C CGC GGG CGG ACA ACG3888Lys Val Val Gln Ala Ala Leu Asp Ala Ala Al - #a Arg Gly Arg Thr Thr# 12950- ATT GCT GTT GCC CAC CGG CTG AGC ACC ATT CA - #A AAC GCT GAT ATA ATT3936Ile Ala Val Ala His Arg Leu Ser Thr Ile Gl - #n Asn Ala Asp Ile Ile# 13105- TAC GTG TTC GAC CAA GGC AAG ATC GTC GAA AG - #T GGA ACG CAC CAC GAG3984Tyr Val Phe Asp Gln Gly Lys Ile Val Glu Se - #r Gly Thr His His Glu# 13250- TTG ATT CGA AAC AAG GGC CGG TAT TAC GAG CT - #G GTC AAT CTG CAG AGT4032Leu Ile Arg Asn Lys Gly Arg Tyr Tyr Glu Le - #u Val Asn Leu Gln Ser# 13405# 4047 ATLeu Gly Lys Thr His1345- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 1349 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:- Met Pro Ala Pro Glu Thr Gly Ala Ser Ser Ar - #g Glu Lys Ser Leu Glu# 15- Asp Leu Gln Val Ala Thr Leu Glu Lys Gly Ar - #g Ser Thr Ser Ser Ser# 30- Gly Ala Asp Asn Glu Lys Pro His Asp His Hi - #s Ser Leu Ser Asp Thr# 45- Ile Met Ala Pro Pro Asp Gly Lys Lys Lys As - #p His Gly Lys Ala Val# 60- Asp Leu Asn Asp Asp Ser Leu Phe Ala His Le - #u Gln Glu His Glu Lys# 80- Glu Val Leu Lys Arg Gln Leu Asp Ala Pro Se - #r Val Lys Val Ser Phe# 95- Phe Thr Leu Tyr Arg Tyr Ala Ser Arg Lys As - #p Ile Leu Ile Ile Leu# 110- Val Ser Ala Ile Cys Ala Ile Ala Ala Gly Al - #a Ala Leu Pro Leu Phe# 125- Thr Ile Leu Phe Gly Ser Leu Ala Ser Ala Ph - #e Gln Gly Ile Ser Leu# 140- Gly Thr Met Pro Tyr His Glu Phe Tyr His Ly - #s Leu Thr Lys Asn Val145 1 - #50 1 - #55 1 -#60- Leu Tyr Phe Val Tyr Leu Gly Ile Ala Glu Ph - #e Val Thr Val Tyr Val# 175- Ser Thr Val Gly Phe Ile Tyr Thr Gly Glu Hi - #s Leu Thr Gln Lys Ile# 190- Arg Glu Asn Tyr Leu Glu Ala Ile Leu Arg Gl - #n Asn Met Ala Tyr Phe# 205- Asp Lys Leu Gly Ala Gly Glu Val Thr Thr Ar - #g Ile Thr Ala Asp Thr# 220- Asn Leu Ile Gln Asp Ala Ile Ser Glu Lys Va - #l Gly Leu Thr Leu Thr225 2 - #30 2 - #35 2 -#40- Ala Phe Ala Thr Phe Val Thr Ala Phe Ile Va - #l Ala Tyr Val Lys Tyr# 255- Trp Lys Leu Ala Leu Ile Cys Thr Ser Thr Il - #e Val Ala Leu Val Met# 270- Val Met Gly Gly Gly Ser Arg Phe Ile Val Ly - #s Tyr Ser Lys Lys Ser# 285- Ile Glu Ser Tyr Gly Ala Gly Gly Thr Val Al - #a Glu Glu Val Ile Ser# 300- Ser Ile Arg Asn Ala Thr Ala Phe Gly Thr Gl - #n Asp Lys Leu Ala Lys305 3 - #10 3 - #15 3 -#20- Gln Tyr Glu Thr His Leu Ala Glu Ala Glu Ly - #s Trp Gly Val Lys Gln# 335- Gln Val Ile Leu Gly Met Met Ile Gly Gly Me - #t Phe Gly Ile Met Phe# 350- Ser Asn Tyr Gly Leu Gly Phe Trp Met Gly Se - #r Arg Phe Val Val Gly# 365- Lys Glu Val Asn Val Gly Gln Val Leu Thr Va - #l Leu Met Ser Ile Leu# 380- Ile Gly Ser Phe Ser Leu Gly Asn Val Ala Pr - #o Asn Gly Gln Ala Phe385 3 - #90 3 - #95 4 -#00- Thr Asn Gly Val Ala Ala Ala Ala Lys Ile Ty - #r Ser Thr Ile Asp Arg# 415- Arg Ser Pro Leu Asp Pro Tyr Ser Asp Glu Gl - #y Lys Val Leu Asp His# 430- Phe Glu Gly Asn Ile Glu Phe Arg Asn Val Ly - #s His Ile Tyr Pro Ser# 445- Arg Pro Glu Val Thr Val Met Glu Asp Val Se - #r Leu Ser Met Pro Ala# 460- Gly Lys Thr Thr Ala Leu Val Gly Pro Ser Gl - #y Ser Gly Lys Ser Thr465 4 - #70 4 - #75 4 -#80- Val Val Gly Leu Val Glu Arg Phe Tyr Leu Pr - #o Val Gly Gly Gln Val# 495- Leu Leu Asp Gly His Asp Ile Gln Thr Leu As - #n Leu Arg Trp Leu Arg# 510- Gln Gln Ile Ser Leu Val Ser Gln Glu Pro Va - #l Leu Phe Ser Thr Thr# 525- Ile Phe Arg Asn Ile Glu His Gly Leu Ile Gl - #y Thr Lys Phe Glu His# 540- Glu Ser Lys Asp Lys Ile Arg Glu Leu Val Gl - #u Asn Ala Ala Arg Met545 5 - #50 5 - #55 5 -#60- Ala Asn Ala His Asp Phe Ile Met Ala Leu Pr - #o Glu Gly Tyr Asp Thr# 575- Asn Val Gly Gln Arg Gly Phe Leu Leu Ser Gl - #y Gly Gln Lys Gln Arg# 590- Ile Ala Ile Ala Arg Ala Ile Val Ser Asp Pr - #o Lys Ile Leu Leu Leu# 605- Asp Glu Ala Thr Ser Ala Leu Asp Thr Lys Se - #r Glu Gly Val Val Gln# 620- Ala Ala Leu Asp Lys Ala Ala Glu Gly Arg Th - #r Thr Ile Val Ile Ala625 6 - #30 6 - #35 6 -#40- His Arg Leu Ser Thr Ile Lys Thr Ala His As - #n Ile Val Ala Met Val# 655- Gly Gly Lys Ile Ala Glu Gln Gly Thr His As - #p Glu Leu Val Asp Arg# 670- Lys Gly Thr Tyr Tyr Lys Leu Val Glu Ala Gl - #n Arg Ile Asn Glu Glu# 685- Lys Glu Ala Glu Ala Leu Glu Ala Asp Ala As - #p Met Asp Ala Asp Asp# 700- Phe Gly Gln Glu Gly Val Thr Arg Ile Lys Th - #r Ala Val Ser Ser Ser705 7 - #10 7 - #15 7 -#20- Asn Ser Leu Asp Ala Val Asp Glu Lys Ala Ar - #g Leu Glu Met Lys Arg# 735- Thr Gly Thr Gln Lys Ser Val Ser Ser Ala Va - #l Leu Ser Lys Lys Val# 750- Pro Glu Gln Phe Glu Lys Tyr Ser Leu Trp Th - #r Leu Val Lys Phe Ile# 765- Gly Ala Phe Asn Arg Pro Glu Leu Gly Tyr Me - #t Leu Ile Gly Leu Thr# 780- Phe Ser Phe Leu Ala Gly Gly Gly Gln Pro Th - #r Gln Ala Phe Leu Tyr785 7 - #90 7 - #95 8 -#00- Ala Lys Ala Ile Ser Thr Leu Ser Leu Pro Gl - #u Ser Met Phe His Lys# 815- Leu Arg His Asp Ala Asn Phe Trp Ser Leu Me - #t Phe Phe Val Val Gly# 830- Ile Ala Gln Phe Ile Ser Leu Ser Ile Asn Gl - #y Thr Ala Phe Ala Ile# 845- Cys Ser Glu Arg Leu Ile Arg Arg Ala Arg Se - #r Gln Ala Phe Arg Ser# 860- Ile Leu Arg Gln Asp Ile Ser Phe Phe Asp Ar - #g Glu Glu Asn Ser Thr865 8 - #70 8 - #75 8 -#80- Gly Ala Leu Thr Ser Phe Leu Ser Thr Glu Th - #r Lys Asn Leu Ser Gly# 895- Val Ser Gly Val Thr Leu Gly Thr Ile Ile Me - #t Thr Ser Thr Thr Leu# 910- Gly Ala Ala Met Ile Ile Ala Leu Ala Ile Gl - #y Trp Lys Leu Ala Leu# 925- Val Cys Ile Ser Val Val Pro Ile Leu Leu Al - #a Cys Gly Phe Leu Arg# 940- Phe Tyr Met Leu Ala Gln Phe Gln Gln Arg Se - #r Lys Ser Ala Tyr Glu945 9 - #50 9 - #55 9 -#60- Gly Ser Ala Ser Tyr Ala Cys Glu Ala Thr Se - #r Ala Ile Arg Thr Val# 975- Ala Ser Leu Thr Arg Glu Gln Asp Val Trp Gl - #y Val Tyr His Asp Gln# 990- Leu Gln Lys Gln Gly Arg Lys Ser Leu Ile Se - #r Val Leu Arg Ser Ser# 10050- Leu Leu Tyr Ala Ser Ser Gln Ala Leu Val Ph - #e Phe Cys Val Ala Leu# 10205- Gly Phe Trp Tyr Gly Gly Thr Leu Leu Gly Hi - #s His Glu Tyr Ser Ile# 10401030 - # 1035- Phe Arg Phe Phe Val Cys Phe Ser Glu Ile Le - #u Phe Gly Ala Gln Ser# 10550- Ala Gly Thr Val Phe Ser Phe Ala Pro Asp Me - #t Gly Lys Ala Lys Asn# 10705- Ala Ala Ala Gln Phe Lys Lys Leu Phe Asp Se - #r Lys Pro Thr Ile Asp# 10850- Ile Trp Ser Asp Glu Gly Glu Lys Leu Glu Se - #r Met Glu Gly Glu Ile# 11005- Glu Phe Arg Asp Val His Phe Arg Tyr Pro Th - #r Arg Pro Glu Gln Pro# 11201110 - # 1115- Val Leu Arg Gly Leu Asn Leu Ser Val Lys Pr - #o Gly Gln Tyr Ile Ala# 11350- Leu Val Gly Pro Ser Gly Cys Gly Lys Ser Th - #r Thr Ile Ala Leu Leu# 11505- Glu Arg Phe Tyr Asp Ala Leu Ala Gly Gly Va - #l Phe Val Asp Gly Lys# 11650- Asp Ile Thr Lys Leu Asn Val Asn Ser Tyr Ar - #g Ser Phe Leu Ser Leu# 11805- Val Ser Gln Glu Pro Thr Leu Tyr Gln Gly Th - #r Ile Lys Glu Asn Ile# 12001190 - # 1195- Leu Leu Gly Val Asp Lys Asp Asp Val Ser Gl - #u Glu Thr Leu Ile Lys# 12150- Val Cys Lys Asp Ala Asn Ile Tyr Asp Phe Va - #l Met Ser Leu Pro Glu# 12305- Gly Phe Asp Thr Val Val Gly Ser Lys Gly Gl - #y Met Leu Ser Gly Gly# 12450- Gln Lys Gln Arg Val Ala Ile Ala Arg Ala Le - #u Leu Arg Asp Pro Lys# 12605- Val Leu Leu Leu Asp Glu Ala Thr Ser Ala Le - #u Asp Ser Glu Ser Glu# 12801270 - # 1275- Lys Val Val Gln Ala Ala Leu Asp Ala Ala Al - #a Arg Gly Arg Thr Thr# 12950- Ile Ala Val Ala His Arg Leu Ser Thr Ile Gl - #n Asn Ala Asp Ile Ile# 13105- Tyr Val Phe Asp Gln Gly Lys Ile Val Glu Se - #r Gly Thr His His Glu# 13250- Leu Ile Arg Asn Lys Gly Arg Tyr Tyr Glu Le - #u Val Asn Leu Gln Ser# 13405- Leu Gly Lys Thr His1345- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 4800 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:- TATAGAAGTG TCCTTTCTAC AAGGGGGAGT AAGACAGGCC CTTACGACAG CA - #TCTCAGAC 60- TACTCTCTTC TACAATCCTC CTTGATTCGC TCGAGTTCCG GAAACCAGAT TG - #TCCGCCAG 120- TTAACCAACT CATGGAGTAG TGCGATTCTG ATTGTGTGAG GATTCCTCAA TC - #TGTGACAT 180- CTTTATCTGA GAGAATCAGT TTTGGCATAC CCTCAACCGC AACATGCCTG CG - #CCTGAAAC 240- CGGCGCCTCC TCTCGGGAGA AGTCCCTCGA GGATTTGCAA GTAGCGACAT TG - #GAGAAAGG 300- ACGTTCCACT TCATCTTCCG GTGCCGACAA TGAAAAGCCA CACGACCATC AT - #TCGTTATC 360- GGACACGATC ATGGCGCCTC CAGATGGCAA GAAAAAGGAT CACGGGAAAG CT - #GTCGACCT 420- GAACGATGAT TCTCTCTTTG CCCATCTCCA GGAGCACGAG AAAGAGGTAC TC - #AAGCGACA 480- GCTTGATGCA CCGTCTGTGA AAGTCTCTTT CTTCACTTTG TATCGCTATG CC - #TCGAGAAA 540- GGACATCCTG ATCATACTCG TGAGCGCAAT CTGTGCTATT GCTGCTGGTG CC - #GCTCTTCC 600- CTTGTTCACA GTATGTATGA CCTGCCTAGC AATGTCCCTA TTTGTCAGTC AT - #TAGAACAA 660- AGAGCTTTTG CAGCTGACGT TTGATCTACT AGATTCTCTT CGGTTCACTA GC - #CTCAGCGT 720- TCCAGGGCAT ATCTCTGGGT ACTATGCCCT ATCATGAGTT CTATCACAAA CT - #GACTAAGA 780- ATGTGCTTTA CTTTGTGTAT CTCGGTATTG CCGAGTTTGT CACAGTCTAT GT - #CAGCACCG 840- TGGGTTTCAT TTATACTGGC GAACATCTCA CACAGAAGAT CCGTGAAAAT TA - #TCTTGAGG 900- CTATCCTGAG GCAGAATATG GCTTACTTCG ACAAGTTGGG CGCCGGTGAA GT - #TACCACGC 960- GTATCACTGC TGATACCAAC CTGATCCAGG ACGCCATCTC TGAGAAAGTT GG - #TCTCACTT1020- TGACCGCATT CGCCACATTT GTAACCGCAT TTATTGTCGC CTACGTCAAG TA - #TTGGAAGT1080- TGGCTCTGAT CTGTACCTCA ACTATCGTCG CGCTGGTCAT GGTTATGGGA GG - #TGGGTCGA1140- GGTTTATTGT GAAGTACAGC AAGAAATCTA TTGAAAGTTA TGGTGCTGGT GG - #AACTGTCG1200- CGGAAGAAGT CATCAGCTCC ATTCGGAATG CTACCGCTTT CGGCACTCAG GA - #TAAGCTCG1260- CCAAGCAATA CGAAACCCAT CTGGCTGAGG CTGAAAAATG GGGCGTCAAA CA - #ACAGGTCA1320- TCCTTGGTAT GATGATTGGT GGTATGTTCG GTATCATGTT CTCGAACTAT GG - #TCTCGGTT1380- TCTGGATGGG ATCTCGCTTC GTTGTCGGTA AAGAAGTCAA CGTGGGCCAA GT - #TCTGACAG1440- TTTTGATGTC TATCCTGATC GGTTCGTTCA GTTTGGGCAA CGTCGCCCCC AA - #TGGTCAGG1500- CCTTTACGAA TGGTGTTGCT GCGGCCGCGA AGATTTACAG CACGATTGAC CG - #CAGATCGC1560- CACTGGACCC CTATTCTGAC GAAGGGAAGG TACTCGACCA TTTTGAAGGA AA - #TATCGAAT1620- TTCGCAATGT CAAACACATC TACCCTTCAA GACCCGAAGT TACAGTCATG GA - #AGATGTCT1680- CTTTATCGAT GCCCGCCGGA AAGACTACCG CATTGGTGGG CCCATCTGGC TC - #TGGAAAGA1740- GTACTGTTGT CGGCTTGGTG GAGCGCTTTT ACCTTCCAGT AGGAGGCCAG GT - #ATTGCTGG1800- ACGGCCATGA TATCCAAACC CTCAACCTCC GTTGGCTGCG ACAGCAGATC TC - #TCTTGTCA1860- GCCAGGAACC TGTTCTTTTC AGCACCACGA TCTTTAGAAA CATCGAACAT GG - #CTTGATTG1920- GCACCAAATT CGAGCATGAG TCGAAGGACA AGATTAGAGA GCTCGTTGAG AA - #TGCGGCCA1980- GAATGGCCAA TGCTCATGAT TTTATTATGG CTCTGCCTGA AGGTTACGAT AC - #GAATGTGG2040- GTCAGCGTGG TTTCTTACTT TCAGGAGGTC AGAAGCAACG TATTGCCATT GC - #TCGTGCCA2100- TTGTCAGTGA CCCCAAGATT CTGTTGCTTG ATGAAGCTAC ATCAGCTTTG GA - #TACCAAGT2160- CCGAGGGCGT CGTCCAAGCC GCTCTTGATA AAGCTGCCGA GGGTAGAACT AC - #CATTGTCA2220- TTGCTCACCG TTTGTCAACA ATCAAAACAG CCCACAACAT TGTTGCCATG GT - #CGGCGGAA2280- AGATTGCCGA ACAGGGAACA CATGACGAAT TGGTCGATCG CAAAGGCACG TA - #CTATAAAC2340- TTGTGGAGGC GCAACGTATC AACGAGGAGA AGGAAGCAGA AGCTCTGGAA GC - #CGACGCCG2400- ACATGGACGC CGATGATTTT GGTCAAGAAG GGGTTACTCG CATCAAGACT GC - #AGTTAGCA2460- GCTCGAATTC TCTCGATGCT GTAGATGAGA AGGCGCGCTT GGAGATGAAG CG - #AACCGGAA2520- CGCAAAAATC GGTTTCGAGT GCCGTTCTAT CTAAGAAAGT CCCCGAGCAG TT - #CGAGAAGT2580- ATTCACTCTG GACCCTCGTC AAGTTCATCG GTGCATTTAA CCGCCCTGAG CT - #TGGTTACA2640- TGCTCATTGG CTTGACTTTC TCGTTCCTTG CCGGTGGTGG TCAACCTACC CA - #GGCTTTTC2700- TGTACGCCAA GGCAATTAGC ACGCTCTCGT TACCCGAATC AATGTTTCAC AA - #ACTCAGGC2760- ATGACGCGAA TTTCTGGTCC TTGATGTTCT TCGTGGTTGG AATTGCTCAA TT - #TATCAGCC2820- TGTCTATCAA TGGTACAGCA TTTGCTATTT GTTCGGAGAG ACTCATTCGC CG - #AGCTAGAA2880- GTCAAGCGTT TAGATCGATT CTTCGTCAGG ACATCTCATT TTTCGACAGG GA - #AGAGAACA2940- GCACCGGTGC CTTGACGTCC TTCTTATCAA CAGAGACGAA GAATCTGTCG GG - #CGTTAGCG3000- GAGTGACTCT CGGCACAATC ATCATGACTA GCACTACGCT TGGGGCGGCG AT - #GATCATTG3060- CATTGGCGAT CGGATGGAAG CTGGCTCTGG TTTGCATTTC TGTCGTTCCA AT - #CCTTCTGG3120- CATGCGGCTT CCTCAGATTC TACATGCTTG CTCAATTCCA GCAACGATCG AA - #GTCTGCCT3180- ACGAAGGGTC TGCGAGCTAT GCTTGCGAAG CCACGTCAGC GATCCGCACT GT - #AGCATCAC3240- TCACTCGCGA ACAAGATGTC TGGGGCGTTT ACCACGACCA GCTACAAAAA CA - #GGGACGGA3300- AGAGTTTGAT CTCAGTGCTG AGATCCTCCC TGCTGTATGC CTCGTCGCAG GC - #ATTGGTGT3360- TTTTCTGCGT CGCTTTGGGC TTCTGGTATG GTGGTACACT TCTAGGCCAT CA - #TGAGTACA3420- GCATCTTCCG CTTCTTCGTC TGCTTTTCTG AGATTCTTTT TGGTGCGCAA TC - #AGCCGGAA3480- CTGTCTTCTC TTTTGCCCCG GACATGGGTA AGGCAAAGAA TGCCGCTGCT CA - #ATTCAAGA3540- AACTCTTCGA CAGCAAGCCA ACCATTGACA TCTGGTCGGA TGAGGGCGAG AA - #GTTGGAGT3600- CTATGGAAGG CGAAATCGAA TTCCGGGACG TCCACTTTAG GTACCCAACG CG - #GCCGGAGC3660- AGCCTGTTCT TCGAGGACTG AATTTGAGCG TGAAGCCTGG ACAATACATT GC - #CCTTGTTG3720- GACCCAGTGG ATGCGGTAAG AGCACTACGA TTGCTCTGCT TGAGCGATTT TA - #TGACGCAC3780- TTGCTGGAGG GGTCTTCGTT GACGGAAAGG ACATTACCAA ACTCAATGTC AA - #CTCATACC3840- GCAGTTTCCT CTCCCTTGTC AGCCAAGAAC CTACTCTGTA TCAGGGTACC AT - #CAAGGAAA3900- ATATCCTGCT TGGAGTCGAT AAGGATGACG TTTCGGAGGA GACTTTGATT AA - #GGTCTGCA3960- AAGATGCCAA CATCTATGAT TTCGTTATGT CACTCCCGTA AGTTTACTGC CT - #CGCTGACT4020- CCTTTCATGC CTGGCGGTTC TGCTAACATG CTACAACAGT GAGGGATTTG AC - #ACCGTCGT4080- TGGCAGCAAG GGAGGCATGT TGTCTGGTGG ACAAAAACAG CGTGTCGCCA TT - #GCTCGTGC4140- CCTCCTGCGT GACCCCAAGG TCCTTCTTCT GGATGAAGCC ACATCTGCTC TT - #GACTCCGA4200- ATCTGAGAAA GTCGTACAAG CTGCGCTGGA TGCTGCTGCC CGCGGGCGGA CA - #ACGATTGC4260- TGTTGCCCAC CGGCTGAGCA CCATTCAAAA CGCTGATATA ATTTACGTGT TC - #GACCAAGG4320- CAAGATCGTC GAAAGTGGAA CGCACCACGA GTTGATTCGA AACAAGGGCC GG - #TATTACGA4380- GCTGGTCAAT CTGCAGAGTC TCGGAAAGAC TCATTGATCA TTCCTTCCCC CT - #TCTTCTCA4440- TGCTGTACCA ATGTACCAAT CTTCTTAATA TCTTCCTCCT CCCTGCTCAA TC - #ATGTCATT4500- CTTGGTGCTG AAAATACTGT GGATATACCA CCCCGCTTAT GTGTCTATGA TT - #CCCCTATA4560- AAATTTTCAG CTTAATTGTC CTCGTCTTTG TACCTTATCC TCATCTTCGT TA - #CTTAAAGC4620- GCCGTATTTT TGGGCTGTCA TTGGAGTTGA TGGGTATCAC TTCTACTTGG GT - #GGGCGATA4680- GGACAGAATC TTGCATCGCA GTCTTTTGCT AAGTGAACAC GATTTCAAAT TT - #ATCATGTT4740- CTATATAATT CGACGCATAT CCACATAGGG GGAACGAAGA ACAAGATGCA TC - #ACAAACAG4800- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 21 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:#21 GCCA G- (2) INFORMATION FOR SEQ ID NO:5:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 21 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:#21 TGAT G- (2) INFORMATION FOR SEQ ID NO:6:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 28 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:# 28 TGCC TGCGCCTG- (2) INFORMATION FOR SEQ ID NO:7:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 21 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:#21 CTTT C- (2) INFORMATION FOR SEQ ID NO:8:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 34 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:# 34 CAGA CTACGCTTGA TAAT- (2) INFORMATION FOR SEQ ID NO:9:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:# 36 AGTC TGGGACGTCG TATGGG__________________________________________________________________________

Number	Name	Date
4912039	Riordan	Mar 1990
5489519	Deeley et al.	Feb 1996
5516655	Peery et al.	May 1996

Multiple drug resistance gene of Aspergillus fumigatus

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Non-Patent Literature Citations (16)

Entry
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