Modified factor VIII

Abstract

The invention relates to a modified B-domainless form of porcine factor VIII, to a DNA encoding the same, and to the use thereof for treatment of hemophilia.

Description

BACKGROUND OF THE INVENTION

Blood clotting begins when platelets adhere to the cut wall of an injured blood vessel at a lesion site. Subsequently, in a cascade of enzymatically regulated reactions, soluble fibrinogen molecules are converted by the enzyme thrombin to insoluble strands of fibrin that hold the platelets together in a thrombus. At each step in the cascade>a protein precursor is converted to a protease that cleaves the next protein precursor in the series. Cofactors are required at most of the steps.

Factor VIII circulates as an inactive precursor in blood, bound tightly and non-covalently to von Willebrand factor. Factor VIII is proteolytically activated by thrombin or factor Xa, which dissociates it from von Willebrand factor and activates its procoagulant function in the cascade. In its active form, the protein factor VIIIa is a cofactor that increases the catalytic efficiency of factor IXa toward factor X activation by several orders of magnitude.

People with deficiencies in factor VIII or antibodies against factor VIII who are not treated with factor VIII suffer uncontrolled internal bleeding that may cause a range of serious symptoms, from inflammatory reactions in joints to early death. Severe hemophiliacs, who number about 10,000 in the United States, can be treated with infusion of human factor VIII, which will restore the blood's normal clotting ability if administered with sufficient frequency and concentration. The classic definition of factor VIII, in fact, is that substance present in normal blood plasma that corrects the clotting defect in plasma derived from individuals with hemophilia A.

The development of antibodies (“inhibitors” or “inhibitory antibodies”) that inhibit the activity of factor VIII is a serious complication in the management of patients with hemophilia. Autoantibodies develop in approximately 20% of patients with hemophilia A in response to therapeutic infusions of factor VIII. In previously untreated patients with hemophilia A who develop inhibitors, the inhibitor usually develops within one year of treatment. Additionally, autoantibodies that inactivate factor VIII occasionally develop in individuals with previously normal factor VIII levels. If the inhibitor titer is low enough, patients can be managed by increasing the dose of factor VIII. However, often the inhibitor titer is so high that it cannot be overwhelmed by factor VIII. An alternative strategy is to bypass the need for factor VIII during normal hemostasis using factor IX complex preparations (for example, KONYNE®, Proplex®) or recombinant human factor VIIa. Additionally, since porcine factor VIII usually has substantially less reactivity with inhibitors than human factor VIII, a partially purified porcine factor VIII preparation (HYATE:C®) has been used. Many patients who have developed inhibitory antibodies to human factor VIII have been successfully treated with porcine factor VIII and have tolerated such treatment for long periods of time. However, administration of porcine factor VIII is not a complete solution because inhibitors may develop to porcine factor VIII after one or more infusions in some patients.

Several preparations of human plasma-derived factor VIII of varying degrees of purity are available commercially for the treatment of hemophilia A. These include a partially-purified factor VIII derived from the pooled blood of many donors that is heat- and detergent-treated for viruses but contain a significant level of antigenic proteins; a monoclonal antibody-purified factor VIII that has lower levels of antigenic impurities and viral contamination; and recombinant human factor VIII, clinical trials for which are underway. Unfortunately, human factor VIII is unstable at physiologic concentrations and pH, is present in blood at an extremely low concentration (0.2 μg/ml plasma), and has low specific clotting activity. Public health concerns regarding the risk of viruses or other blood-borne contaminants have limited the usefulness of porcine factor VIII purified from porcine blood.

Hemophiliacs require daily replacement of factor VIII to prevent bleeding and the resulting deforming hemophilic arthropathy. However, supplies have been inadequate and problems in therapeutic use occur due to difficulty in isolation and purification, immunogenicity, and the necessity of removing the AIDS and hepatitis infectivity risk. The use of recombinant human factor VIII or partially-purified porcine factor VIII will not resolve all the problems.

The problems associated with the commonly used, commercially available, plasma-derived factor VIII have stimulated significant interest in the development of a better factor VIII product. There is a need for a more potent factor VIII molecule so that more units of clotting activity can be delivered per molecule; a factor VIII molecule that is stable at a selected pH and physiologic concentration; a factor VIII molecule that is less apt to cause production of inhibitory antibodies; and a factor VIII molecule that evades immune detection in patients who have already acquired antibodies to human factor VIII.

It is therefore an object of the present invention to provide a factor VIII that corrects hemophilia in a patient deficient in factor VIII or having inhibitors to human factor VIII.

It is a further object of the present invention to provide methods for treatment of hemophiliacs.

It is still another object of the present invention to provide a factor VIII that is stable at a selected pH and physiologic concentration.

It is yet another object of the present invention to provide a factor VIII that has greater coagulant activity than human factor VIII.

It is an additional object of the present invention to provide a factor VIII against which less antibody is produced.

It is a further object of the invention to provide a method for making recombinant porcine factor VIII and specifically modified porcine factor VIII.

SUMMARY OF THE INVENTION

The determination of the entire DNA sequence encoding porcine factor VIII set forth herein has enabled, for the first time, the synthesis of full-length porcine factor VIII by expressing the DNA encoding porcine factor VIII in a suitable host cell. Purified recombinant porcine factor VIII is therefore an aspect of the present invention. The DNA encoding each domain of porcine factor VIII as well as any specified fragment thereof, can be similarly expressed. Furthermore, porcine fVIII having all or part of the B domain deleted (B-domainless porcine fVIII) is made available as part of the present invention, by expression DNA encoding porcine fVIII having a deletion of one or more codons of the B-domain.

Also provided are pharmaceutical compositions and methods for treating patients having factor VIII deficiency comprising administering recombinant porcine factor VIII or a modified recombinant porcine factor VIII, in particular a B-domainless porcine factor VIII.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-1H taken together provide an aligned sequence comparison of the human, pig and mouse factor VIII acid sequences.

DETAILED DESCRIPTION OF THE INVENTION

Unless otherwise specified or indicated, as used herein, “factor VIII” denotes any functional factor VIII protein molecule from any mammal.

As used herein, “mammalian factor VIII” includes factor VIII with amino acid sequence derived from any non-human mammal, unless otherwise specified. “Animal”, as used herein, refers to pig and other non-human mammals.

A “fusion protein” or “fusion factor VIII or fragment thereof”, as used herein, is the product of a hybrid gene in which the coding sequence for one protein is altered, for example, by joining part of it to the coding sequence for a second protein from a different gene in proper reading frame register such that uninterrupted transcription and translation of the joined segments can occur to produce a hybrid gene that encodes the fusion protein.

A “corresponding” nucleic acid or amino acid or sequence of either, as used herein, is one present at a site in a factor VIII molecule or fragment thereof that has the same structure and/or function as a site in the factor VIII molecule of another species, although the nucleic acid or amino acid number may not be identical. A DNA sequence “corresponding to” another factor VIII sequence substantially corresponds to such sequence, and hybridizes to the sequence of the designated SEQ ID NO. under stringent conditions. A DNA sequence “corresponding to” another factor VIII sequence also includes a sequence that results in the expression of a factor VIII or fragment thereof and would hybridize to the designated SEQ ID NO. but for the redundancy of the genetic code.

A “unique” amino acid residue or sequence, as used herein, refers to an amino acid sequence or residue in the factor VIII molecule of one species that is different from the homologous residue or sequence in the factor VIII molecule of another species.

“Specific activity,” as used herein, refers to the activity that will correct the coagulation defect of human factor VIII deficient plasma. Specific activity is measured in units of clotting activity per milligram total factor VIII protein in a standard assay in which the clotting time of human factor VIII deficient plasma is compared to that of normal human plasma. One unit of factor VIII activity is the activity present in one milliliter of normal human plasma. In the assay, the shorter the time for clot formation, the greater the activity of the factor VIII being assayed. Porcine factor VIII has coagulation activity in a human factor VIII assay.

“Expression” refers to the set of processes that occur whereby genetic information is utilized to yield a product. A DNA encoding the amino acid sequence of porcine factor VIII can be “expressed” within a mammalian host cell to yield porcine factor VIII protein. The materials, genetic structures, host cells and conditions which permit expression of a given DNA sequence to occur are well-known in the art and can be manipulated to affect the time and amount of expression, as well as the intra- or extra-cellular location of the expressed protein. For example, by including DNA encoding a signal peptide at the 5′ end of the DNA encoding porcine factor VIII (the 5′ end being, by convention, that end encoding the NH 2 terminus of the protein) the expressed protein becomes exported from the interior of the host cell into the culture medium. Providing a signal peptide coding DNA in combination with the porcine factor VIII coding DNA is advantageous because the expressed factor VIII is exported into the culture medium which simplifies the process of purification. A preferred signal peptide is a mammalian factor VIII signal peptide.

The human factor VIII cDNA nucleotide and predicted amino acid sequences are shown in SEQ ID NOs:1 and 2, respectively. Factor VIII is synthesized as an approximately 300 kDa single chain protein with internal sequence homology that defines the “domain” sequence NH 2 -A1-A2-B-A3-C1-C2-COOH. In a factor VIII molecule, a “domain”, as used herein, is a continuous sequence of amino acids that is defined by internal amino acid sequence identity and sites of proteolytic cleavage by thrombin. Unless otherwise specified, factor VIII domains include the following amino acid residues, when the sequences are aligned with the human amino acid sequence (SEQ ID NO:2): A1, residues Ala1-Arg372; A2, residues Ser373-Arg740; B, residues Ser741-Arg1648; A3, residues Ser1690-Ile2032; C1, residues Arg2033-Asn2172; C2, residues Ser2173-Tyr2332. The A3-C1-C2 sequence includes residues Ser1690-Tyr2332. The remaining segment, residues Glu1649-Arg1689, is usually referred to as the factor VIII light chain activation peptide. Factor VIII is proteolytically activated by thrombin or factor Xa, which dissociates it from von Willebrand factor, forming factor VIIIa, which has procoagulant function. The biological function of factor VIIIa is to increase the catalytic efficiency of factor IXa toward factor X activation by several orders of magnitude. Thrombin-activated factor VIIIa is a 160 kDa A1/A2/A3-C1-C2 heterotrimer that forms a complex with factor IXa and factor X on the surface of platelets or monocytes. A “partial domain” as used herein is a continuous sequence of amino acids forming part of a domain.

“Subunits” of human or animal factor VIII, as used herein, are the heavy and light chains of the protein. The heavy chain of factor VIII contains three domains, A1, A2, and B. The light chain of factor VIII also contains three domains, A3, C1, and C2.

The terms “epitope,” “antigenic site,” and “antigenic determinant,” as used herein, are used synonymously and are defined as a portion of the human, or animal factor VIII or fragment thereof that is specifically recognized by an antibody. It can consist of any number of amino acid residues, and it can be dependent upon the primary, secondary, or tertiary structure of the protein.

The term “immunogenic site,” as used herein, is defined as a region of the human or animal factor VIII, or fragment thereof, that specifically elicits the production of antibody to the factor VIII, or fragment, in a human or animal, as measured by routine protocols, such as immunoassay, e.g. ELISA, or the Bethesda assay, described herein. It can consist of any number of amino acid residues, and it can be dependent upon the primary, secondary, or tertiary structure of the protein. In some embodiments, the hybrid or hybrid equivalent factor VIII or fragment thereof is nonimmunogenic or less immunogenic in an animal or human than human or porcine factor VIII.

“Factor VIII deficiency,” as used herein, includes deficiency in clotting activity caused by production of defective factor VIII, by inadequate or no production of factor VIII, or by partial or total inhibition of factor VIII by inhibitors. Hemophilia A is a type of factor VIII deficiency resulting from a defect in an X-linked gene and the absence or deficiency of the factor VIII protein it encodes.

As used herein, “diagnostic assays” include assays that in some manner utilize the antigen-antibody interaction to detect and/or quantify the amount of a particular antibody that is present in a test sample to assist in the selection of medical therapies. There are many such assays known to those of skill in the art. As used herein, human, porcine or modified porcine factor VIII DNA or fragment thereof and protein expressed therefrom, in whole or in part, can be substituted for the corresponding reagents in the otherwise known assays, whereby the modified assays may be used to detect and/or quantify antibodies to factor VIII. It is the use of these reagents, the factor VIII DNA or fragment thereof or protein expressed therefrom, that permits modification of known assays for detection of antibodies to human or animal factor VIII. Such assays include, but are not limited to ELISAs, immunodiffusion assays, and immunoblots. Suitable methods for practicing any of these assays are known to those of skill in the art. As used herein, the factor VIII or fragment thereof that includes at least one epitope of the protein can be used as the diagnostic reagent. Examples of other assays in which human, porcine or modified porcine factor VIII or fragment thereof can be used include the Bethesda assay and anticoagulation assays.

The term “DNA encoding a protein, such as porcine factor VIII” means a polydeoxynucleic acid whose nucleotide sequence embodies coding information to a host cell for the amino acid sequence of the protein, e.g. porcine factor VIII, according to the known relationships of the genetic code.

The “expression product” of a DNA encoding a human or animal factor VIII or a modified factor VIII is the product obtained from expression of the referenced DNA in a suitable host cell, including such features of pre- or post-translational modification of protein encoded by the referenced DNA, including but not limited to glycosylation, proteolytic cleavage and the like. It is known in the art that such modifications can occur and can differ somewhat depending upon host cell type and other factors, and can result in molecular isoforms of the product, with retention of procoagulant activity. See, e.g. Lind, P. et al., Eur. J. Biochem . 232:1927 (1995), incorporated herein by reference.

An “expression vector” is a DNA element, often of circular structure, having the ability to replicate autonomously in a desired host cell, or to integrate into a host cell genome and also possessing certain well-known features which permit expression of a coding DNA inserted into the vector sequence at the proper site and in proper orientation. Such features can include, but are not limited to, one or more promoter sequences to direct transcription initiation of the coding DNA and other DNA elements such as enhancers, polyadenylation sites and the like, all as well known in the art. The term “expression vector” is used to denote both a vector having a DNA coding sequence to be expressed inserted within its sequence, and a vector having the requisite expression control elements so arranged with respect to an insertion site that it can serve to express any coding DNA inserted into the site, all as well-known in the art. Thus, for example, a vector lacking a promoter can become an expression vector by the insertion of a promoter combined with a coding DNA.

GENERAL DESCRIPTION OF METHODS

U.S. Pat. No. 5,364,771 described the discovery of hybrid human/porcine factor VIII molecules having coagulant activity, in which elements of the factor VIII molecule of human or pig are substituted for corresponding elements of the factor VIII molecule of the other species. U.S. Pat. No. 5,663,060 describes procoagulant hybrid human/animal and hybrid equivalent factor VIII molecules, in which elements of the factor VIII molecule of one species are substituted for corresponding elements of the factor VIII molecule of the other species.

Since current information indicates that the B domain has no inhibitory epitope and has no known effect on factor VIII function, in some embodiments the B domain is wholly or partially deleted in the active hybrid or hybrid equivalent factor VIII molecules or fragments thereof (“B(−) factor VIII”) prepared by any of the methods described herein.

The human factor VIII gene was isolated and expressed in mammalian cells, as reported by Toole, J. J. et al. (1984) Nature 312:342-347 (Genetics Institute); Gitschier, J. et al.(1984) Nature 312:326-330 (Genentech); Wood, W. I. et al. (1984) Nature 312:330-337 (Genentech); Vehar, G. A. et al. (1984) Nature 312:337-342 (Genentech); WO 87/04187; WO 88/08035; WO 88/03558; U.S. Pat. No. 4,757,006, and the amino acid sequence was deduced from cDNA. U.S. Pat. No. 4,965,199 to Capon et al. discloses a recombinant DNA method for producing factor VIII in mammalian host cells and purification of human factor VIII. Human factor VIII expression on CHO (Chinese hamster ovary) cells and BHKC (baby hamster kidney cells) has been reported. Human factor VIII has been modified to delete part or all of the B domain (U.S. Pat. No. 4,868,112), and replacement of the human factor VIII B domain with the human factor V B domain has been attempted (U.S. Pat. No. 5,004,803). The cDNA sequence encoding human factor VIII and predicted amino acid sequence are shown in SEQ ID NOs:1 and 2, respectively. In SEQ ID NO:1, the coding region begins at nucleotide position 208, the triplet GCC being the codon for amino acid number 1 (Ala) of the mature protein as given in SEQ ID NO:2.

Porcine factor VIII has been isolated from plasma [Fass, D. N. et al. (1982) Blood 59:594]. Partial amino acid sequence of porcine factor VIII corresponding to portions of the N-terminal light chain sequence having homology to ceruloplasmin and coagulation factor V were described by Church et al. (1984) Proc. Natl. Acad. Sci. USA 81:6934. Toole, J. J. et al. (1984) Nature 312:342-347 described the partial sequencing of the N-terminal end of four amino acid fragments of porcine factor VIII but did not characterize the fragments as to their positions in the factor VIII molecule. The amino acid sequence of the B and part of the A2 domains of porcine factor VIII were reported by Toole, J. J. et al. (1986) Proc. Natl. Acad. Sci, USA 83:5939-5942. The cDNA sequence encoding the complete A2 domain of porcine factor VIII and predicted amino acid sequence and hybrid human/porcine factor VIII having substitutions of all domains, all subunits, and specific amino acid sequences were disclosed in U.S. Pat. No. 5,364,771 entitled “Hybrid Human/Porcine factor VIII” issued on Nov. 15, 1994, and in WO 93/20093 published Oct. 14, 1993. The cDNA sequence encoding the A2 domain of porcine factor VIII corresponding to residues 373-740 in mature human factor VIII, as shown in SEQ ID NO:1, and the predicted amino acid sequence are shown in SEQ ID NOs:3 and 4, respectively. More recently, the nucleotide and corresponding amino acid sequences of part of the A1 domain lacking the first 198 amino acid and of the A2 domain of porcine factor VIII were reported in WO 94/11503, published May 26, 1994. The entire nucleotide sequence encoding porcine factor VIII, including the complete A1 domain, activation peptide, A3, C1 and C2 domains, as well as the encoded amino acid sequence, was finally obtained by Lollar, as disclosed in U.S. Pat. No. 5,859,204, issued Jan. 12, 1999, and in WO 97/49725, published Dec. 31, 1997, both incorporated herein by reference.

Both porcine and human factor VIII are isolated from plasma as a two subunit protein. The subunits, known as the heavy chain and light chain, are held together by a non-covalent bond that requires calcium or other divalent metal ions. The heavy chain of factor VIII contains three domains, A1, A2, and B, which are linked covalently. The light chain of factor VIII also contains three domains, designated A3, C1, and C2. The B domain has no known biological function and can be removed, or partially removed from the molecule proteolytically or by recombinant DNA technology methods without significant alteration in any measurable parameter of factor VIII. Human recombinant factor VIII has a similar structure and function to plasma-derived factor VIII, though it is not glycosylated unless expressed in mammalian cells.

Both human and porcine activated factor VIII (“factor VIIIa”) have three subunits due to cleavage of the heavy chain between the A1 and A2 domains. This structure is designated A1/A2/A3-C1-C2. Human factor Villa is not stable under the conditions that stabilize porcine factor VIIIa, presumably because of the weaker association of the A2 subunit of human factor VIIIa. Dissociation of the A2 subunit of human and porcine factor VIIIa is associated with loss of activity in the factor VIIIa molecule. Yakhyaev, A. et al. (1997) Blood 90:Suppl. 1, Abstract #126, reported binding of A2 domain by low density lipoprotein receptor-related protein, suggesting that cellular uptake of A2 mediated by such binding acts to down-regulate factor VIII activity.

Expression of “B-domainless factor VIII” is enhanced by including portions of the B-domain. The inclusion of those parts of the B domain designated “SQ” [Lind, P. et al. (1995) supra] was reported to result in favorable expression. “SQ” constructs lack all of the human B domain except for 5 amino acids of the B domain N-terminus and 9 amino acids of the B domain C-terminus.

The purified hybrid factor VIII or fragment thereof can be assayed for immunoreactivity and coagulation activity by standard assays including, for example, the plasma-free factor VIII assay, the one-stage clotting assay, and the enzyme-linked immunosorbent assay using purified recombinant human factor VIII as a standard.

Other vectors, including both plasmid and eukaryotic viral vectors, may be used to express a recombinant gene construct in eukaryotic cells depending on the preference and judgment of the skilled practitioner (see, for example, Sambrook et al., Chapter 16). Other vectors and expression systems, including bacterial, yeast, and insect cell systems, can be used but are not preferred due to differences in, or lack of, glycosylation.

Recombinant factor VIII protein can be expressed in a variety of cells commonly used for culture and recombinant mammalian protein expression. In particular, a number of rodent cell lines have been found to be especially useful hosts for expression of large proteins. Preferred cell lines, available from the American Type Culture Collection, Rockville, Md., include baby hamster kidney cells, and chinese hamster ovary (CHO) cells which are cultured using routine procedures and media.

The basis for the greater coagulant activity of porcine factor VIII appears to be the more rapid spontaneous dissociation of the human A2 subunit from human factor VIIIa than the porcine A2 subunit from porcine factor VIIIa. Dissociation of the A2 subunit leads to loss of activity, [Lollar, P. et al. (1990) J. Biol. Chem . 265:1688-1692; Lollar, P. et al. (1992) J. Biol. Chem . 267:23652-23657; Fay, P. J. et al. (1992) J. Biol. Chem . 267:13246-13250].

Factor VIII Molecules with Reduced Immunoreactivity:

Epitopes that are immunoreactive with antibodies that inhibit the coagulant activity of factor VIII (“inhibitors” or “inhibitory antibodies”) have been characterized based on known structure-function relationships in factor VIII. Presumably, inhibitors could act by disrupting any of the macromolecular interactions associated with the domain structure of factor VIII or its associations with von Willebrand factor, thrombin, factor Xa, factor IXa, or factor X. However, most inhibitory antibodies to human factor VIII act by binding to epitopes located in the 40 kDa A2 domain or 20 kDa C2 domain of factor VIII, disrupting specific functions associated with these domains, as described by Fulcher et al. (1985) Proc. Natl. Acad. Sci USA 82:7728-7732; and Scandella et al. (1988) Proc. Natl. Acad. Sci. USA 85:6152-6156. In addition to the A2 and C2 epitopes, there may be a third epitope in the A3 or C1 domain of the light chain of factor VIII, according to Scandella et al. (1993) Blood 82:1767-1775. The significance of this putative third epitope is unknown, but it appears to account for a minor fraction of the epitope reactivity in factor VIII.

Anti-A2 antibodies block factor X activation, as shown by Lollar et al. (1994) J. Clin. Invest . 93:2497-2504. Previous mapping studies by deletion mutagenesis described by Ware et al. (1992) Blood Coagul. Fibrinolysis 3:703-716, located the A2 epitope to within a 20 kDa region of the NH 2 -terminal end of the 40 kDa A2 domain. Competition immunoradiometric assays have indicated that A2 inhibitors recognize either a common epitope or narrowly clustered epitopes, as described by Scandella et al. (1992) Throm. Haemostas 67:665-671, and as demonstrated in U.S. Pat. No. 5,859,204.

Animal or modified animal factor VIII molecules can be tested in humans for their reduced antigenicity and/or immunogenicity in clinical trials. In one type of trial, designed to determine whether the factor VIII is immunoreactive with inhibitory antibodies, factor VIII is administered, preferably by intravenous infusion, to approximately 25 patients having factor VIII deficiency who have antibodies that inhibit the coagulant activity of therapeutic human factor VIII. The dosage of the animal or modified animal factor VIII is in a range between 5 and 50 Units/kg body weight, preferably 10-50 Units/kg, and most preferably 40 Units/kg body weight. Approximately 1 hour after each administration, the recovery of factor VIII from blood samples is measured in a one-stage coagulation assay. Samples are taken again approximately 5 hours after infusion, and recovery is measured. Total recovery and the rate of disappearance of factor VIII from the samples is predictive of the antibody titer and inhibitory activity. If the antibody titer is high, factor VIII recovery usually cannot be measured. The recovery results are compared to the recovery results in patients treated with plasma-derived human factor VIII, recombinant human factor VIII, plasma-derived porcine factor VIII, and other commonly used therapeutic forms of factor VIII or factor VIII substitutes.

After identification of clinically significant epitopes, recombinant factor VIII molecules can be expressed that have less than or equal cross-reactivity compared with plasma-derived porcine factor VIII when tested in vitro against a broad survey of inhibitor plasmas. Additional mutagenesis in epitopic regions can be done to reduce cross-reactivity. Reduced cross-reactivity, although desirable, is not necessary to produce a product that may have advantages over the existing plasma-derived porcine factor VIII concentrate, which can produce side effects due to contaminant porcine proteins or contaminant infectious agents such as viruses or prions. A recombinant porcine or modified porcine factor VIII molecule will not contain foreign porcine proteins.

Diagnostic Assays.

The factor VIII cDNA and/or protein expressed therefrom, in whole or in part, can be used in assays as diagnostic reagents for the detection of inhibitory antibodies to human or animal factor VIII or modified animal VIII in substrates, including, for example, samples of serum and body fluids of human patients with factor VIII deficiency. These antibody assays include assays such as ELISA assays, immunoblots, radioimmunoassays, immunodiffusion assays, and assay of factor VIII biological activity (e.g., by coagulation assay). Techniques for preparing these reagents and methods for use thereof are known to those skilled in the art. For example, an immunoassay for detection of inhibitory antibodies in a patient serum sample can include reacting the test sample with a sufficient amount of the factor VIII to be tested that a detectable complex can be formed with the inhibitory antibodies in the sample of the test factor VIII is indeed antigenic.

Nucleic acid and amino acid probes can be prepared based on the sequence of the hybrid factor VIII cDNA or protein molecule or fragments thereof. In some embodiments, these can be labeled using dyes or enzymatic, fluorescent, chemiluminescent, or radioactive labels that are commercially available. The amino acid probes can be used, for example, to screen sera or other body fluids where the presence of inhibitors to human, animal, or hybrid human/animal factor VIII is suspected. Levels of inhibitors can be quantitated in patients and compared to healthy controls, and can be used, for example, to determine whether a patient with a factor VIII deficiency can be treated with an animal or modified animal factor VIII. The cDNA probes can be used, for example, for research purposes in screening DNA libraries.

Pharmaceutical Compositions.

Pharmaceutical compositions containing recombinant porcine or modified porcine factor VIII, alone or in combination with appropriate pharmaceutical stabilization compounds, delivery vehicles, and/or carrier vehicles, are prepared according to known methods, as described in Remington's Pharmaceutical Sciences by E. W. Martin.

In one preferred embodiment, the preferred carriers or delivery vehicles for intravenous infusion are physiological saline or phosphate buffered saline.

In another preferred embodiment, suitable stabilization compounds, delivery vehicles, and carrier vehicles include but are not limited to other human or animal proteins such as albumin.

Phospholipid vesicles or liposomal suspensions are also preferred as pharmaceutically acceptable carriers or delivery vehicles. These can be prepared according to methods known to those skilled in the art and can contain, for example, phosphatidylserine/-phosphatidylcholine or other compositions of phospholipids or detergents that together impart a negative charge to the surface, since factor VIII binds to negatively charged phospholipid membranes. Liposomes may be prepared by dissolving appropriate lipid(s) (such as stearoyl phosphatidyl ethanolamine, stearoyl phosphatidyl choline, arachadoyl phosphatidyl choline, and cholesterol) in an inorganic solvent that is then evaporated, leaving behind a thin film of dried lipid on the surface of the container. An aqueous solution of the hybrid factor VIII is then introduced into the container. The container is then swirled by hand to free lipid material from the sides of the container and to disperse lipid aggregates, thereby forming the liposomal suspension.

The recombinant porcine or modified porcine factor VIII can be combined with other suitable stabilization compounds, delivery vehicles, and/or carrier vehicles, including vitamin K dependent clotting factors, tissue factor, and von Willebrand factor (vWf) or a fragment of vWf that contains the factor VIII binding site, and polysaccharides such as sucrose.

Recombinant porcine or modified porcine factor VIII can also be delivered by gene therapy in the same way that human factor VIII can be delivered, using delivery means such as retroviral vectors. This method consists of incorporation of the desired factor VIII construct cDNA into human cells that are transplanted directly into a factor VIII deficient patient or that are placed in an implantable device, permeable to the factor VIII molecules but impermeable to cells, that is then transplanted. The preferred method will be retroviral-mediated gene transfer. In this method, an exogenous gene (e.g., a factor VIII cDNA) is cloned into the genome of a modified retrovirus. The gene is inserted into the genome of the host cell by viral machinery where it will be expressed by the cell. The retroviral vector is modified so that it will not produce virus, preventing viral infection of the host. The general principles for this type of therapy are known to those skilled in the art and have been reviewed in the literature [e.g., Kohn, D. B. et al. (1989) Transufusion 29:812-820].

Porcine or modified porcine factor VIII can be stored bound to vWf to increase the half-life and shelf-life of the hybrid molecule. Additionally, lyophilization of factor VIII can improve the yields of active molecules in the presence of vWf. Current methods for storage of human and animal factor VIII used by commercial suppliers can be employed for storage of recombinant factor VIII. These methods include: (1) lyophilization of factor VIII in a partially-purified state (as a factor VIII “concentrate” that is infused without further purification); (2) immunoaffinity-purification of factor VIII by the Zimmerman method and lyophilization in the presence of albumin, which stabilizes the factor VIII; (3) lyophilization of recombinant factor VIII in the presence of albumin.

Additionally, porcine or modified porcine factor VIII has been found to be indefinitely stable at 4° C. in 0.6 M NaCl, 20 mM MES, and 5 mM CaCl 2 at pH 6.0 and also can be stored frozen in these buffers and thawed with minimal loss of activity.

Methods of Treatment.

Recombinant porcine or modified porcine factor VIII is used to treat uncontrolled bleeding due to factor VIII deficiency (e.g., intraarticular, intracranial, or gastrointestinal hemorrhage) in hemophiliacs with and without inhibitory antibodies and in patients with acquired factor VIII deficiency due to the development of inhibitory antibodies. The active materials are preferably administered intravenously.

Additionally, recombinant porcine or modified porcine factor VIII can be administered by transplant of cells genetically engineered to produce the protein by implantation of a device containing such cells, as described above.

In a preferred embodiment, pharmaceutical compositions of recombinant porcine or modified porcine factor VIII alone or in combination with stabilizers, delivery vehicles, and/or carriers are infused into patients intravenously according to the same procedure that is used for infusion of human or animal factor VIII.

The treatment dosages of recombinant porcine or modified porcine factor VIII composition that must be administered to a patient in need of such treatment will vary depending on the severity of the factor VIII deficiency. Generally, dosage level is adjusted in frequency, duration, and units in keeping with the severity and duration of each patient's bleeding episode. Accordingly, the factor VIII is included in a pharmaceutically acceptable carrier, delivery vehicle, or stabilizer in an amount sufficient to deliver to a patient a therapeutically effective amount of the protein to stop bleeding, as measured by standard clotting assays.

Factor VIII is classically defined as that substance present in normal blood plasma that corrects the clotting defect in plasma derived from individuals with hemophilia A. The coagulant activity in vitro of purified and partially-purified forms of factor VIII is used to calculate the dose of factor VIII for infusions in human patients and is a reliable indicator of activity recovered from patient plasma and of correction of the in vivo bleeding defect. There are no reported discrepancies between standard assay of novel factor VIII molecules in vitro and their behavior in the dog infusion model or in human patients, according to Lusher, J. M. et al. 328 New Engl. J. Med . 328:453-459; Pittman, D. D. et al. (1992) Blood 79:389-397; and Brinkhous et al. (1985) Proc. Natl. Acad. Sci . 82:8752-8755.

Usually, the desired plasma factor VIII activity level to be achieved in the patient through administration of the recombinant porcine or modified porcine factor VIII is in the range of 30-100% of normal. In a preferred mode of administration of the therapeutic factor VIII, the composition is given intravenously at a preferred dosage in the range from about 5 to 50 units/kg body weight, more preferably in a range of 10-50 units/kg body weight, and most preferably at a dosage of 20-40 units/kg body weight; the interval frequency is in the range from about 8 to 24 hours (in severely affected hemophiliacs); and the duration of treatment in days is in the range from 1 to 10 days or until the bleeding episode is resolved. See, e.g., Roberts, H. R., and M. R. Jones, “Hemophilia and Related Conditions—Congenital Deficiencies of Prothrombin (Factor II, Factor V, and Factors VII to XII),” Ch. 153, 1453-1474, 1460, in Hematology , Williams, W. J., et al., ed. (1990). Patients with inhibitors may require a different amount of recombinant porcine or modified porcine factor VIII than their previous form of factor VIII. For example, patients may require less recombinant porcine or modified porcine factor VIII because of its higher specific activity than human factor VIII and its decreased antibody reactivity. As in treatment with human or plasma-derived porcine factor VIII, the amount of therapeutic factor VIII infused is defined by the one-stage factor VIII coagulation assay and, in selected instances, in vivo recovery is determined by measuring the factor VIII in the patient's plasma after infusion. It is to be understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that the concentration ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition.

Treatment can take the form of a single intravenous administration of the composition or periodic or continuous administration over an extended period of time, as required. Alternatively, therapeutic factor VIII can be administered subcutaneously or orally with liposomes in one or several doses at varying intervals of time.

Recombinant porcine or modified porcine factor VIII can also be used to treat uncontrolled bleeding due to factor VIII deficiency in hemophiliacs who have developed antibodies to human factor VIII. In this case, coagulant activity that is superior to that of human or animal factor VIII alone is not necessary. Coagulant activity that is inferior to that of human factor VIII (i.e., less than 3,000 units/mg) will be useful if that activity is not neutralized by antibodies in the patient's plasma.

It has been demonstrated herein that recombinant porcine and modified porcine factor VIII's can differ in specific activity from human factor VIII. Factor VIII proteins having greater procoagulant activity from human factor VIII are useful in treatment of hemophilia because lower dosages will be required to correct a patient's factor VIII deficiency. Factor VIII's having lower procoagulant activity than human factor VIII are also suitable for therapeutic use provided they have at least 1% of specific activity compared to normal human factor VIII. A factor VIII of the present invention having procoagulant activity is therefore defined as having at least 1% of the specific activity of human factor VIII.

The recombinant porcine or modified porcine factor VIII molecule and the methods for isolation, characterization, making, and using it generally described above will be further understood with reference to the following non-limiting examples.

EXAMPLE 1

Assay of Porcine Factor VIII and Hybrid Human/porcine Factor VII

Porcine factor VIII has more coagulant activity than human factor VIII, based on specific activity of the molecule. This conclusion is based on the use of appropriate standard curves that allow human porcine factor VIII to be fairly compared. Coagulation assays are based on the ability of factor VIII to shorten the clotting time of plasma derived from a patient with hemophilia A. Two types of assays were employed: the one-stage and the two stage assay.

In the one-stage assay, 0.1 ml hemophilia A plasma (George King Biomedical, Inc.) was incubated with 0.1 ml activated partial thromboplastin reagent (APTT) (Organon Teknika) and 0.01 ml sample or standard, consisting of diluted, citrated normal human plasma, for 5 min at 37° C. in a water bath. Incubation was followed by addition of 0.1 ml 20 mM CaCl 2 , and the time for development of a fibrin clot was determined by visual inspection.

A unit of factor VIII is defined as the amount present in 1 ml of citrated normal human plasma. With human plasma as the standard, porcine and human factor VIII activity were compared directly. Dilutions of the plasma standard or purified proteins were made into 0.15 M NaCl, 0.02 M HEPES, pH 7.4. The standard curve was constructed based on 3 or 4 dilutions of plasma, the highest dilution being 1/50, and on log 10 clotting time plotted against log 10 plasma concentration, which results in a linear plot. The units of factor VIII in an unknown sample were determined by interpolation from the standard curve.

The one-stage assay relies on endogenous activation of factor-VIII by activators formed in the hemophilia A plasma, whereas the two-stage assay measures the procoagulant activity of preactivated factor VIII. In the two-stage assay, samples containing factor VIII that had been reacted with thrombin were added to a mixture of activated partial thromboplastin and human hemophilia A plasma that had been preincubated for 5 min at 37° C. The resulting clotting times were then converted to units/ml, based on the same human standard curve described above. The relative activity in the two-stage assay was higher than in the one-stage assay because the factor VIII had been preactivated.

EXAMPLE 2

Characterization of the Functional Difference Between Human and Porcine Factor VII

The isolation of porcine and human plasma-derived factor VIII and human recombinant factor VIII have been described in the literature in Fulcher, C. A. et al. (1982) Proc. Natl. Acad. Sci. USA 79:1648-1652; Toole et al. (1984) Nature 312:342-347 (Genetics Institute); Gitschier et al. (1984) Nature 312:326-330 (Genentech); Wood et al. (1984) Nature 312:330-337 (Genentech); Vehar et al. 312 Nature 312:337-342 (Genentech); Fass et al. (1982) Blood 59:594; Toole et al. (1986) Proc. Natl. Acad. Sci. USA 83:5939-5942. This can be accomplished in several ways. All these preparations are similar in subunit composition, although there is a functional difference in stability between human and porcine factor VIII.

For comparison of human recombinant and porcine factor VIII, preparations of highly-purified human recombinant factor VIII (Cutter Laboratories, Berkeley, Calif.) and porcine factor VIII [immunopurified as described in Fass et al. (1982) Blood 59:594] were subjected to high-pressure liquid chromatography (HPLC) over a Mono Q™ (Pharmacia-LKB, Piscataway, N.J.) anion-exchange column (Pharmacia, Inc.). The purposes of the Mono Q™ HPLC step were elimination of minor impurities of exchange of human and porcine factor VIII into a common buffer for comparative purposes. Vials containing 1000-2000 units of factor VIII were reconstituted with 5 ml H 2 O. Hepes (2 M at pH 7.4) was then added to a final concentration of 0.02 M. Factor VIII was applied to a Mono Q™ HR 5/5 column equilibrated in 0.15 M NaCl, 0.02 M Hepes, 5mM CaCl 2 , at pH 7.4 (Buffer A plus 0.15 M NaCl); washed with 10 ml Buffer A+0.15 M NaCl; and eluted with a 20 ml linear gradient, 0.15 M to 0.90 M NaCl in Buffer A at a flow rate of 1 ml/min.

For comparison of human plasma-derived factor VIII (purified by Mono Q™ HPLC) and porcine factor VIII, immunoaffinity-purified, plasma-derived porcine factor VIII was diluted 1:4 with 0.04 M Hepes, 5 mM CaCl 2 , 0.01% Tween-80, at pH 7.4, and subjected to Mono Q™ HPLC under the same conditions described in the previous paragraph for human factor VIII. These procedures for the isolation of human and porcine factor VIII are standard for those skilled in the art.

Column fractions were assayed for factor VIII activity by a one-stage coagulation assay. The average results of the assays, expressed in units of activity per A 280 of material, are given in Table II, and indicate that porcine factor VIII has at least six times greater activity than human factor VIII when the one-stage assay is used.

TABLE II
COMPARISON OF HUMAN AND PORCINE FACTOR VIII
COAGULANT ACTIVITY
Activity (U/A                                                                        280                                                                    )
Porcine              21,300
Human plasma-derived 3,600
Human recombinant    2,400

EXAMPLE 3

Comparison of the Stability of Human and Porcine Factor VIII

The results of the one-stage assay for factor VIII reflect activation of factor VIII to factor VIIIa in the sample and possibly loss of formed factor VIIIa activity. A direct comparison of the stability of human and porcine factor VIII was made. Samples from Mono Q™ HPLC (Pharmacia, Inc., Piscataway, N.J.) were diluted to the same concentration and buffer composition and reacted with thrombin. At various times, samples were removed for two-stage coagulation assay. Typically, peak activity (at 2 min) was 10-fold greater for porcine than human factor VIIIa, and the activities of both porcine and human factor VIIIa subsequently decreased, with human factor VIIIa activity decreasing more rapidly.

Generally, attempts to isolate stable human factor VIIIa are not successful even when conditions that produce stable porcine factor VIIIa are used. To demonstrate this, Mono QT HPLC-purified human factor VIII was activated with thrombin and subjected to Mono S™ cation-exchange (Pharmacia, Inc.) HPLC under conditions that produce stable porcine factor VIIIa, as described by Lollar et al. (1989) Biochemistry 28:666.

Human factor VIII, 43 μg/ml (0.2 μM) in 0.2 M NaCl, 0.01 M Hepes, 2.5 mM CaCl 2 , at pH 7.4, in 10 ml total volume, was reacted with thrombin (0.036 μM) for 10 min, at which time FPR-CH 2 Cl D-phenyl-prolyl-arginyl-chloromethyl ketone was added to a concentration of 0.2 μM for irreversible inactivation of thrombin. The mixture then was diluted 1:1 with 40 mM 2-(N-morpholino) ethane sulfonic acid (MES), 5 mM CaCl 2 , at pH 6.0, and loaded at 2 ml/min onto a Mono S™ HR 5/5 HPLC column (Pharmacia, Inc.) equilibrated in 5 mM MES, 5 mM CaCl 2 , at pH 6.0 (Buffer B) plus 0.1 M NaCl. Factor VIIIa was eluted without column washing with a 20 ml gradient from 0.1 M NaCl to 0.9 M NaCl in Buffer B at 1 ml/min.

The fraction with coagulant activity in the two-stage assay eluted as a single peak under these conditions. The specific activity of the peak fraction was approximately 7,500 U/A 280 . Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) of the Mono S™ factor VIIIa peak, followed by silver staining of the protein, revealed two bands corresponding to a heterodimeric (A3-C1-C2/A1) derivative of factor VIII. Although the A2 fragment was not identified by silver staining under these conditions because of its low concentration, it was identified as a trace constituent by 125 I-labeling.

In contrast to the results with human factor VIII, porcine factor VIIIa isolated by Mono S™ HPLC under the same conditions had a specific activity 1.6×10 6 U/A 280 . Analysis of porcine factor VIIIa by SDS-PAGE revealed 3 fragments corresponding to A1, A2, and A3-C1-C2 subunits, demonstrating that porcine factor VIIIa possesses three subunits.

The results of Mono S™ HPLC of human thrombin-activated factor VIII preparations at pH 6.0 indicate that human factor VIIIa is labile under conditions that yield stable porcine factor VIIIa. However, although trace amounts of A2 fragment were identified in the peak fraction, determination of whether the coagulant activity resulted from small amounts of heterotrimeric factor VIIIa or from heterodimeric factor VIIIa that has a low specific activity was not possible from this method alone.

A way to isolate human factor VIIIa before it loses its A2 subunit is desirable to resolve this question. To this end, isolation was accomplished in a procedure that involves reduction of the pH of the Mono S™ buffers to pH 5. Mono Q™-purified human factor VIII (0.5 mg) was diluted with H 2 O to give a final composition of 0.25 mg/ml (1 μm) factor VIII in 0.25 M NaCl, 0.01 M Hepes, 2.5 mM CaCl 2 , 0.005% Tween-80, at pH 7.4 (total volume 7.0 ml). Thrombin was added to a final concentration of 0.072 μm and allowed to react for 3 min. Thrombin was then inactivated with FPR-CH 2 Cl (0.2 μm). The mixture then was diluted 1:1 with 40 mM sodium acetate, 5 mM CaCl 2 , 0.01% Tween-80, at pH 5.0, and loaded at 2 ml/min onto a Mono S™ HR 5/5 HPLC column equilibrated in 0.01 M sodium acetate, 5 mM CaCl 2 , 0.01% Tween-80, at pH 5.0, plus 0.1 M NaCl. Factor VIIIa was eluted without column washing with a 20 ml gradient from 0.1 M NaCl to 1.0 M NaCl in the same buffer at 1 ml/min. This resulted in recovery of coagulant activity in a peak that contained detectable amounts of the A2 fragment as shown by SDS-PAGE and silver staining. The specific activity of the peak fraction was tenfold greater than that recovered at pH 6.0 (75,000 U/A 280 v. 7,500 U/A 280 ). However, in contrast to porcine factor VIIIa isolated at pH 6.0, which is indefinitely stable at 4° C., human factor VIIIa activity decreased steadily over a period of several hours after elution from Mono S™. Additionally, the specific activity of factor VIIIa purified at pH 5.0 and assayed immediately is only 5% that of porcine factor VIIIa, indicating that substantial dissociation occurred prior to assay.

These results demonstrate that both human and porcine factor VIIIa are composed of three subunits (A1, A2, and A3-C1-C2). Dissociation of the A2 subunit is responsible for the loss of activity of both human and porcine factor VIIIa under certain conditions, such as physiological ionic strength, pH, and concentration. The relative stability of porcine factor VIIIa under certain conditions is because of stronger association of the A2 subunit.

EXAMPLE 4

Isolation and Sequencing of DNA Encoding the A2 Domain of Porcine Factor VIII

Only the nucleotide sequence encoding the B domain and part of the A2 domain of porcine factor VIII has been sequenced previously [Toole et al. (1986) Proc. Natl. Acad. Sci. USA 83:5939-5942]. The cDNA and predicted amino acid sequences (SEQ ID NOs: 3 and 4, respectively) for the entire porcine factor VIII A2 domain are disclosed herein.

The porcine factor VIII A2 domain was cloned by reverse transcription of porcine spleen total RNA and PCR amplification; degenerate primers based on the known human factor VIII cDNA sequence and an exact porcine primer based on a part of the porcine factor VIII sequence were used. A 1 kb PCR product was isolated and amplified by insertion into a Bluescript™ (Stratagene) phagemid vector.

The porcine A2 domain was completely sequenced by dideoxy sequencing. The cDNA and predicted amino acid sequences are as described in SEQ ID NOs: 3 and 4, respectively.

EXAMPLE 5

Complete Sequence of DNA Encoding Porcine Factor VIII

Klenow fragment, phosphorylated ClaI linkers, NotI linkers, T4 ligase, and Taq DNA polymerase were purchased from Promega (Madison, Wis.). Polynucleotide kinase was purchased from Life Technologies, Inc., Gaithersburg, Md. γ 32 P-ATP (Redivue, >5000Ci/mmol) was purchased from Amersham. pBluescript II KS- and E. coli Epicurean XL1-Blue cells were purchased from Stratagene (La Jolla, Calif.). Synthetic oligonucleotides were purchased from Life Technologies, Inc. or Cruachem, Inc. 5′-phosphorylated primers were used when PCR products were produced for cloning purposes. Nucleotide (nt) numbering of oligonucleotides used as primers for polymerase chain reaction (PCR) amplification of porcine fVIII cDNA or genomic DNA uses the human fVIII cDNA as reference (Wood et al. (1984) supra).

Porcine spleen total RNA was isolated by acid guanidinium thiocyanate-phenol-chloroform extraction [Chomczynski et al. (1987) Anal. Biochem . 162:156-159]. Porcine cDNA was prepared from total spleen RNA using Moloney murine leukemia virus reverse transcriptase (RT) and random hexamers to prime the reaction (First-Strand cDNA Synthesis Kit, Pharmacia Biotech) unless otherwise indicated. RT reactions contained 45 mM Tris-Cl , pH 8.3, 68 mM KCl, 15 mM DTT, 9 mM MgCl 2 , 0.08 mg/ml bovine serum albumin and 1.8 mM deoxynucleotide triphosphate (dNTP). Porcine genomic DNA was isolated from spleen using a standard procedure (Strauss, W. M. (1995) In Current Protocols in Molecular Biology , F. M. Ausubel et al., editors, John Wiley & Sons, pp. 2.2.1-2.2.3). Isolation of DNA from agarose gels was done using Geneclean II (Bio 101) or Quiex II Gel Extraction Kit (Qiagen).

PCR reactions were done using a Hybaid OmniGene thermocycler. For PCR reactions employing Taq DNA polymerase, reactions included 0.6 mM MgCl 2 , 0.2 mM dNTPs, 0.5 μM oligonucleotide primers, 50 U/ml polymerase and 0.1 volume of first strand cDNA reaction mix. Except where indicated otherwise, PCR products were gel purified, blunt-ended with Klenow fragment, precipitated with ethanol, and either ligated to the EcoRV site of dephosphorylated pBluescript II KS- or ligated with phosphorylated ClaI linkers using T4 ligase, digested with ClaI, purified by Sephacryl S400 chromatography, and ligated to ClaI-cut, dephosphorylated pBluescript II KS-. Ligations were done using T4 DNA ligase (Rapid DNA ligation kit, Boehringer Mannheim) except where indicated otherwise. Insert-containing pBluescript II KS- plasmids were used to transform E. coli Epicurean XL1-Blue cells.

Sequencing of plasmid DNA was done using an Applied Biosystems 373a automated DNA sequencer and the PRISM dye terminator kit or manually using Sequenase v. 2.0 sequencing kit (Amersham Corporation). Direct sequencing of PCR products, including 32 P-end labelling of oligonucleotides was done using a cycle sequencing protocol (dsDNA Cycle Sequencing System, Life Technologies).

Isolation of Porcine fVIII cDNA Clones Containing 5′ UTR Sequence, Signal peptide and A1 Domain Codons.

The porcine fVIII cDNA 5′ to the A2 domain was amplified by nested RT-PCR of female pig spleen total RNA using a 5′ rapid amplification of cDNA ends (5′-RACE) protocol (Marathon cDNA Amplification, Clontech, Version PR55453). This included first strand cDNA synthesis using a lock-docking oligo(dT) primer [Borson, N. D. et al. (1992) PCR Methods Appl . 2:144-148], second strand cDNA synthesis using E. coli DNA polymerase I, and ligation with a 5′ extended double stranded adaptor, SEQ ID NO:5

5′-CTA ATA CGA CTC ACT ATA GGG CTC GAG CGG CCG CCC GGG CAG GT-3 3′-H 2 N-CCCGTCCA-PO 4 -5′

whose short strand was blocked at the 3′ end with an amino group to reduce non-specific PCR priming and which was complementary to the 8 nucleotides at the 3′ end (Siebert, P. D., et al. (1995) Nucleic. Acids. Res . 23:1087-1088). The first round of PCR was done using an adaptor-specific oligonucleotide, SEQ ID NO:6 5′-CCA TCC TAA TAC GAC TCA CTA TAG GGC-3′ (designated AP1) as sense primer, and a porcine fVIII A2 domain specific oligonucleotide SEQ ID NO:7 5′-CCA TTG ACA TGA AGA CCG TTT CTC-3′ (nt 2081-2104) as antisense primer. The second round of PCR was done using a nested, adaptor-specific oligonucleotide, SEQ ID NO:8 5′-ACT CAC TAT AGG GCT CGA GCG GC-3′ (designated AP2) as sense primer, and a nested, porcine A2 domain-specific oligonucleotide SEQ ID NO:9 5′-GGG TGC AAA GCG CTG ACA TCA GTG-3′ (nt 1497-1520) as antisense primer. PCR was carried out using a commercial kit (Advantage cDNA PCR core kit) which employs an antibody-mediated hot start protocol [Kellogg, D. E. et al. (1994) BioTechniques 16:1134-1137]. PCR conditions included denaturation at 94° C. for 60 sec, followed by 30 cycles (first PCR) or 25 cycles (second PCR) of denaturation for 30 sec at 94° C., annealing for 30 sec at 60° C. and elongation for 4 min at 68using tube temperature control. This procedure yielded a prominent ≈1.6 kb product which was consistent with amplification of a fragment extending approximately 150 bp into the 5′ UTR. The PCR product was cloned into pBluescript using ClaI linkers. The inserts of four clones were sequenced in both directions.

The sequence of these clones included regions corresponding to 137 bp of the 5′ UTR, the signal peptide, the A1 domain and part of the A2 domain. A consensus was reached in at least 3 of 4 sites. However, the clones contained an average of 4 apparent PCR-generated mutations, presumably due to the multiple rounds of PCR required to generate a clonable product. Therefore, we used sequence obtained from the signal peptide region to design a sense strand phosphorylated PCR primer, SEQ ID NO: 10 5′-CCT CTC GAG CCA CCA TGT CGA GCC ACC ATG CAG CTA GAG CTC TCC ACC TG-3′, designated RENEOPIGSP, for synthesis of another PCR product to confirm the sequence and for cloning into an expression vector. The sequence in bold represents the start codon. The sequence 5′ to this represents sequence identical to that 5′ of the insertion site into the mammalian expression vector ReNeo used for expression of fVIII (Lubin et al. (1994) supra). This site includes an Xhol cleavage site (underlined). RENEOPIGSP and the nt 1497-1520 oligonucleotide were used to prime a Taq DNA polymerase-mediated PCR reaction using porcine female spleen cDNA as a template. DNA polymerases from several other manufacturers failed to yield a detectable product. PCR conditions included denaturation at 94° C. for four min, followed by 35 cycles of denaturation for 1 min at 94° C., annealing for 2 min at 55° C. and elongation for 2 min at 72° C., followed by a final elongation step for 5 min at 72° C The PCR product was cloned into pBluescript using ClaI linkers. The inserts of two of these clones were sequenced in both directions and matched the consensus sequence.

Isolation of Porcine fVIII cDNA Clones Containing A3. C1 and 5′ Half of the C2 Domain Codons.

Initially, two porcine spleen RT-PCR products, corresponding to a B-A3 domain fragment (nt 4519-5571) and a C1-C2 domain fragment (nt 6405-6990) were cloned. The 3′end of the C2 domain that was obtained extended into the exon 26 region, which is the terminal exon in fVIII. The B-A3 product was made using the porcine-specific B domain primer, SEQ ID NO: 11 5′ CGC GCG GCC GCG CAT CTG GCA AAG CTG AGT T 3′, where the underlined region corresponds to a region in porcine fVIII that aligns with nt 4519-4530 in human fVIII. The 5′ region of the oligonucleotide includes a NotI site that was originally intended for cloning purposes. The antisense primer used in generating the B-A3 product, SEQ ID NO: 12 5′-GAA ATA AGC CCA GGC TTT GCA GTC RAA-3′ was based on the reverse complement of the human fVIII cDNA sequence at nt 5545-5571. The PCR reaction contained 50 mM KCl, 10 mM Tris-Cl, pH 9.0, 0.1% Triton X-100, 1.5 mM MgCl 2 , 2.5 mM dNTPs, 20 μM primers, 25 units/ml Taq DNA polymerase and 1/20 volume of RT reaction mix. PCR conditions were denaturation at 94° C. for 3 min, followed by 30 cycles of denaturation for 1 min at 94° C., annealing for 2 min at 50° C. elongation for 2 min at 72° C. The PCR products were phosphorylated using T4 DNA kinase and NotI linkers were added. After cutting with NotI, the PCR fragments were cloned into the NotI site of BlueScript II KS- and transformed into XL1-Blue cells.

The C1-C2 product was made using the known human cDNA sequence to synthesize sense and antisense primers, SEQ ID NO: 13 5′-AGG AAA TTC CAC TGG AAC CTT N-3′ (nt 6405-6426) and SEQ ID NO:14 5′-CTG GGG GTG AAT TCG AAG GTA GCG N-3′ (reverse complement of nt 6966-6990), respectively. PCR conditions were identical to those used to generate the B-A2 product. The resulting fragment was ligated to the pNOT cloning vector using the Prime PCR Cloner Cloning System (5 Prime-3 Prime, Inc., Boulder, Colo.) and grown in JM109 cells.

The B-A3 and C 1-C2 plasmids were partially sequenced to make the porcine-specific sense and antisense oligonucleotides, SEQ ID NO:15 5′-GAG TTC ATC GGG AAG ACC TGT TG-3′ (nt 4551-4573) and SEQ ID NO:16 5′-ACA GCC CAT CAA CTC CAT GCG AAG-3′ (nt 6541-6564), respectively. These oligonucleotides were used as primers to generate a 2013 bp RT-PCR product using a Clontech Advantage cDNA PCR kit. This product, which corresponds to human nt 4551-6564, includes the region corresponding to the light chain activation peptide (nt 5002-5124), A3 domain (nt 5125-6114) and most of the C1 domain (nt 6115-6573); The sequence of the C1-C2 clone had established that human and porcine cDNAs from nt 6565 to the 3′ end of the C1 domain were identical. The PCR product cloned into the EcoRV site of pBluescript II KS-. Four clones were completely sequenced in both directions. A consensus was reached in at least 3 of 4 sites.

Isolation of Porcine fVIII cDNA Clones Containing the 3′ Half of the C2 Domain Codons.

The C2 domain of human fVIII (nucleotides 6574-7053) is contained within exons 24-26 [Gitschier J. et al. (1984) Nature 312:326-330]. Human exon 26 contains 1958 bp, corresponding nucleotides 6901-8858. It includes 1478 bp of 3′ untranslated sequence. Attempts to clone the exon 26 cDNA corresponding to the 3′ end of the C2 domain and the 3 ′UTR by 3′ RACE [Siebert et al. (1995) supra], inverse PCR [Ochman, H. et al. (1990) Biotechnology (N.Y). 8:759-760], restriction site PCR [Sarkar, G. et al. (1993) PCR Meth. Appl . 2:318-322], “unpredictably primed” PCR [Dominguez, O. et al. (1994) Nucleic. Acids Res . 22:3247-3248]:and by screening a porcine liver cDNA library failed. 3′ RACE was attempted using the same adaptor-ligated double stranded cDNA library that was used to successfully used to clone the 5′ end of the porcine fVIII cDNA. Thus, the failure of this method was not due to the absence of cDNA corresponding to exon 26.

A targeted gene walking PCR procedure [Parker, J. D. et al. (1991) Nucleic. Acids. Res . 19:3055-3060] was used to clone the 3′ half of the C2 domain. A porcine-specific sense primer, SEQ ID NO: 17 5′-TCAGGGCAATCAGGACTCC-3′ (nt 6904-6924) was synthesized based on the initial C2 domain sequence and was used in a PCR reaction with nonspecific “walking” primers selected from oligonucleotides available in the laboratory. The PCR products were then targeted by primer extension analysis [Parker et al. (1991) BioTechniques 10:94-101] using a 32 p-end labelled porcine-specific internal primer, SEQ ID NO:18 5′-CCGTGGTGAACGCTCTGGACC-3′ (nt 6932-6952). Interestingly, of the 40 nonspecific primers tested, only two yielded positive products on primer extension analysis and these two corresponded to an exact and a degenerate human sequence at the 3′ end of the C2 domain: SEQ ID NO:19 5′-GTAGAGGTCCTGTGCCTCGCAGCC-3′ (nt 7030-7053) and SEQ ID NO:20 5′-GTAGAGSTSCTGKGCCTCRCAKCCYAG-3′, (nt 7027-7053). These primers had initially been designed to yield a product by conventional RT-PCR but failed to yield sufficient product that could be visualized by ethidium bromide dye binding. However, a PCR product could be identified by the more sensitive primer extension method. This product was gel-purified and directly sequenced. This extended the sequence of porcine fVIII 3′ to nt 7026.

Additional sequence was obtained by primer extension analysis of a nested PCR product generated using the adaptor-ligated double-stranded cDNA library used in the 5′-RACE protocol described previously. The first round reaction used the porcine exact primer SEQ ID NO:21 5′-CTTCGCATGGAGTTGATGGGCTGT-3′ (nt 6541-6564) and the AP1 primer. The second round reaction used SEQ ID NO:22 5′-AATCAGGACTCCTCCACCCCCG-3′ (nt 6913-6934) and the AP2 primer. Direct PCR sequencing extended the sequence 3′ to the end of the C2 domain (nt 7053). The C2 domain sequence was unique except at nt 7045 near the 3′ end of the C2 domain. Analysis of repeated PCR reactions yielded either A, G or a double read of A/G at this site.

Sequencing was extended into the 3′UTR using two additional primers, SEQ ID NO:23 5′-GGA TCC ACC CCA CGA GCT GG-3′ (nt 6977-6996) and SEQ ID NO:24 5′-CGC CCT GAG GCT CGA GGT TCT AGG-3′ (nt 7008-7031). Approximately 15 bp of 3′ UTR sequence were obtained, although the sequence was unclear at several sites. Several antisense primers then were synthesized based on the best estimates of the 3′ untranslated sequence. These primers included the reverse complement of the TGA stop codon at their 3′ termini. PCR products were obtained from both porcine spleen genomic DNA and porcine spleen cDNA that were visualized by agarose gel electrophoresis and ethidium bromide staining using a specific sense primer SEQ ID NO:25 5′-AAT CAG GAC TCC TCC ACC CCC G-3′ (nt 6913-6934) and the 3′ UTR antisense primer, SEQ ID NO:26 5′-CCTTGCAGGAATTCGATTCA-3′. To obtain sufficient quantities of material for cloning purposes, a second round of PCR was done using a nested sense primer, SEQ ID NO:27 5′-CCGTGGTGAACGCTCTGGACC-3′ (nt 6932-6952) and the same antisense primer. The 141 bp PCR product was cloned into EcoRV-cut pBluescript II KS-. Sequence of three clones derived from genomic DNA and three clones derived from cDNA was obtained in both directions. The sequence was unambiguous except at nt 7045, where genomic DNA was always A and cDNA was always G.

Multiple DNA Sequence Alignments of Human, Porcine, and Mouse fVIII (FIGS. 1 A- 1 H).

Alignments of the signal peptide, A1, A2, A3, C1, and C2 regions were done using the CLUSTALW program [Thompson, J. D. et al. (1994) Nucleic. Acids. Res . 22:4673-4680]. Gap open and gap extension penalties were 10 and 0.05 respectively. The alignments of the human, mouse, and pig B domains have been described previously [Elder et al. (1993) supra]. The human A2 sequence corresponds to amino acids 373-740 in SEQ ID NO:2. The porcine A2 amino acid sequence is given in SEQ ID NO:4, and the mouse A2 domain amino acid sequence is given in SEQ ID NO:28, amino acids 392-759.

EXAMPLE 6

Expression of Active, Recombinant B-domainless Porcine Factor VIII (PB − )

Materials

Citrated hemophilia A and normal pooled human plasmas were purchased from George King Biomedical, Inc. Fetal bovine serum, geneticin, penicillin, streptomycin, DMEM/F12 medium and AIM-V medium were purchased from Life Technologies, Inc. Taq DNA polymerase was purchased from Promega. Vent DNA polymerase was purchased from New England Biolabs. Pfu DNA polymerase and the phagemid pBlueScript II KS − were purchased from Stratagene. Synthetic oligonucleotides were purchased from Life Technologies or Cruachem, Inc. Restriction enzymes were purchased from New England Biolabs or Promega. 5′-phosphorylated primers were used when PCR products were produced for cloning purposes. Nucleotide (nt) numbering of oligonucleotides used as primers for polymerase chain reaction (PCR) amplification of porcine fVIII cDNA or genomic DNA uses the human fVIII cDNA as reference [Wood et al. (1984) Nature 312:330-337]. A fVIII expression vector, designated HB − /ReNeo, was obtained from Biogen, Inc. HB − /ReNeo contains ampicillin and geneticin resistance genes and a human fVIII cDNA that lacks the entire B domain, defined as the Ser741-Arg1648 cleavage fragment produced by thrombin. To simplify mutagenesis of fVIII C2 domain cDNA, which is at the 3′ end of the fVIII insert in ReNeo, a NotI site was introduced two bases 3′ to the stop codon of HB − /ReNeo by splicing-by-overlap extension (SOE) mutagenesis [Horton, R. M. et al. (1993) Methods Enzymol . 217:270-279]. This construct is designated HB − ReNeo/NotI.

Total RNA was isolated by acid guanidinium thiocyanate-phenol-chloroform extraction [Chomczynski, P. et al. (1987) Anal. Biochem . 162:156-159]. cDNA was synthesized from mRNA using Moloney murine leukemia virus reverse transcriptase (RT) and random hexamers according to instructions supplied by the manufacturer (First-Strand cDNA Synthesis Kit, Pharmacia Biotech). Plasmid DNA was purified using a Qiagen Plasmid Maxi Kit (Qiagen, Inc.). PCR reactions were done using a Hybaid OmniGene thermocycler using Taq, Vent, or pfu DNA polymerases. PCR products were gel purified, precipitated with ethanol, and ligated into plasmid DNA using T4 DNA ligase (Rapid DNA ligation kit, Boehringer Mannheim). Insert-containing plasmids were used to transform E. coli Epicurean XL1-Blue cells. All novel fVIII DNA sequences generated by PCR were confirmed by dideoxy sequencing using an Applied Biosystems 373a automated DNA sequencer and the PRISM dye terminator kit.

Construction of a Hybrid fVIII Expression Vector, HP20, Containing the Porcine C2 Domain.

A porcine fVIII cDNA corresponding to the 3′ end of the C1 domain and all of the C2 domain was cloned into pBluescript by RT-PCR from spleen total RNA using primers based on known porcine fVIII cDNA sequence [Healey, J. F. et al. (1996) Blood 88:42094214]. This construct and HB − /ReNeo were used as templates to construct a human C1-porcine C2 fusion product in pBlueScript by SOE mutagenesis. The C1-C2 fragment in this plasmid was removed with ApaI and NotI and ligated into ApaI/NotI-cut HB − /ReNeo/NotI to produce HP20/ReNeo/NotI.

Construction of B-domain Deleted Hybrid Human/porcine fVIII Containing the Porcine Light Chain (HP18)-

The human fVIII light chain consists of amino acid residues Asp1649-Tyr2332. The corresponding residues in the porcine fVIII cDNA were substituted for this region of HB − to produce a hybrid human/porcine fVIII molecule designated HP18. This was done by substituting a PCR product corresponding to porcine A2 region, the A3 domain, the C 1 domain, and part of the C2 domain for the corresponding region in HP20. To facilitate constructions, a synonymous AvrII site was introduced into nt 2273 at the junction of the A2 and A3 domains of HP20 by SOE mutagenesis.

Construction of B-domain Deleted Hybrid Human/porcine fVIII Containing the Porcine Signal Peptide, A1 Domain and A2 Domain (HP22)-

The human fVIII signal peptide, A1 domain and A2 domains consist of amino acid residues Met(-19)-Arg740. The corresponding residues in the porcine fVIII cDNA were substituted for this region of HB- to produce a molecule designated HP22. Additionally, a synonymous AvrII site was introduced into nt 2273 at the junction of the A2 and A3 domains of HP22 by SOE mutagenesis. HP22 was constructed by fusion of a porcine signal peptide-A1-partial A2 fragment in pBlueScript [Healy et al. (1996) supra] with a B-domainless hybrid human/porcine fVIII containing the porcine A2 domain, designated HP1 [Lubin et al. (1994) supra].

Construction of Porcine B Domainless fVIII-(PB − )

A SpeI/NotI fragment of HP18/BS (+AvrII) was digested with AvrII/NotI and ligated into AvrII/NotI-digested HP22/BS (+AvrII) to produce a construct PB − /BS (+AvrII), which consists of the porcine fVIII lacking the entire B domain. PB- was cloned into ReNeo by ligating an Xba/NotI fragment of PB − /BS (+AvrII) into HP22/ReNeo/NotI (+AvrII).

Expression of Recombinant fVIII Molecules

PB − /ReNeo/NotI (+AvrII) and HP22/ReNeo/NotI (+AvrII) were transiently transfected into COS cells and expressed as described previously [Lubin, I. M. et al. (1994) J. Biol. Chem . 269:8639-8641]. HB − /ReNeo/NotI and no DNA (mock) were transfected as a control.

The fVIII activity of PB − , HP22, and HB − were measured by a chromogenic assay as follows. Samples of fVIII in COS cell culture supernatants were activated by 40 nM thrombin in a 0.15 M NaCl, 20 mM HEPES, 5Mm cAC12, 0.01% Tween-80, pH 7.4 in the presence of 10 nM factor IXa, 425 nM factor X, and 50 μM unilamellar phosphatidylserine-[phosphatidycholine (25/75 w/w) vesicles. After 5 min, the reaction was stopped with 0.05 M EDTA and 100 nM recombinant desulfatohirudin and the resultant factor Xa was measured by chromogenic substrate assay. In the chromogenic substrate assay, 0.4 mM Spectrozyme Xa was added and the rate of para-nitroanilide release was measured by measuring the absorbance of the solution at 405 nm.

Results of independently transfected duplicate cell culture supernatants (absorbance at 405 nm per minute)

HB − : 13.9

PB − : 139

HP22: 100

mock: <0.2

These results indicate that porcine B-domainless fVIII and a B-domainless fVIII consisting of the porcine A1 and A2 subunits are active and suggest that they have superior activity to human B-domainless fVIII.

PB − was partially purified and concentrated from the growth medium by heparin-Sepharose chromatography. Heparin-Sepharose (10 ml) was equilibrated with 0.075 M NaCl, 10 MM HEPES, 2.5 mM CaCl 2 1 0.005% Tween-80, 0.02% sodium azide, pH 7.40. Medium (100-200 ml) from expressing cells was applied to the heparin-Sepharose, which then was washed with 30 ml of equilibration buffer without sodium azide. PB − was eluted with 0.65 M NaCl, 20 mM HEPES, 5 mM CaCl 2 , 0.01% Tween-80, pH 7.40 and was stored at →80° C. The yield of fVIII coagulant activity was typically 50-75%.

Stable Expression of Porcine B-domainless fVIII (PB − )

Transfected cell lines were maintained in Dulbecco's modified Eagle's medium-F12 containing 10% fetal bovine serum, 50 U/ml penicillin, 50 μg/ml streptomycin. Fetal bovine serum was heat inactivated at 50° C. for one hour before use. HB − /ReNeo and PB − ReNeo/NotI (+AvrII) were stably transfected into BHK cells and selected for geneticin resistance using a general protocol that has been described previously [Lubin et al. (1994) Biol. Chem . 269:8639-8641] except that expressing cells were maintained in growth medium containing 600 μg/ml geneticin. Cells from Corning T-75 flasks grown to confluence were transferred to Nunc triple flasks in medium containing 600 μg/ml geneticin and grown to confluence. The medium was removed and replaced with serum-free, AIM-V medium (Life Technologies, Inc.) without geneticin. Factor VIII expression was monitored by one-stage factor VIII coagulant activity (vide supra) and 100-150 ml of medium was collected once daily for four to five days. Maximum expression levels in medium for HB − and PB − were 102 units per ml and 10-12 units per ml of factor VIII coagulant activity, respectively.

Purification of PB −

PB − was precipitated from culture supernatant using 60% saturated ammonium sulfate and then purified by W3-3 immunoaffinity chromatography and mono Q high pressure liquid chromatography as described previously for the purification of plasma-derived porcine factor VIII [Lollar et al. (1993) Factor VIII/factor VIIIa. Methods Enzymol . 222:128-143]. The specific coagulant activity of PB − was measured by a one-stage coagulation assay [Lollar et al. (1993) supra] and was similar to plasma-derived porcine factor VIII.

When analyzed by SDS-polyacrylamide gel electrophoresis, the PB − preparation contained three bands of apparent molecular masses 160 kDa, 82 kDa, and 76 kDa. The 82 kDa and 76 kDa bands have been previously described as heterodimer containing the A1-A2 and ap-A3-Cl-C2 domains (where ap refers to an activation peptide) [Toole et al. (1984) Nature 312:342-347]. The 160 kDa band was transferred to a polyvinylidene fluoride membrane and subjected to NH2-terminal sequencing, which yielded Arg-Ile-Xx-Xx-Tyr (where Xx represents undermined) which is the NH2-terminal sequence of single chain factor VIII [Toole et al. (1984) supra]. Thus, PB − is partially processed by cleavage between the A2 and A3 domains, such that it consists of two forms, a single chain A1-A2-ap-A3-Cl-C2 protein and a A1-A2/ap-A3-Cl-C2 heterodimer. Similar processing of recombinant HB- has been reported [Lind et al. (1995) Eur. J. Biochem . 232:19-27].

Characterization of Porcine Factor VIII

We have determined the cDNA sequence of porcine fVIII corresponding to 137 bp of the 5′ UTR, the signal peptide coding region (57 bp), and the A1 (1119 bp), A3 (990 bp), C1 (456 bp), and C2 (483 bp) domains. Along with previously published sequence of the B domain and light chain activation peptide regions [Toole et al. (1986) supra] and the A2 domain [Lubin et al. (1994) supra], the sequence reported here completes the determination of the porcine. fVIII cDNA corresponding to the translated product. A fragment that included the 5′ UTR region, signal peptide, and A1 domain cDNA was cloned using a 5′-RACE RT-PCR protocol. A primer based on human C2 sequence was successful in producing an RT-PCR product that led to cloning of the A3, C1, and 5′ half of the C2 domain. The cDNA corresponding to the 3′ half of the C2 domain and 3′ UTR cDNA proved difficult to clone. The remainder of the C2 domain ultimately was cloned by a targeted gene walking PCR procedure [Parker et al. (1991) supra].

The sequence reported herein SEQ ID NO:29 was unambiguous except at nt 7045 near the 3′ end of the C2 domain, which is either A or G as described hereinabove. The corresponding codon is GAC (Asp) or AAC (Asn). The human and mouse codons are GAC and CAG (Gln), respectively. Whether this represents a polymorphism or a reproducible PCR artifact is unknown. Recombinant hybrid human/porcine B-domainless fVIII cDNAs containing porcine C2 domain substitutions corresponding to both the GAC and AAC codons have been stably expressed with no detectable difference in procoagulant activity. This indicates that there is not a functional difference between these two C2 domain variants.

The alignment of the predicted amino acid sequence of full-length porcine fVIII SEQ ID NO:30 with the published human [Wood et al. (1984) supra] and murine [Elder et al. (1993) supra] sequences is shown in FIGS. 1A-1H along with sites for post-translational modification, proteolytic cleavage, and recognition by other macromolecules. The degree of identity of the aligned sequences is shown in Table VII. As noted previously, the B domains of these species are more divergent than the A or C domains. This is consistent with the observation that the B domain has no known function, despite its large size [Elder et al. (1993) supra; Toole et al. (1986) supra]. The results of the present invention confirm that the B domain of porcine fVIII is not necessary for activity. Based on the sequence data presented herein, porcine fVIII having all or part of the B-domain deleted can be synthesized by expressing the porcine fVIII coding DNA having deleted therefrom all or part of codons of the porcine B domain. There is also more divergence of sequences corresponding to the A1 domain APC/factor IXa cleavage peptide (residues 337-372) and the light chain activation peptide (Table VII). The thrombin cleavage site at position 336 to generate the 337-372 peptide is apparently lost in the mouse since this residue is glutamine instead of arginine [Elder et al. (1993) supra]. The relatively rapid divergence of thrombin cleavage peptides (or in mouse fVIII a possibly vestigial 337-372 activation peptide) has been previously noted for the fibrinopeptides [Creighton, T. E. (1993) In Proteins: Structures and Molecular Properties , W. H. Freeman, New York, pp. 105-138]. Lack of biological function of these peptides once cleaved has been cited as a possible reason for the rapid divergence. Arg562 in human fVIII has been proposed to be the more important cleavage site for activated protein C during the inactivation of fVIII and fVIIIa [Fay, P.J. et al. (1991) J. Biol. Chem . 266:20139-20145]. This site is conserved in human, porcine and mouse fVIII.

Potential N-linked glycosylation sites (NXS/T where X is not proline) can be seen in FIGS. 1A-1H . There are eight conserved N-linked glycosylation sites: one in the A1 domain, one in the A2 domain, four in the B domain, one in the A3 domain, and one in the C1 domain. The 19 A and C domain cysteines are conserved, whereas there is divergence of B domain cysteines. Six of the seven disulfide linkages in fVIII are found at homologous sites in factor V and ceruloplasmin, and both C domain disulfide linkages are found in factor V [McMullen, B. A. et al. (1995) Protein Sci . 4:740-746]. Human fVIII contains sulfated tyrosines at positions 346, 718, 719, 723, 1664, and 1680 [Pittman, D. D. et al. (1992) Biochemistry 31:3315-3325; Michnick, D. A. et al. (1994) J. Biol. Chem . 269:20095-20102]. These residues are conserved in mouse fVIII and porcine fVIII (FIG. 1 ), although the CLUSTALW program failed to align the mouse tyrosine corresponding to Tyr346 in human fVIII.

Mouse and pig plasma can correct the clotting defect in human hemophilia A plasma, which is consistent with the level of conservation of residues in the A and C domains of these species. The procoagulant activity of porcine fVIII is superior to that of human fVIII [Lollar, P. et al. (1992) J. Biol. Chem . 267:23652-23657]. The recombinant porcine factor VIII (B domain-deleted) expressed and purified as herein described also displays greater specific coagulant activity than human fVIII, being comparable to plasma-derived porcine fVIII. This may be due to a decreased spontaneous dissociation rate of the A2 subunit from the active A1/A2/A3-Cl-C2 fVIII heterotrimer. Whether this difference in procoagulant activity reflects an evolutionary change in function as an example of species adaptation [Perutz, M. F. (1996) Adv. Protein Chem . 36:213-244] is unknown. Now that the porcine fVIII cDNA sequence corresponding to the translated product is complete, homolog scanning mutagenesis [Cunningham, B. C., et al. (1989) Science 243:1330-1336] may provide a way to identify structural differences between human and porcine fVIII that are responsible for the superior activity of the latter.

Porcine fVIII is typically less reactive with inhibitory antibodies that arise in hemophiliacs who have been transfused with fVIII or which arise as autoantibodies in the general population. This is the basis for using porcine fVIII concentrate in the management of patients with inhibitory antibodies [Hay and Lozier (1995) supra]. Most inhibitors are directed against epitopes located in the A2 domain or C2 domain [Fulcher, C. A. et al. (1985) Proc. Natl. Acad. Sci. USA 82:7728-7732; Scandella, D. et al. (1988) Proc. Natl. Acad. Sci. USA 85:6152-6156; Scandella, D. et al. (1989) Blood 74:1618-1626]. Additionally, an epitope of unknown significance has been identified that is in either the A3 or C1 domain [Scandella et al. (1989) supra; Scandella, D. et al. (1993) Blood 82:1767-1775; Nakai, H. et al. (1994) Blood 84:224a]. The A2 epitope has been mapped to residues 484-508 by homolog scanning mutagenesis [Healey et al. (1995) supra]. In this 25 residue segment, there is relatively low proportion of identical sequence (16/25 or 64%). It is interesting that this region, which appears to be functionally important based on the fact that antibodies to it are inhibitory, apparently has been subjected to relatively more rapid genetic drift. Alignment of the porcine A2 domain and A3 domains indicate that the A2 epitope shares no detectable homology with the corresponding region in the A3 domain.

The C2 inhibitor epitope of human fVIII has been proposed to be located to within residues 2248-2312 by deletion mapping [Scandella, D. et al. (1995) Blood 86:1811-1819]. Human and porcine fVIII are 83% identical in this 65 residue segment. However, homolog scanning mutagenesis of this region to characterize the C2 epitope has revealed that a major determinant of the C2 epitope was unexpectedly located in the region corresponding to human amino acids 2181-2243 (SEQ ID NO:2) and FIG. 1 H.

Human-porcine hybrid factor VIII proteins were made in which various portions of the C2 domain of human factor VIII were replaced by the corresponding portions of porcine factor VIII, using the strategy herein described. (Example 5) The synthesis of the various C2-hybrid factor VIIIs was accomplished by constructing hybrid coding DNA, using the nucleotide sequence encoding the porcine C2 region given in SEQ ID NO:30. Each hybrid DNA was expressed in transfected cells, such that the hybrid factor VIIIs could be partially purified from the growth medium. Activity,. in the absence of any inhibitor, was measured by the one-stage clotting assay.

A battery of five human inhibitors was used to test each hybrid factor VIII. The inhibitor plasmas containing anti factor VIII antibody had been previously shown to be directed against human C2 domain, based on the ability of recombinant human C2 domain to neutralize the inhibition. In all the test plasmas, the inhibitor titer was neutralized greater than 79% by C2 domain or light chain but less than 10% by recombinant human A2 domain. In addition the C2-hybrid factor VIIIs were tested against a murine monoclonal antibody, which binds the C2 domain, and like human C2 inhibitor antibodies, it inhibited the binding of factor VIII to phospholipid and to von Willebrand factor.

By comparing the antibody inhibitor titers against the C2-hybrid factor VIIIs, the major determinant of the human C2 inhibitor epitope was shown to be the region of residues 2181-2243 (SEQ ID NO:2, see also FIG. 1 H). Anti-C2 antibodies directed to a region COOH-terminal to residue 2253 were not identified in four of the five patient sera. In comparing hybrids having porcine sequence corresponding to human amino acid residues numbers 2181-2199 and 2207-2243, it was apparent that both regions contribute to antibody binding. The porcine amino acid sequence corresponding to human residues 2181-2243 is numbered 1982-2044 in SEQ ID NO:30. The sequence of porcine DNA encoding porcine amino acids numbered 1982-2044 is nucleotides numbered 5944-6132 in SEQ ID NO:29.

Referring to FIG. 1H , it can be seen that in the region 2181-2243, there, are 16 amino acid differences between the human and porcine sequences. The differences are found at residues 2181, 2182, 2188, 2195-2197, 2199, 2207, 2216, 2222, 2224-2227, 2234, 2238 and 2243. Amino acid replacement at one or more of these numbered residues can be carried out to make a modified human factor VIII non-reactive to human anti-C2 inhibitor antibodies. Alanine scanning mutagenesis provides a convenient method for generating alanine substitutions for naturally-occurring residues, as previously described. Amino acids other than alanine can be substituted as well, as described herein. Alanine substitutions for individual amino acids, especially those which are non-identical between human/porcine or human/mouse or which are most likely to contribute to antibody binding; can yield a modified factor VIII with reduced reactivity to inhibitory antibodies.

FIGS. 1A-1H taken together provide an aligned sequence comparison of the human, pig and mouse factor VIII amino acid sequences. FIG. 1A compares signal peptide regions (human, SEQ ID NO:31; porcine, SEQ ID NO:30, amino acids 1-19; murine, SEQ ID NO:28, amino acids 1-19). Note that the amino acids in FIGS. 1A-1H are numbered at the first Alanine of the mature protein as number 1, with amino acids of the signal peptide assigned negative numbers. The Human fVIII sequence in SEQ ID NO:2 also begins with the first Alanine of the mature protein as amino acid number 1. In the amino acid sequences of mouse fVIII (SEQ ID NO:28) and porcine fVIII (SEQ ID NO:30), the first amino acid (alanine) of the mature sequence is amino acid number 20. FIGS. 1A-1H shows an alignment of the corresponding sequences of human, mouse and pig fVIII, such that the regions of greatest amino acid identity are juxtaposed. The amino acid numbers in FIGS. 1A-1H apply to human fVIII only. FIG. 1B gives the amino acid sequences for the A1 domain of human (SEQ ID NO:2, amino acids 1-372), porcine (SEQ ID NO:30, amino acids 20-391), and murine (SEQ ID NO:28, amino acids 20-391). FIG. 1C provides amino acid sequences for the Factor VIII A2 domains from human (SEQ ID NO:2, amino acids 373-740), pig (SEQ ID NO:30, amino acids 392-759) and mouse (SEQ ID NO:28, amino acids 392-759). FIG. 1D provides the amino acid sequences of B domains of human factor VIII (SEQ ID NO:2, amino acids 741-1648), pig (SEQ ID NO:30, amino acids 760-1449) and mouse (SEQ ID NO:28, amino acids 760-1640). FIG. 1E compares the amino acid sequences of Factor VIII light chain activation peptides of human, pig and mouse (SEQ ID NO:2, amino acids 1649-1689; SEQ ID NO:30, amino acids 1450-1490; and SEQ ID NO:28, amino acids 1641-1678, respectively). FIG. 1F provides the sequence comparison for human, pig and mouse Factor VIII A3 domains (SEQ ID NO:2, amino acids 1690-2019; SEQ ID NO:30, amino acids 1491-1820; and SEQ ID NO:28, amino acids 1679-2006, respectively. FIG. 1G provides the amino acid sequences of the Factor VIII C1 domains of human, pig and mouse (SEQ ID NO:2, amino acids 2020-2172; SEQ ID NO:30, amino acids 1821-1973; and SEQ ID NO:28, amino acids 2007-2159, respectively). FIG. 1 H provides sequence data for the C2 domains of the Factor VIII C2 domains of human, pig and mouse (SEQ ID NO:2, amino acids 2173-2332; SEQ ID NO:30, amino acids 1974-2133; and SEQ ID NO:28, amino acids 2160-2319, respectively).

The diamonds represent tyrosine sulfation sites, proposed binding sites for Factor IXa, phospholipid and Protein C are double-underlined, and regions involved in binding anti-A2 and anti-C2 inhibitory antibodies are italicized. Asterisks highlight amino acid sequences which are conserved. See also SEQ ID NO:29 (porcine factor VIII cDNA) and SEQ ID NO:30 (deduced amino acid sequence of porcine factor VIII). The human numbering system is used as the reference [Wood et al. (1984) supra]. The A1, A2, and B domains are defined by thrombin cleavage sites at positions 372 and 740 and an unknown protease cleavage site at 1648 as residues 1-372, 373-740, and, 741-1648, respectively [Eaton, D. L. et al. (1986) Biochemistry 25:8343-8347]. The A3, C1, and C2 domains are defined as residues 1690-2019, 2020-2172, and 2173-2332, respectively [Vehar et al. (1984) supra]. Cleavage sites for thrombin (factor IIa), factor IXa, factor Xa and APC [Fay et al. (1991) supra; Eaton, D. et al. (1986) Biochemistry 25:505-512; Lamphear, B. J. et al. (1992) Blood 80:3120-3128] are shown by placing the enzyme name over the reactive arginine. An acidic peptide is cleaved from the fVIII light chain by thrombin or factor Xa at position 1689. Proposed binding sites for factor IXa [Fay, P. J. et al. (1994) J. Biol. Chem . 269:20522-20527; Lenting, P. J. et al. (1994) J. Biol. Chem . 269:7150-7155), phospholipid (Foster, P. A. et al. (1990) Blood 75:1999-2004) and protein C (Walker, F. J. et al. (1990) J. Biol. Chem . 265:1484-1489] are doubly underlined. Regions involved in binding anti-A2 [Lubin et al. (1994) supra; Healey et al. (1995) supra]; and previously proposed for anti-C2 inhibitory antibodies are italicized. The C2 inhibitor epitope identified as herein described (human amino acids 2181-2243) is shown by a single underline in FIG. 1 H. Tyrosine sulfation sites [Pittman et al. (1992) supra; Michnick et al. (1994) supra] are shown by ♦.

EXAMPLE 7

Construction of POL1212 and Expression in Baby Hamster Kidney Cells.

POL1212 is a partially B-domainless porcine factor VIII, having the B-domain deleted except that 12 amino acids of the NH2 terminus of the B-domain and 12 amino acids of the —COOH terminus are retained.

The cDNAs encoding for the sequences for the porcine fVIII domains A1, A2, ap-A3-C1, and C2 were obtained as described in Example 5. The DNA nucleotide sequence and derived amino acid sequence of porcine factor VIII are presented as SEQ ID NO:29 and SEQ ID NO:30, respectively. The amplified fragments were separately cloned into the plasmid pBluescript II KS − (pBS).

POL1212 refers to the cDNA encoding porcine fVIII lacking most of the B domain but containing DNA sequence encoding a 24 amino acid linker between the A2 and ap domains. POL1212 was constructed in a mammalian expression vector, ReNeo, which was obtained from Biogen. ReNeo can replicate in bacteria, replicate as an episome in COS cells for transient expression of factor VIII, or be stably integrated into a variety of mammalian cells. It consists of 1) sequences derived from plasmid pBR322 that include an origin of replication and ampicillin resistance gene, 2) a neomycin resistance gene whose expression is under control of the SV40 promoter/enhancer, SV40 small t intron, and the SV40 polyadenylation signal regulatory elements, 3) a site for insertion of fVIII and its signal peptide, the expression of which is under control of the SV40 enhancer, adenovirus type 2 major late promoter, and adenovirus type 2 tripartite leader sequence. Any vector having similar functional components can be used in place of the ReNeo vector.

POL1212/ReNeo was prepared in several steps. First, the cDNAs encoding for porcine fVIII heavy chain (A1-A2) and the cDNAs encoding for porcine fVIII light chain (ap-A3-C1-C2) were separately assembled in pBS. From these constructs, the DNA encoding for porcine B-domainless fVIII was assembled in pBS (PB-/pBS). This form of porcine fVIII lacks the entire B domain, defined as amino acids corresponding to residues 741-1648 in human fVIII (human nucleotides 2278-5001). Next, the DNA encoding for porcine A2 was substituted for the human A2 domain in the human B-domainless fVIII expression vector ReNeo (HB-/ReNeo). The DNA encoding the remainder of the porcine heavy chain and the DNA encoding the porcine light chain was substituted for the human domains in two additional steps using the porcine heavy chain/pBS and PB-/pBS constructs made previously. A fragment of the human B domain encoding the 5 C-terminal and 9 N-terminal amino acids was inserted between the A2 and A3 domains producing a construct called PSQ/ReNeo [Healey et al. (1998)/92:3701-3709]. Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIII). This construct was used as a template to make a fragment of the porcine B domain encoding for the 12 C-terminal and 12 N-terminal amino acids. This fragment was inserted between the A2 and A3 domains resulting in the final construct, POL1212/ReNeo.

The POL1212 24 amino acid linker consists of the first 12 and last 12 residues of the porcine fVIII B domain. The POL1212 linker has the following sequence: SFAQNSRPPSASAPKPPVLRRHQR. (SEQ ID NO:32)

The nucleotide sequence corresponding to the 1212 linker and surrounding amino acids is:

GTC ATT GAA CCT AGG AGC TTT GCC CAG AAT TCA AGA CCC CCT AGT GCG (SEQ ID NO:33)
V   I   E   P   R   S   F   A   Q   N   S   R   P   P   S   A
AGC GCT CCA AAG CCT CCG GTC CTG CGA CGG CAT CAG AGG GAC ATA
S   A   P   K   P   P   V   L   R   R   H   Q   R   D   I
AGC CTT CCT ACT
S   L   P   T

The POL1212 linker was synthesized by splicing-by-overlap extension (SOE) mutagenesis, as follows:

PCR reactions used to make SOE Products were as Follows:

REACTION #1

Outside primer: Rev 4, which is a porcine A2 primer, nucleotides 1742-1761. (SEQ ID NO:29) The sequence is: 5′-GAGGAAAACCAGATGATGTCA-3′ (SEQ ID NO:34)

Inside primer: OL12, which is a porcine reverse primer covering the first (5′) 15 amino acids of OL1212 and the last (3′) 5 amino acids of porcine A2. The sequence is: 5 ′-CTTTGGAGCGCTCGCACTAGGGGGTCTTGAATTCTGGGCAAAGCTCCTAGGTTCAATGAC-3′ (SEQ ID NO:35)

Template: PSQ/ReNeo

Product: porcine DNA from nucleotide 1742 in the A2 domain to 2322 in OL1212, 580 bp

REACTION #2

Outside primer: P2949 is a porcine reverse A3 primer, nucleotides 2998-3021 of SEQ ID NO:29. The sequence is: 5′-GGTCACTTGTCTACCGTGAGCAGC -3′ (see SEQ ID NO:29)

Inside primer: OL12+, a porcine primer covering the last (3′) 16 amino acids of OL1212 and the first (5′) 6 amino acids of the activation peptide, nucleotide 2302-2367 of SEQ ID NO:29. The sequence is: 5′ -CCTAGTGCGAGCGCTCCAAAGCCTCCGGTCCTGCGACGGCATCAGAGGGACATAAGCCTTCCTACT-3′ (SEQ ID NO:36)

Template: PSQ/ReNeo —

Product: porcine from nucleotide 2302 in OL1212 to nucleotide 3021 in the A3 domain, 719 bp

SOE REACTION

Primers: Rev 4, P2949-

Templates: Fragment from rxn #1 (bp) and low melt fragment from rxn #2 (bp)

Product: porcine DNA from nucleotide 1742 in the A2 domain to nucleotide 3021 in the A3 domain (SEQ ID NO:29) including OL1212, 1279 bp. The reaction product was ethanol precipitated.

The 1212 linker was inserted into PSQ/ReNeo by cutting the SOE product (insert) and PSQ/ReNeo (vector) with BsaB I. The vector and insert were ligated using T4 ligase and the product was used to transform E. coli XL1-Blue cells. Plasmid DNA was prepared from several colonies and the sequence of the 1212 linker and other PCR-generated sequence was verified by DNA sequence analysis.

CULTURE OF BABY HAMSTER KIDNEY (BHK) CRL-1632 CELLS

A BHK cell line was obtained from the ATCC, accession identification CRL-1632 and was stored frozen at −20° C. until further use. The cells were thawed at 37° C. and put into 10 ml of complete medium, defined as DMEM/F12, 50 U/ml penicillin, 50 μg/ml streptomycin plus 10% fetal bovine serum (FBS). FBS was purchased from Hyclone, Logan Utah. The cells were centrifuged for 2 minutes at 300 RPM. The medium was aspirated and the cells were resuspended in two ml complete medium in a T-75 flask containing 20 ml of complete medium.

POL1212 has been expressed in both baby hamster kidney (BHK) and Chinese hamster ovary (CHO) cells. Two BHK lines were used, the CRL-1632 line from ATCC and another BHK line obtained from R. Mcgillivray, University of British Columbia, [Funk, et al. (1990) Biochemistry 29:1654-1660]. The latter were subcultured without selection in the inventors lab and designated BHK1632 (Emory). The CHO cell line was CHO-K1, ATCC accession CCL-61. The expression of the average clone from the Emory cell line and from CHO-K1 cells was somewhat higher than from CRL-1632 cells as judged by chromogenic assay activity.

The cells grown in the T-75 flask formed a confluent monolayer. A 60 ml culture of E. coli XL1-Blue cells in LB/ampicillin (50 mg/mi) carrying the POL1212/ReNeo plasmid was prepared.

TRANSFECTION OF CRL-1632 BHK CELLS WITH POL1212/ReNeo

DNA from the overnight culture of the POL1212/ReNeo XL1-Blue cells was prepared using a Qiagen, Valencia, Calif. Spin Miniprep kit. One flask of CRL-1632 cells was split into a stock flask with 0.2 ml and a flask for transfection with 0.3 ml from 2 ml total. The other flask was fed fresh medium. Medium was DMEM/F12+10% Hyclone FBS+50 U/ml penicillin, 50 μg/ml streptomycin. CRL-1632 cells were split into 6 well plates aiming for 50-90% confluence for transfection (0.3 ml of cells from the T-75 flask in 2 ml 1:5000 Versene [Life Technologies, Gaithersburg, Md.] in each well) using fresh DMEM/F12+10% Hyclone FBS+50 U/ml penicillin, 50 μg/ml streptomycin.

The following solutions were prepared in sterile 1-2 ml test tubes;

A) 48 μl (10 μg) Miniprep POL1212/ReNeo DNA plus μl medium without serum (DMEM/F12) plus 10 μl Lipofectin™ (Life Technologies, Gaithersburg, Md.).

B) 10 μl Lipofectin plus 190 μl medium (mock transfection) was gently mixed and the DNA and Lipofectin allowed to react for 15 minutes at room temperature. During this time, the cells were washed twice with 2 ml of DMEM/F12. 1.8 ml of DMEM/F12 was then added to the cells. The DNA/Lipofectin complex was added dropwise to the cells, and swirled gently to mix. The cells remained in the incubator overnight. Removed the DNA/Lipofectin and added 3 ml of medium with serum to the cells. Incubated the cells 30-48 hours. Geneticin was purchased from Life Technologies, Gaithersburg, Md. The cell cultures were divided 1:20, 1:50 and 1:100, 1:250, 1:500 onto 10 cm dishes in 10 ml of medium with serum containing 535 μg/ml geneticin. Over the next several days, cells that did not take up the POL1212/ReNeo plasmid were killed due to the presence of geneticin. The remaining cells continued to replicate in geneticin, forming visible monolayer colonies on the dishes.

EXPRESSION AND ASSAY OF POL1212 from BHK CRL-1632 CELLS

Small plastic cylindrical rings were placed around the colonies. The colonies were aspirated separately using complete medium and transferred to test tubes. These colonies are referred to as ring cloned colonies. Ring cloned colonies were plated separately onto 24 well plates and grown in complete medium.

CHROMOGENIC SUBSTRATE ASSAY FOR FACTOR VIII EXPRESSION BY TRANSFECTED CRL-1632 CELLS

Samples of POL1212 from cell culture supernatants were mixed with 50 nM purified porcine factor IXa and 0,05 mM phosphtidylcholine/phosphatidylserine (PCPS) vesicles in 0. 15M NaCl, 20 m HEPES, 5mM CaCl2, 0.01% Tween 80, pH 7.4. As a control, cell culture medium from mock-transfected cells was used. Thrombin and factor X were added simultaneously to final concentrations of 40 and 425 nM, respectively. thrombin activates factor VIII, which then, along with PCPS, serves as a cofactor for factor IXa during the activation of factor X.

After 5 min, the activation of factor X by factor IXa/factor VIIIa/PCPS was stopped by the addition of EDTA to a final concentration of 50 mM. At the same time the activation of factor VIII by thrombin was stopped by the addition of the thrombin inhibitor, recombinant desulfatohirudin, to a final concentration of 100 nM. A 25-μl sample of the reaction mix was transferred to a microtiter well, to which was added 74 μl of Spectrozyme Xa (America Diagnostica, Greenwich, Conn.), which is a chromogenic substrate for factor Xa. The final concentration of Spectrozyme Xa was 0.6 mM. The absorbance at 405 nm due to the cleavage of Spectrozyme Xa by factor Xa was monitored continuously for 5 minutes with a Vmax Kinetic Plate Reader (Molecular Devices, Inc., Menlo park, Calif.). The results are expressed in terms of A405/min.

Factor VIII chromogenic assay of ten ring-cloned colonies:

Colony number A                                                                        405                                                                    /min (× 10                                                                        3                                                                    )
Buffer        0.2
1             2.1
2             8.4
3             6.4
4             10.7
5             12.5
6             7.6
7             51.3
8             139.5
9             3.8
10            8.4

These results show that all ten colonies that were selected express factor VIII activity that is at least ten-fold greater than background.

The activity from medium of colony 8, which was the highest expressing colony, was further examined by one-state factor VIII clotting assay. In this assay, 50 ml of factor VIII deficient plasma (George King Biomedical Overland Park, Kans.), 5 ml sample or standard, and 50 ml of activated particulate thromboplastin time reagent (Organon Teknika, Durham, N.C.) were incubated 3 min at 37° C. Samples include colony 8 medium diluted in 0.15 M NaCl, mM hepes, pH 7.4 (HBS) or, as a control, complete medium. Clotting was initiated by addition of 50 ml of 20 mM CaCl2. The clotting time was measured using an ST4 BIO Coagulation Instrument (Diagnostica Stago, Parsippany, N.J.). A standard curve was obtained by making dilutions of pooled, citrated normal human plasma, lot 0641 (George King Biomedical, Overland Park, Kans.). The factor VIII concentration of the standard was 0.9 units per ml.

Standard Curve:

	Dilution	U/ml	Clot Time
1)	Undiluted	0.96	45.2
2)	1/3 (HBS)	0.32	53.7
3)	1/11 (HBS)	0.087	62.5
4)	1/21 (HBS)	0.046	68.9

Linear regression of the clotting times versus the logarithm of the concentration of standard yielded a correlation coefficient of 0.997.

Test substances gave the following clotting times, which were converted to units per ml using the standard curve:

	Sample	Clot Time (sec)	Units/ml
1)	Colony 8 (24 h), 1/10 in HBS	40.6	1.74 × 10 = 17.4
2)	Colony 8 (24 h), 1/10 in HBS	41.1	1.63 × 10 = 16.3
3)	Colony 8 (24 h), 1/20 in HBS	47.7	0.69 × 20 = 13.8
4)	Colony 8 (24 h), 1/20 in HBS	47.2	0.73 × 20 = 14.6
5)	Complete medium	82.9	0.007
6)	Complete medium	83.3	0.006

These results show that colony 8 clotting activity that is approximately 2000-fold higher than the control sample.

The DNA sequence encoding POL1212 is set forth as SEQ ID NO:37. The encoded amino acid sequence of POL1212 is set forth as SEQ ID NO:38. Further purification of POL1212 can be carried out using a variety of known methods such as immunoaffinity chromatography and HPLC chromatography—see Examples 2 and 3.

GENERAL CONCLUDING REMARKS

It will be understood that minor variations of amino acid sequence or the DNA encoding such sequence relating to POL1212 can be introduced without affecting the essential attributes of function. For example, the length of B-domain sequence retained as a linker between the A2 domain and the activation peptide can be increased or decreased within limits known in the art. Sequence variants can be introduced in the linker region while retaining the equivalent functional attributes of POL1212 as taught herein and of porcine B-domainless factor VIII as taught herein and as known in the art. Based on comparisons of known factor VIII amino acid sequences having coagulant activity in human blood, sequence variants such as individual amino acid substitutions or substitution of peptide segments with known functional variants can be made in the basic POL1212 amino acid sequence, while retaining the equivalent functional attributes thereof. The foregoing types of variation are not intended as exhaustive, but are merely exemplary of the sequence modifications that could be made by those of ordinary skill in the art, without substantially modifying the functional attributes of the protein. All such variants and modifications are deemed to fall within the scope of the invention as claimed or as equivalents thereof.

Sequence ID Listing

SEQ ID NO: Identification
1          Human factor VIII cDNA. Coding for amino acid number 1
           of the mature protein begins at nucleotide number 208.
2          Human factor amino acid sequence.
3          Porcine factor VIII A2 domain cDNA
4          Porcine factor VIII A2 domain amino acid sequence
5 thru 27  Oligonucleotide primer seq. (Example 5)
28         Murine factor VIII amino acid sequence
29         Porcine factor VIII cDNA
30         Porcine factor VIII amino acid sequence
31         Human factor VIII signal peptide amino acid sequence
32 thru 36 Oligonucleotiode primer (Example 7)
37         POL1212 coding DNA
38         POL1212 amino acid sequence

The BHK 1632 (Emory) cell line was deposited with the American Type Culture Collection, 10801 University Blvd., Manassas, VA, 20110-2209, under the designation BHK-M on Jun. 27, 2002 (Deposited as PTA-4506).

38 1 9009 DNA Homo sapiens CDS (208)..(7203) 1cagtgggtaa gttccttaaa tgctctgcaa agaaattggg acttttcatt aaatcagaaa 60ttttactttt ttcccctcct gggagctaaa gatattttag agaagaatta accttttgct 120tctccagttg aacatttgta gcaataagtc atgcaaatag agctctccac ctgcttcttt 180ctgtgccttt tgcgattctg ctttagt gcc acc aga aga tac tac ctg ggt gca 234 Ala Thr Arg Arg Tyr Tyr Leu Gly Ala 1 5gtg gaa ctg tca tgg gac tat atg caa agt gat ctc ggt gag ctg cct 282Val Glu Leu Ser Trp Asp Tyr Met Gln Ser Asp Leu Gly Glu Leu Pro 10 15 20 25gtg gac gca aga ttt cct cct aga gtg cca aaa tct ttt cca ttc aac 330Val Asp Ala Arg Phe Pro Pro Arg Val Pro Lys Ser Phe Pro Phe Asn 30 35 40acc tca gtc gtg tac aaa aag act ctg ttt gta gaa ttc acg gtt cac 378Thr Ser Val Val Tyr Lys Lys Thr Leu Phe Val Glu Phe Thr Val His 45 50 55ctt ttc aac atc gct aag cca agg cca ccc tgg atg ggt ctg cta ggt 426Leu Phe Asn Ile Ala Lys Pro Arg Pro Pro Trp Met Gly Leu Leu Gly 60 65 70cct acc atc cag gct gag gtt tat gat aca gtg gtc att aca ctt aag 474Pro Thr Ile Gln Ala Glu Val Tyr Asp Thr Val Val Ile Thr Leu Lys 75 80 85aac atg gct tcc cat cct gtc agt ctt cat gct gtt ggt gta tcc tac 522Asn Met Ala Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Tyr 90 95 100 105tgg aaa gct tct gag gga gct gaa tat gat gat cag acc agt caa agg 570Trp Lys Ala Ser Glu Gly Ala Glu Tyr Asp Asp Gln Thr Ser Gln Arg 110 115 120gag aaa gaa gat gat aaa gtc ttc cct ggt gga agc cat aca tat gtc 618Glu Lys Glu Asp Asp Lys Val Phe Pro Gly Gly Ser His Thr Tyr Val 125 130 135tgg cag gtc ctg aaa gag aat ggt cca atg gcc tct gac cca ctg tgc 666Trp Gln Val Leu Lys Glu Asn Gly Pro Met Ala Ser Asp Pro Leu Cys 140 145 150ctt acc tac tca tat ctt tct cat gtg gac ctg gta aaa gac ttg aat 714Leu Thr Tyr Ser Tyr Leu Ser His Val Asp Leu Val Lys Asp Leu Asn 155 160 165tca ggc ctc att gga gcc cta cta gta tgt aga gaa ggg agt ctg gcc 762Ser Gly Leu Ile Gly Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Ala170 175 180 185aag gaa aag aca cag acc ttg cac aaa ttt ata cta ctt ttt gct gta 810Lys Glu Lys Thr Gln Thr Leu His Lys Phe Ile Leu Leu Phe Ala Val 190 195 200ttt gat gaa ggg aaa agt tgg cac tca gaa aca aag aac tcc ttg atg 858Phe Asp Glu Gly Lys Ser Trp His Ser Glu Thr Lys Asn Ser Leu Met 205 210 215cag gat agg gat gct gca tct gct cgg gcc tgg cct aaa atg cac aca 906Gln Asp Arg Asp Ala Ala Ser Ala Arg Ala Trp Pro Lys Met His Thr 220 225 230gtc aat ggt tat gta aac agg tct ctg cca ggt ctg att gga tgc cac 954Val Asn Gly Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His 235 240 245agg aaa tca gtc tat tgg cat gtg att gga atg ggc acc act cct gaa 1002Arg Lys Ser Val Tyr Trp His Val Ile Gly Met Gly Thr Thr Pro Glu250 255 260 265gtg cac tca ata ttc ctc gaa ggt cac aca ttt ctt gtg agg aac cat 1050Val His Ser Ile Phe Leu Glu Gly His Thr Phe Leu Val Arg Asn His 270 275 280cgc cag gcg tcc ttg gaa atc tcg cca ata act ttc ctt act gct caa 1098Arg Gln Ala Ser Leu Glu Ile Ser Pro Ile Thr Phe Leu Thr Ala Gln 285 290 295aca ctc ttg atg gac ctt gga cag ttt cta ctg ttt tgt cat atc tct 1146Thr Leu Leu Met Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser 300 305 310tcc cac caa cat gat ggc atg gaa gct tat gtc aaa gta gac agc tgt 1194Ser His Gln His Asp Gly Met Glu Ala Tyr Val Lys Val Asp Ser Cys 315 320 325cca gag gaa ccc caa cta cga atg aaa aat aat gaa gaa gcg gaa gac 1242Pro Glu Glu Pro Gln Leu Arg Met Lys Asn Asn Glu Glu Ala Glu Asp330 335 340 345tat gat gat gat ctt act gat tct gaa atg gat gtg gtc agg ttt gat 1290Tyr Asp Asp Asp Leu Thr Asp Ser Glu Met Asp Val Val Arg Phe Asp 350 355 360gat gac aac tct cct tcc ttt atc caa att cgc tca gtt gcc aag aag 1338Asp Asp Asn Ser Pro Ser Phe Ile Gln Ile Arg Ser Val Ala Lys Lys 365 370 375cat cct aaa act tgg gta cat tac att gct gct gaa gag gag gac tgg 1386His Pro Lys Thr Trp Val His Tyr Ile Ala Ala Glu Glu Glu Asp Trp 380 385 390gac tat gct ccc tta gtc ctc gcc ccc gat gac aga agt tat aaa agt 1434Asp Tyr Ala Pro Leu Val Leu Ala Pro Asp Asp Arg Ser Tyr Lys Ser 395 400 405caa tat ttg aac aat ggc cct cag cgg att ggt agg aag tac aaa aaa 1482Gln Tyr Leu Asn Asn Gly Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys410 415 420 425gtc cga ttt atg gca tac aca gat gaa acc ttt aag act cgt gaa gct 1530Val Arg Phe Met Ala Tyr Thr Asp Glu Thr Phe Lys Thr Arg Glu Ala 430 435 440att cag cat gaa tca gga atc ttg gga cct tta ctt tat ggg gaa gtt 1578Ile Gln His Glu Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val 445 450 455gga gac aca ctg ttg att ata ttt aag aat caa gca agc aga cca tat 1626Gly Asp Thr Leu Leu Ile Ile Phe Lys Asn Gln Ala Ser Arg Pro Tyr 460 465 470aac atc tac cct cac gga atc act gat gtc cgt cct ttg tat tca agg 1674Asn Ile Tyr Pro His Gly Ile Thr Asp Val Arg Pro Leu Tyr Ser Arg 475 480 485aga tta cca aaa ggt gta aaa cat ttg aag gat ttt cca att ctg cca 1722Arg Leu Pro Lys Gly Val Lys His Leu Lys Asp Phe Pro Ile Leu Pro490 495 500 505gga gaa ata ttc aaa tat aaa tgg aca gtg act gta gaa gat ggg cca 1770Gly Glu Ile Phe Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly Pro 510 515 520act aaa tca gat cct cgg tgc ctg acc cgc tat tac tct agt ttc gtt 1818Thr Lys Ser Asp Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Phe Val 525 530 535aat atg gag aga gat cta gct tca gga ctc att ggc cct ctc ctc atc 1866Asn Met Glu Arg Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile 540 545 550tgc tac aaa gaa tct gta gat caa aga gga aac cag ata atg tca gac 1914Cys Tyr Lys Glu Ser Val Asp Gln Arg Gly Asn Gln Ile Met Ser Asp 555 560 565aag agg aat gtc atc ctg ttt tct gta ttt gat gag aac cga agc tgg 1962Lys Arg Asn Val Ile Leu Phe Ser Val Phe Asp Glu Asn Arg Ser Trp570 575 580 585tac ctc aca gag aat ata caa cgc ttt ctc ccc aat cca gct gga gtg 2010Tyr Leu Thr Glu Asn Ile Gln Arg Phe Leu Pro Asn Pro Ala Gly Val 590 595 600cag ctt gag gat cca gag ttc caa gcc tcc aac atc atg cac agc atc 2058Gln Leu Glu Asp Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile 605 610 615aat ggc tat gtt ttt gat agt ttg cag ttg tca gtt tgt ttg cat gag 2106Asn Gly Tyr Val Phe Asp Ser Leu Gln Leu Ser Val Cys Leu His Glu 620 625 630gtg gca tac tgg tac att cta agc att gga gca cag act gac ttc ctt 2154Val Ala Tyr Trp Tyr Ile Leu Ser Ile Gly Ala Gln Thr Asp Phe Leu 635 640 645tct gtc ttc ttc tct gga tat acc ttc aaa cac aaa atg gtc tat gaa 2202Ser Val Phe Phe Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu650 655 660 665gac aca ctc acc cta ttc cca ttc tca gga gaa act gtc ttc atg tcg 2250Asp Thr Leu Thr Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser 670 675 680atg gaa aac cca ggt cta tgg att ctg ggg tgc cac aac tca gac ttt 2298Met Glu Asn Pro Gly Leu Trp Ile Leu Gly Cys His Asn Ser Asp Phe 685 690 695cgg aac aga ggc atg acc gcc tta ctg aag gtt tct agt tgt gac aag 2346Arg Asn Arg Gly Met Thr Ala Leu Leu Lys Val Ser Ser Cys Asp Lys 700 705 710aac act ggt gat tat tac gag gac agt tat gaa gat att tca gca tac 2394Asn Thr Gly Asp Tyr Tyr Glu Asp Ser Tyr Glu Asp Ile Ser Ala Tyr 715 720 725ttg ctg agt aaa aac aat gcc att gaa cca aga agc ttc tcc cag aat 2442Leu Leu Ser Lys Asn Asn Ala Ile Glu Pro Arg Ser Phe Ser Gln Asn730 735 740 745tca aga cac cct agc act agg caa aag caa ttt aat gcc acc aca att 2490Ser Arg His Pro Ser Thr Arg Gln Lys Gln Phe Asn Ala Thr Thr Ile 750 755 760cca gaa aat gac ata gag aag act gac cct tgg ttt gca cac aga aca 2538Pro Glu Asn Asp Ile Glu Lys Thr Asp Pro Trp Phe Ala His Arg Thr 765 770 775cct atg cct aaa ata caa aat gtc tcc tct agt gat ttg ttg atg ctc 2586Pro Met Pro Lys Ile Gln Asn Val Ser Ser Ser Asp Leu Leu Met Leu 780 785 790ttg cga cag agt cct act cca cat ggg cta tcc tta tct gat ctc caa 2634Leu Arg Gln Ser Pro Thr Pro His Gly Leu Ser Leu Ser Asp Leu Gln 795 800 805gaa gcc aaa tat gag act ttt tct gat gat cca tca cct gga gca ata 2682Glu Ala Lys Tyr Glu Thr Phe Ser Asp Asp Pro Ser Pro Gly Ala Ile810 815 820 825gac agt aat aac agc ctg tct gaa atg aca cac ttc agg cca cag ctc 2730Asp Ser Asn Asn Ser Leu Ser Glu Met Thr His Phe Arg Pro Gln Leu 830 835 840cat cac agt ggg gac atg gta ttt acc cct gag tca ggc ctc caa tta 2778His His Ser Gly Asp Met Val Phe Thr Pro Glu Ser Gly Leu Gln Leu 845 850 855aga tta aat gag aaa ctg ggg aca act gca gca aca gag ttg aag aaa 2826Arg Leu Asn Glu Lys Leu Gly Thr Thr Ala Ala Thr Glu Leu Lys Lys 860 865 870ctt gat ttc aaa gtt tct agt aca tca aat aat ctg att tca aca att 2874Leu Asp Phe Lys Val Ser Ser Thr Ser Asn Asn Leu Ile Ser Thr Ile 875 880 885cca tca gac aat ttg gca gca ggt act gat aat aca agt tcc tta gga 2922Pro Ser Asp Asn Leu Ala Ala Gly Thr Asp Asn Thr Ser Ser Leu Gly890 895 900 905ccc cca agt atg cca gtt cat tat gat agt caa tta gat acc act cta 2970Pro Pro Ser Met Pro Val His Tyr Asp Ser Gln Leu Asp Thr Thr Leu 910 915 920ttt ggc aaa aag tca tct ccc ctt act gag tct ggt gga cct ctg agc 3018Phe Gly Lys Lys Ser Ser Pro Leu Thr Glu Ser Gly Gly Pro Leu Ser 925 930 935ttg agt gaa gaa aat aat gat tca aag ttg tta gaa tca ggt tta atg 3066Leu Ser Glu Glu Asn Asn Asp Ser Lys Leu Leu Glu Ser Gly Leu Met 940 945 950aat agc caa gaa agt tca tgg gga aaa aat gta tcg tca aca gag agt 3114Asn Ser Gln Glu Ser Ser Trp Gly Lys Asn Val Ser Ser Thr Glu Ser 955 960 965ggt agg tta ttt aaa ggg aaa aga gct cat gga cct gct ttg ttg act 3162Gly Arg Leu Phe Lys Gly Lys Arg Ala His Gly Pro Ala Leu Leu Thr970 975 980 985aaa gat aat gcc tta ttc aaa gtt agc atc tct ttg tta aag aca aac 3210Lys Asp Asn Ala Leu Phe Lys Val Ser Ile Ser Leu Leu Lys Thr Asn 990 995 1000aaa act tcc aat aat tca gca act aat aga aag act cac att gat ggc 3258Lys Thr Ser Asn Asn Ser Ala Thr Asn Arg Lys Thr His Ile Asp Gly 1005 1010 1015cca tca tta tta att gag aat agt cca tca gtc tgg caa aat ata tta 3306Pro Ser Leu Leu Ile Glu Asn Ser Pro Ser Val Trp Gln Asn Ile Leu 1020 1025 1030gaa agt gac act gag ttt aaa aaa gtg aca cct ttg att cat gac aga 3354Glu Ser Asp Thr Glu Phe Lys Lys Val Thr Pro Leu Ile His Asp Arg 1035 1040 1045atg ctt atg gac aaa aat gct aca gct ttg agg cta aat cat atg tca 3402Met Leu Met Asp Lys Asn Ala Thr Ala Leu Arg Leu Asn His Met Ser1050 1055 1060 1065aat aaa act act tca tca aaa aac atg gaa atg gtc caa cag aaa aaa 3450Asn Lys Thr Thr Ser Ser Lys Asn Met Glu Met Val Gln Gln Lys Lys 1070 1075 1080gag ggc ccc att cca cca gat gca caa aat cca gat atg tcg ttc ttt 3498Glu Gly Pro Ile Pro Pro Asp Ala Gln Asn Pro Asp Met Ser Phe Phe 1085 1090 1095aag atg cta ttc ttg cca gaa tca gca agg tgg ata caa agg act cat 3546Lys Met Leu Phe Leu Pro Glu Ser Ala Arg Trp Ile Gln Arg Thr His 1100 1105 1110gga aag aac tct ctg aac tct ggg caa ggc ccc agt cca aag caa tta 3594Gly Lys Asn Ser Leu Asn Ser Gly Gln Gly Pro Ser Pro Lys Gln Leu 1115 1120 1125gta tcc tta gga cca gaa aaa tct gtg gaa ggt cag aat ttc ttg tct 3642Val Ser Leu Gly Pro Glu Lys Ser Val Glu Gly Gln Asn Phe Leu Ser1130 1135 1140 1145gag aaa aac aaa gtg gta gta gga aag ggt gaa ttt aca aag gac gta 3690Glu Lys Asn Lys Val Val Val Gly Lys Gly Glu Phe Thr Lys Asp Val 1150 1155 1160gga ctc aaa gag atg gtt ttt cca agc agc aga aac cta ttt ctt act 3738Gly Leu Lys Glu Met Val Phe Pro Ser Ser Arg Asn Leu Phe Leu Thr 1165 1170 1175aac ttg gat aat tta cat gaa aat aat aca cac aat caa gaa aaa aaa 3786Asn Leu Asp Asn Leu His Glu Asn Asn Thr His Asn Gln Glu Lys Lys 1180 1185 1190att cag gaa gaa ata gaa aag aag gaa aca tta atc caa gag aat gta 3834Ile Gln Glu Glu Ile Glu Lys Lys Glu Thr Leu Ile Gln Glu Asn Val 1195 1200 1205gtt ttg cct cag ata cat aca gtg act ggc act aag aat ttc atg aag 3882Val Leu Pro Gln Ile His Thr Val Thr Gly Thr Lys Asn Phe Met Lys1210 1215 1220 1225aac ctt ttc tta ctg agc act agg caa aat gta gaa ggt tca tat gag 3930Asn Leu Phe Leu Leu Ser Thr Arg Gln Asn Val Glu Gly Ser Tyr Glu 1230 1235 1240ggg gca tat gct cca gta ctt caa gat ttt agg tca tta aat gat tca 3978Gly Ala Tyr Ala Pro Val Leu Gln Asp Phe Arg Ser Leu Asn Asp Ser 1245 1250 1255aca aat aga aca aag aaa cac aca gct cat ttc tca aaa aaa ggg gag 4026Thr Asn Arg Thr Lys Lys His Thr Ala His Phe Ser Lys Lys Gly Glu 1260 1265 1270gaa gaa aac ttg gaa ggc ttg gga aat caa acc aag caa att gta gag 4074Glu Glu Asn Leu Glu Gly Leu Gly Asn Gln Thr Lys Gln Ile Val Glu 1275 1280 1285aaa tat gca tgc acc aca agg ata tct cct aat aca agc cag cag aat 4122Lys Tyr Ala Cys Thr Thr Arg Ile Ser Pro Asn Thr Ser Gln Gln Asn1290 1295 1300 1305ttt gtc acg caa cgt agt aag aga gct ttg aaa caa ttc aga ctc cca 4170Phe Val Thr Gln Arg Ser Lys Arg Ala Leu Lys Gln Phe Arg Leu Pro 1310 1315 1320cta gaa gaa aca gaa ctt gaa aaa agg ata att gtg gat gac acc tca 4218Leu Glu Glu Thr Glu Leu Glu Lys Arg Ile Ile Val Asp Asp Thr Ser 1325 1330 1335acc cag tgg tcc aaa aac atg aaa cat ttg acc ccg agc acc ctc aca 4266Thr Gln Trp Ser Lys Asn Met Lys His Leu Thr Pro Ser Thr Leu Thr 1340 1345 1350cag ata gac tac aat gag aag gag aaa ggg gcc att act cag tct ccc 4314Gln Ile Asp Tyr Asn Glu Lys Glu Lys Gly Ala Ile Thr Gln Ser Pro 1355 1360 1365tta tca gat tgc ctt acg agg agt cat agc atc cct caa gca aat aga 4362Leu Ser Asp Cys Leu Thr Arg Ser His Ser Ile Pro Gln Ala Asn Arg1370 1375 1380 1385tct cca tta ccc att gca aag gta tca tca ttt cca tct att aga cct 4410Ser Pro Leu Pro Ile Ala Lys Val Ser Ser Phe Pro Ser Ile Arg Pro 1390 1395 1400ata tat ctg acc agg gtc cta ttc caa gac aac tct tct cat ctt cca 4458Ile Tyr Leu Thr Arg Val Leu Phe Gln Asp Asn Ser Ser His Leu Pro 1405 1410 1415gca gca tct tat aga aag aaa gat tct ggg gtc caa gaa agc agt cat 4506Ala Ala Ser Tyr Arg Lys Lys Asp Ser Gly Val Gln Glu Ser Ser His 1420 1425 1430ttc tta caa gga gcc aaa aaa aat aac ctt tct tta gcc att cta acc 4554Phe Leu Gln Gly Ala Lys Lys Asn Asn Leu Ser Leu Ala Ile Leu Thr 1435 1440 1445ttg gag atg act ggt gat caa aga gag gtt ggc tcc ctg ggg aca agt 4602Leu Glu Met Thr Gly Asp Gln Arg Glu Val Gly Ser Leu Gly Thr Ser1450 1455 1460 1465gcc aca aat tca gtc aca tac aag aaa gtt gag aac act gtt ctc ccg 4650Ala Thr Asn Ser Val Thr Tyr Lys Lys Val Glu Asn Thr Val Leu Pro 1470 1475 1480aaa cca gac ttg ccc aaa aca tct ggc aaa gtt gaa ttg ctt cca aaa 4698Lys Pro Asp Leu Pro Lys Thr Ser Gly Lys Val Glu Leu Leu Pro Lys 1485 1490 1495gtt cac att tat cag aag gac cta ttc cct acg gaa act agc aat ggg 4746Val His Ile Tyr Gln Lys Asp Leu Phe Pro Thr Glu Thr Ser Asn Gly 1500 1505 1510tct cct ggc cat ctg gat ctc gtg gaa ggg agc ctt ctt cag gga aca 4794Ser Pro Gly His Leu Asp Leu Val Glu Gly Ser Leu Leu Gln Gly Thr 1515 1520 1525gag gga gcg att aag tgg aat gaa gca aac aga cct gga aaa gtt ccc 4842Glu Gly Ala Ile Lys Trp Asn Glu Ala Asn Arg Pro Gly Lys Val Pro1530 1535 1540 1545ttt ctg aga gta gca aca gaa agc tct gca aag act ccc tcc aag cta 4890Phe Leu Arg Val Ala Thr Glu Ser Ser Ala Lys Thr Pro Ser Lys Leu 1550 1555 1560ttg gat cct ctt gct tgg gat aac cac tat ggt act cag ata cca aaa 4938Leu Asp Pro Leu Ala Trp Asp Asn His Tyr Gly Thr Gln Ile Pro Lys 1565 1570 1575gaa gag tgg aaa tcc caa gag aag tca cca gaa aaa aca gct ttt aag 4986Glu Glu Trp Lys Ser Gln Glu Lys Ser Pro Glu Lys Thr Ala Phe Lys 1580 1585 1590aaa aag gat acc att ttg tcc ctg aac gct tgt gaa agc aat cat gca 5034Lys Lys Asp Thr Ile Leu Ser Leu Asn Ala Cys Glu Ser Asn His Ala 1595 1600 1605ata gca gca ata aat gag gga caa aat aag ccc gaa ata gaa gtc acc 5082Ile Ala Ala Ile Asn Glu Gly Gln Asn Lys Pro Glu Ile Glu Val Thr1610 1615 1620 1625tgg gca aag caa ggt agg act gaa agg ctg tgc tct caa aac cca cca 5130Trp Ala Lys Gln Gly Arg Thr Glu Arg Leu Cys Ser Gln Asn Pro Pro 1630 1635 1640gtc ttg aaa cgc cat caa cgg gaa ata act cgt act act ctt cag tca 5178Val Leu Lys Arg His Gln Arg Glu Ile Thr Arg Thr Thr Leu Gln Ser 1645 1650 1655gat caa gag gaa att gac tat gat gat acc ata tca gtt gaa atg aag 5226Asp Gln Glu Glu Ile Asp Tyr Asp Asp Thr Ile Ser Val Glu Met Lys 1660 1665 1670aag gaa gat ttt gac att tat gat gag gat gaa aat cag agc ccc cgc 5274Lys Glu Asp Phe Asp Ile Tyr Asp Glu Asp Glu Asn Gln Ser Pro Arg 1675 1680 1685agc ttt caa aag aaa aca cga cac tat ttt att gct gca gtg gag agg 5322Ser Phe Gln Lys Lys Thr Arg His Tyr Phe Ile Ala Ala Val Glu Arg1690 1695 1700 1705ctc tgg gat tat ggg atg agt agc tcc cca cat gtt cta aga aac agg 5370Leu Trp Asp Tyr Gly Met Ser Ser Ser Pro His Val Leu Arg Asn Arg 1710 1715 1720gct cag agt ggc agt gtc cct cag ttc aag aaa gtt gtt ttc cag gaa 5418Ala Gln Ser Gly Ser Val Pro Gln Phe Lys Lys Val Val Phe Gln Glu 1725 1730 1735ttt act gat ggc tcc ttt act cag ccc tta tac cgt gga gaa cta aat 5466Phe Thr Asp Gly Ser Phe Thr Gln Pro Leu Tyr Arg Gly Glu Leu Asn 1740 1745 1750gaa cat ttg gga ctc ctg ggg cca tat ata aga gca gaa gtt gaa gat 5514Glu His Leu Gly Leu Leu Gly Pro Tyr Ile Arg Ala Glu Val Glu Asp 1755 1760 1765aat atc atg gta act ttc aga aat cag gcc tct cgt ccc tat tcc ttc 5562Asn Ile Met Val Thr Phe Arg Asn Gln Ala Ser Arg Pro Tyr Ser Phe1770 1775 1780 1785tat tct agc ctt att tct tat gag gaa gat cag agg caa gga gca gaa 5610Tyr Ser Ser Leu Ile Ser Tyr Glu Glu Asp Gln Arg Gln Gly Ala Glu 1790 1795 1800cct aga aaa aac ttt gtc aag cct aat gaa acc aaa act tac ttt tgg 5658Pro Arg Lys Asn Phe Val Lys Pro Asn Glu Thr Lys Thr Tyr Phe Trp 1805 1810 1815aaa gtg caa cat cat atg gca ccc act aaa gat gag ttt gac tgc aaa 5706Lys Val Gln His His Met Ala Pro Thr Lys Asp Glu Phe Asp Cys Lys 1820 1825 1830gcc tgg gct tat ttc tct gat gtt gac ctg gaa aaa gat gtg cac tca 5754Ala Trp Ala Tyr Phe Ser Asp Val Asp Leu Glu Lys Asp Val His Ser 1835 1840 1845ggc ctg att gga ccc ctt ctg gtc tgc cac act aac aca ctg aac cct 5802Gly Leu Ile Gly Pro Leu Leu Val Cys His Thr Asn Thr Leu Asn Pro1850 1855 1860 1865gct cat ggg aga caa gtg aca gta cag gaa ttt gct ctg ttt ttc acc 5850Ala His Gly Arg Gln Val Thr Val Gln Glu Phe Ala Leu Phe Phe Thr 1870 1875 1880atc ttt gat gag acc aaa agc tgg tac ttc act gaa aat atg gaa aga 5898Ile Phe Asp Glu Thr Lys Ser Trp Tyr Phe Thr Glu Asn Met Glu Arg 1885 1890 1895aac tgc agg gct ccc tgc aat atc cag atg gaa gat ccc act ttt aaa 5946Asn Cys Arg Ala Pro Cys Asn Ile Gln Met Glu Asp Pro Thr Phe Lys 1900 1905 1910gag aat tat cgc ttc cat gca atc aat ggc tac ata atg gat aca cta 5994Glu Asn Tyr Arg Phe His Ala Ile Asn Gly Tyr Ile Met Asp Thr Leu 1915 1920 1925cct ggc tta gta atg gct cag gat caa agg att cga tgg tat ctg ctc 6042Pro Gly Leu Val Met Ala Gln Asp Gln Arg Ile Arg Trp Tyr Leu Leu1930 1935 1940 1945agc atg ggc agc aat gaa aac atc cat tct att cat ttc agt gga cat 6090Ser Met Gly Ser Asn Glu Asn Ile His Ser Ile His Phe Ser Gly His 1950 1955 1960gtg ttc act gta cga aaa aaa gag gag tat aaa atg gca ctg tac aat 6138Val Phe Thr Val Arg Lys Lys Glu Glu Tyr Lys Met Ala Leu Tyr Asn 1965 1970 1975ctc tat cca ggt gtt ttt gag aca gtg gaa atg tta cca tcc aaa gct 6186Leu Tyr Pro Gly Val Phe Glu Thr Val Glu Met Leu Pro Ser Lys Ala 1980 1985 1990gga att tgg cgg gtg gaa tgc ctt att ggc gag cat cta cat gct ggg 6234Gly Ile Trp Arg Val Glu Cys Leu Ile Gly Glu His Leu His Ala Gly 1995 2000 2005atg agc aca ctt ttt ctg gtg tac agc aat aag tgt cag act ccc ctg 6282Met Ser Thr Leu Phe Leu Val Tyr Ser Asn Lys Cys Gln Thr Pro Leu2010 2015 2020 2025gga atg gct tct gga cac att aga gat ttt cag att aca gct tca gga 6330Gly Met Ala Ser Gly His Ile Arg Asp Phe Gln Ile Thr Ala Ser Gly 2030 2035 2040caa tat gga cag tgg gcc cca aag ctg gcc aga ctt cat tat tcc gga 6378Gln Tyr Gly Gln Trp Ala Pro Lys Leu Ala Arg Leu His Tyr Ser Gly 2045 2050 2055tca atc aat gcc tgg agc acc aag gag ccc ttt tct tgg atc aag gtg 6426Ser Ile Asn Ala Trp Ser Thr Lys Glu Pro Phe Ser Trp Ile Lys Val 2060 2065 2070gat ctg ttg gca cca atg att att cac ggc atc aag acc cag ggt gcc 6474Asp Leu Leu Ala Pro Met Ile Ile His Gly Ile Lys Thr Gln Gly Ala 2075 2080 2085cgt cag aag ttc tcc agc ctc tac atc tct cag ttt atc atc atg tat 6522Arg Gln Lys Phe Ser Ser Leu Tyr Ile Ser Gln Phe Ile Ile Met Tyr2090 2095 2100 2105agt ctt gat ggg aag aag tgg cag act tat cga gga aat tcc act gga 6570Ser Leu Asp Gly Lys Lys Trp Gln Thr Tyr Arg Gly Asn Ser Thr Gly 2110 2115 2120acc tta atg gtc ttc ttt ggc aat gtg gat tca tct ggg ata aaa cac 6618Thr Leu Met Val Phe Phe Gly Asn Val Asp Ser Ser Gly Ile Lys His 2125 2130 2135aat att ttt aac cct cca att att gct cga tac atc cgt ttg cac cca 6666Asn Ile Phe Asn Pro Pro Ile Ile Ala Arg Tyr Ile Arg Leu His Pro 2140 2145 2150act cat tat agc att cgc agc act ctt cgc atg gag ttg atg ggc tgt 6714Thr His Tyr Ser Ile Arg Ser Thr Leu Arg Met Glu Leu Met Gly Cys 2155 2160 2165gat tta aat agt tgc agc atg cca ttg gga atg gag agt aaa gca ata 6762Asp Leu Asn Ser Cys Ser Met Pro Leu Gly Met Glu Ser Lys Ala Ile2170 2175 2180 2185tca gat gca cag att act gct tca tcc tac ttt acc aat atg ttt gcc 6810Ser Asp Ala Gln Ile Thr Ala Ser Ser Tyr Phe Thr Asn Met Phe Ala 2190 2195 2200acc tgg tct cct tca aaa gct cga ctt cac ctc caa ggg agg agt aat 6858Thr Trp Ser Pro Ser Lys Ala Arg Leu His Leu Gln Gly Arg Ser Asn 2205 2210 2215gcc tgg aga cct cag gtg aat aat cca aaa gag tgg ctg caa gtg gac 6906Ala Trp Arg Pro Gln Val Asn Asn Pro Lys Glu Trp Leu Gln Val Asp 2220 2225 2230ttc cag aag aca atg aaa gtc aca gga gta act act cag gga gta aaa 6954Phe Gln Lys Thr Met Lys Val Thr Gly Val Thr Thr Gln Gly Val Lys 2235 2240 2245tct ctg ctt acc agc atg tat gtg aag gag ttc ctc atc tcc agc agt 7002Ser Leu Leu Thr Ser Met Tyr Val Lys Glu Phe Leu Ile Ser Ser Ser2250 2255 2260 2265caa gat ggc cat cag tgg act ctc ttt ttt cag aat ggc aaa gta aag 7050Gln Asp Gly His Gln Trp Thr Leu Phe Phe Gln Asn Gly Lys Val Lys 2270 2275 2280gtt ttt cag gga aat caa gac tcc ttc aca cct gtg gtg aac tct cta 7098Val Phe Gln Gly Asn Gln Asp Ser Phe Thr Pro Val Val Asn Ser Leu 2285 2290 2295gac cca ccg tta ctg act cgc tac ctt cga att cac ccc cag agt tgg 7146Asp Pro Pro Leu Leu Thr Arg Tyr Leu Arg Ile His Pro Gln Ser Trp 2300 2305 2310gtg cac cag att gcc ctg agg atg gag gtt ctg ggc tgc gag gca cag 7194Val His Gln Ile Ala Leu Arg Met Glu Val Leu Gly Cys Glu Ala Gln 2315 2320 2325gac ctc tac tgagggtggc cactgcagca cctgccactg ccgtcacctc 7243Asp Leu Tyr2330tccctcctca gctccagggc agtgtccctc cctggcttgc cttctacctt tgtgctaaat 7303cctagcagac actgccttga agcctcctga attaactatc atcagtcctg catttctttg 7363gtggggggcc aggagggtgc atccaattta acttaactct tacctatttt ctgcagctgc 7423tcccagatta ctccttcctt ccaatataac taggcaaaaa gaagtgagga gaaacctgca 7483tgaaagcatt cttccctgaa aagttaggcc tctcagagtc accacttcct ctgttgtaga 7543aaaactatgt gatgaaactt tgaaaaagat atttatgatg ttaacatttc aggttaagcc 7603tcatacgttt aaaataaaac tctcagttgt ttattatcct gatcaagcat ggaacaaagc 7663atgtttcagg atcagatcaa tacaatcttg gagtcaaaag gcaaatcatt tggacaatct 7723gcaaaatgga gagaatacaa taactactac agtaaagtct gtttctgctt ccttacacat 7783agatataatt atgttattta gtcattatga ggggcacatt cttatctcca aaactagcat 7843tcttaaactg agaattatag atggggttca agaatcccta agtcccctga aattatataa 7903ggcattctgt ataaatgcaa atgtgcattt ttctgacgag tgtccataga tataaagcca 7963ttggtcttaa ttctgaccaa taaaaaaata agtcaggagg atgcaattgt tgaaagcttt 8023gaaataaaat aacatgtctt cttgaaattt gtgatggcca agaaagaaaa tgatgatgac 8083attaggcttc taaaggacat acatttaata tttctgtgga aatatgagga aaatccatgg 8143ttatctgaga taggagatac aaactttgta attctaataa tgcactcagt ttactctctc 8203cctctactaa tttcctgctg aaaataacac aacaaaaatg taacagggga aattatatac 8263cgtgactgaa aactagagtc ctacttacat agttgaaata tcaaggaggt cagaagaaaa 8323ttggactggt gaaaacagaa aaaacactcc agtctgccat atcaccacac aataggatcc 8383cccttcttgc cctccacccc cataagattg tgaagggttt actgctcctt ccatctgcct 8443gcaccccttc actatgacta cacagaactc tcctgatagt aaagggggct ggaggcaagg 8503ataagttata gagcagttgg aggaagcatc caaagactgc aacccagggc aaatggaaaa 8563caggagatcc taatatgaaa gaaaaatgga tcccaatctg agaaaaggca aaagaatggc 8623tacttttttc tatgctggag tattttctaa taatcctgct tgacccttat ctgacctctt 8683tggaaactat aacatagctg tcacagtata gtcacaatcc acaaatgatg caggtgcaaa 8743tggtttatag ccctgtgaag ttcttaaagt ttagaggcta acttacagaa atgaataagt 8803tgttttgttt tatagcccgg tagaggagtt aaccccaaag gtgatatggt tttatttcct 8863gttatgttta acttgataat cttattttgg cattcttttc ccattgacta tatacatctc 8923tatttctcaa atgttcatgg aactagctct tttattttcc tgctggtttc ttcagtaatg 8983agttaaataa aacattgaca cataca 9009 2 2332 PRT Homo sapiens 2Ala Thr Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser Trp Asp Tyr 1 5 10 15Met Gln Ser Asp Leu Gly Glu Leu Pro Val Asp Ala Arg Phe Pro Pro 20 25 30Arg Val Pro Lys Ser Phe Pro Phe Asn Thr Ser Val Val Tyr Lys Lys 35 40 45Thr Leu Phe Val Glu Phe Thr Val His Leu Phe Asn Ile Ala Lys Pro 50 55 60Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile Gln Ala Glu Val 65 70 75 80Tyr Asp Thr Val Val Ile Thr Leu Lys Asn Met Ala Ser His Pro Val 85 90 95Ser Leu His Ala Val Gly Val Ser Tyr Trp Lys Ala Ser Glu Gly Ala 100 105 110Glu Tyr Asp Asp Gln Thr Ser Gln Arg Glu Lys Glu Asp Asp Lys Val 115 120 125Phe Pro Gly Gly Ser His Thr Tyr Val Trp Gln Val Leu Lys Glu Asn 130 135 140Gly Pro Met Ala Ser Asp Pro Leu Cys Leu Thr Tyr Ser Tyr Leu Ser145 150 155 160His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu Ile Gly Ala Leu 165 170 175Leu Val Cys Arg Glu Gly Ser Leu Ala Lys Glu Lys Thr Gln Thr Leu 180 185 190His Lys Phe Ile Leu Leu Phe Ala Val Phe Asp Glu Gly Lys Ser Trp 195 200 205His Ser Glu Thr Lys Asn Ser Leu Met Gln Asp Arg Asp Ala Ala Ser 210 215 220Ala Arg Ala Trp Pro Lys Met His Thr Val Asn Gly Tyr Val Asn Arg225 230 235 240Ser Leu Pro Gly Leu Ile Gly Cys His Arg Lys Ser Val Tyr Trp His 245 250 255Val Ile Gly Met Gly Thr Thr Pro Glu Val His Ser Ile Phe Leu Glu 260 265 270Gly His Thr Phe Leu Val Arg Asn His Arg Gln Ala Ser Leu Glu Ile 275 280 285Ser Pro Ile Thr Phe Leu Thr Ala Gln Thr Leu Leu Met Asp Leu Gly 290 295 300Gln Phe Leu Leu Phe Cys His Ile Ser Ser His Gln His Asp Gly Met305 310 315 320Glu Ala Tyr Val Lys Val Asp Ser Cys Pro Glu Glu Pro Gln Leu Arg 325 330 335Met Lys Asn Asn Glu Glu Ala Glu Asp Tyr Asp Asp Asp Leu Thr Asp 340 345 350Ser Glu Met Asp Val Val Arg Phe Asp Asp Asp Asn Ser Pro Ser Phe 355 360 365Ile Gln Ile Arg Ser Val Ala Lys Lys His Pro Lys Thr Trp Val His 370 375 380Tyr Ile Ala Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro Leu Val Leu385 390 395 400Ala Pro Asp Asp Arg Ser Tyr Lys Ser Gln Tyr Leu Asn Asn Gly Pro 405 410 415Gln Arg Ile Gly Arg Lys Tyr Lys Lys Val Arg Phe Met Ala Tyr Thr 420 425 430Asp Glu Thr Phe Lys Thr Arg Glu Ala Ile Gln His Glu Ser Gly Ile 435 440 445Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu Leu Ile Ile 450 455 460Phe Lys Asn Gln Ala Ser Arg Pro Tyr Asn Ile Tyr Pro His Gly Ile465 470 475 480Thr Asp Val Arg Pro Leu Tyr Ser Arg Arg Leu Pro Lys Gly Val Lys 485 490 495His Leu Lys Asp Phe Pro Ile Leu Pro Gly Glu Ile Phe Lys Tyr Lys 500 505 510Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp Pro Arg Cys 515 520 525Leu Thr Arg Tyr Tyr Ser Ser Phe Val Asn Met Glu Arg Asp Leu Ala 530 535 540Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu Ser Val Asp545 550 555 560Gln Arg Gly Asn Gln Ile Met Ser Asp Lys Arg Asn Val Ile Leu Phe 565 570 575Ser Val Phe Asp Glu Asn Arg Ser Trp Tyr Leu Thr Glu Asn Ile Gln 580 585 590Arg Phe Leu Pro Asn Pro Ala Gly Val Gln Leu Glu Asp Pro Glu Phe 595 600 605Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val Phe Asp Ser 610 615 620Leu Gln Leu Ser Val Cys Leu His Glu Val Ala Tyr Trp Tyr Ile Leu625 630 635 640Ser Ile Gly Ala Gln Thr Asp Phe Leu Ser Val Phe Phe Ser Gly Tyr 645 650 655Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr Leu Phe Pro 660 665 670Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro Gly Leu Trp 675 680 685Ile Leu Gly Cys His Asn Ser Asp Phe Arg Asn Arg Gly Met Thr Ala 690 695 700Leu Leu Lys Val Ser Ser Cys Asp Lys Asn Thr Gly Asp Tyr Tyr Glu705 710 715 720Asp Ser Tyr Glu Asp Ile Ser Ala Tyr Leu Leu Ser Lys Asn Asn Ala 725 730 735Ile Glu Pro Arg Ser Phe Ser Gln Asn Ser Arg His Pro Ser Thr Arg 740 745 750Gln Lys Gln Phe Asn Ala Thr Thr Ile Pro Glu Asn Asp Ile Glu Lys 755 760 765Thr Asp Pro Trp Phe Ala His Arg Thr Pro Met Pro Lys Ile Gln Asn 770 775 780Val Ser Ser Ser Asp Leu Leu Met Leu Leu Arg Gln Ser Pro Thr Pro785 790 795 800His Gly Leu Ser Leu Ser Asp Leu Gln Glu Ala Lys Tyr Glu Thr Phe 805 810 815Ser Asp Asp Pro Ser Pro Gly Ala Ile Asp Ser Asn Asn Ser Leu Ser 820 825 830Glu Met Thr His Phe Arg Pro Gln Leu His His Ser Gly Asp Met Val 835 840 845Phe Thr Pro Glu Ser Gly Leu Gln Leu Arg Leu Asn Glu Lys Leu Gly 850 855 860Thr Thr Ala Ala Thr Glu Leu Lys Lys Leu Asp Phe Lys Val Ser Ser865 870 875 880Thr Ser Asn Asn Leu Ile Ser Thr Ile Pro Ser Asp Asn Leu Ala Ala 885 890 895Gly Thr Asp Asn Thr Ser Ser Leu Gly Pro Pro Ser Met Pro Val His 900 905 910Tyr Asp Ser Gln Leu Asp Thr Thr Leu Phe Gly Lys Lys Ser Ser Pro 915 920 925Leu Thr Glu Ser Gly Gly Pro Leu Ser Leu Ser Glu Glu Asn Asn Asp 930 935 940Ser Lys Leu Leu Glu Ser Gly Leu Met Asn Ser Gln Glu Ser Ser Trp945 950 955 960Gly Lys Asn Val Ser Ser Thr Glu Ser Gly Arg Leu Phe Lys Gly Lys 965 970 975Arg Ala His Gly Pro Ala Leu Leu Thr Lys Asp Asn Ala Leu Phe Lys 980 985 990Val Ser Ile Ser Leu Leu Lys Thr Asn Lys Thr Ser Asn Asn Ser Ala 995 1000 1005Thr Asn Arg Lys Thr His Ile Asp Gly Pro Ser Leu Leu Ile Glu Asn 1010 1015 1020Ser Pro Ser Val Trp Gln Asn Ile Leu Glu Ser Asp Thr Glu Phe Lys025 1030 1035 1040Lys Val Thr Pro Leu Ile His Asp Arg Met Leu Met Asp Lys Asn Ala 1045 1050 1055Thr Ala Leu Arg Leu Asn His Met Ser Asn Lys Thr Thr Ser Ser Lys 1060 1065 1070Asn Met Glu Met Val Gln Gln Lys Lys Glu Gly Pro Ile Pro Pro Asp 1075 1080 1085Ala Gln Asn Pro Asp Met Ser Phe Phe Lys Met Leu Phe Leu Pro Glu 1090 1095 1100Ser Ala Arg Trp Ile Gln Arg Thr His Gly Lys Asn Ser Leu Asn Ser105 1110 1115 1120Gly Gln Gly Pro Ser Pro Lys Gln Leu Val Ser Leu Gly Pro Glu Lys 1125 1130 1135Ser Val Glu Gly Gln Asn Phe Leu Ser Glu Lys Asn Lys Val Val Val 1140 1145 1150Gly Lys Gly Glu Phe Thr Lys Asp Val Gly Leu Lys Glu Met Val Phe 1155 1160 1165Pro Ser Ser Arg Asn Leu Phe Leu Thr Asn Leu Asp Asn Leu His Glu 1170 1175 1180Asn Asn Thr His Asn Gln Glu Lys Lys Ile Gln Glu Glu Ile Glu Lys185 1190 1195 1200Lys Glu Thr Leu Ile Gln Glu Asn Val Val Leu Pro Gln Ile His Thr 1205 1210 1215Val Thr Gly Thr Lys Asn Phe Met Lys Asn Leu Phe Leu Leu Ser Thr 1220 1225 1230Arg Gln Asn Val Glu Gly Ser Tyr Glu Gly Ala Tyr Ala Pro Val Leu 1235 1240 1245Gln Asp Phe Arg Ser Leu Asn Asp Ser Thr Asn Arg Thr Lys Lys His 1250 1255 1260Thr Ala His Phe Ser Lys Lys Gly Glu Glu Glu Asn Leu Glu Gly Leu265 1270 1275 1280Gly Asn Gln Thr Lys Gln Ile Val Glu Lys Tyr Ala Cys Thr Thr Arg 1285 1290 1295Ile Ser Pro Asn Thr Ser Gln Gln Asn Phe Val Thr Gln Arg Ser Lys 1300 1305 1310Arg Ala Leu Lys Gln Phe Arg Leu Pro Leu Glu Glu Thr Glu Leu Glu 1315 1320 1325Lys Arg Ile Ile Val Asp Asp Thr Ser Thr Gln Trp Ser Lys Asn Met 1330 1335 1340Lys His Leu Thr Pro Ser Thr Leu Thr Gln Ile Asp Tyr Asn Glu Lys345 1350 1355 1360Glu Lys Gly Ala Ile Thr Gln Ser Pro Leu Ser Asp Cys Leu Thr Arg 1365 1370 1375Ser His Ser Ile Pro Gln Ala Asn Arg Ser Pro Leu Pro Ile Ala Lys 1380 1385 1390Val Ser Ser Phe Pro Ser Ile Arg Pro Ile Tyr Leu Thr Arg Val Leu 1395 1400 1405Phe Gln Asp Asn Ser Ser His Leu Pro Ala Ala Ser Tyr Arg Lys Lys 1410 1415 1420Asp Ser Gly Val Gln Glu Ser Ser His Phe Leu Gln Gly Ala Lys Lys425 1430 1435 1440Asn Asn Leu Ser Leu Ala Ile Leu Thr Leu Glu Met Thr Gly Asp Gln 1445 1450 1455Arg Glu Val Gly Ser Leu Gly Thr Ser Ala Thr Asn Ser Val Thr Tyr 1460 1465 1470Lys Lys Val Glu Asn Thr Val Leu Pro Lys Pro Asp Leu Pro Lys Thr 1475 1480 1485Ser Gly Lys Val Glu Leu Leu Pro Lys Val His Ile Tyr Gln Lys Asp 1490 1495 1500Leu Phe Pro Thr Glu Thr Ser Asn Gly Ser Pro Gly His Leu Asp Leu505 1510 1515 1520Val Glu Gly Ser Leu Leu Gln Gly Thr Glu Gly Ala Ile Lys Trp Asn 1525 1530 1535Glu Ala Asn Arg Pro Gly Lys Val Pro Phe Leu Arg Val Ala Thr Glu 1540 1545 1550Ser Ser Ala Lys Thr Pro Ser Lys Leu Leu Asp Pro Leu Ala Trp Asp 1555 1560 1565Asn His Tyr Gly Thr Gln Ile Pro Lys Glu Glu Trp Lys Ser Gln Glu 1570 1575 1580Lys Ser Pro Glu Lys Thr Ala Phe Lys Lys Lys Asp Thr Ile Leu Ser585 1590 1595 1600Leu Asn Ala Cys Glu Ser Asn His Ala Ile Ala Ala Ile Asn Glu Gly 1605 1610 1615Gln Asn Lys Pro Glu Ile Glu Val Thr Trp Ala Lys Gln Gly Arg Thr 1620 1625 1630Glu Arg Leu Cys Ser Gln Asn Pro Pro Val Leu Lys Arg His Gln Arg 1635 1640 1645Glu Ile Thr Arg Thr Thr Leu Gln Ser Asp Gln Glu Glu Ile Asp Tyr 1650 1655 1660Asp Asp Thr Ile Ser Val Glu Met Lys Lys Glu Asp Phe Asp Ile Tyr665 1670 1675 1680Asp Glu Asp Glu Asn Gln Ser Pro Arg Ser Phe Gln Lys Lys Thr Arg 1685 1690 1695His Tyr Phe Ile Ala Ala Val Glu Arg Leu Trp Asp Tyr Gly Met Ser 1700 1705 1710Ser Ser Pro His Val Leu Arg Asn Arg Ala Gln Ser Gly Ser Val Pro 1715 1720 1725Gln Phe Lys Lys Val Val Phe Gln Glu Phe Thr Asp Gly Ser Phe Thr 1730 1735 1740Gln Pro Leu Tyr Arg Gly Glu Leu Asn Glu His Leu Gly Leu Leu Gly745 1750 1755 1760Pro Tyr Ile Arg Ala Glu Val Glu Asp Asn Ile Met Val Thr Phe Arg 1765 1770 1775Asn Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser Ser Leu Ile Ser Tyr 1780 1785 1790Glu Glu Asp Gln Arg Gln Gly Ala Glu Pro Arg Lys Asn Phe Val Lys 1795 1800 1805Pro Asn Glu Thr Lys Thr Tyr Phe Trp Lys Val Gln His His Met Ala 1810 1815 1820Pro Thr Lys Asp Glu Phe Asp Cys Lys Ala Trp Ala Tyr Phe Ser Asp825 1830 1835 1840Val Asp Leu Glu Lys Asp Val His Ser Gly Leu Ile Gly Pro Leu Leu 1845 1850 1855Val Cys His Thr Asn Thr Leu Asn Pro Ala His Gly Arg Gln Val Thr 1860 1865 1870Val Gln Glu Phe Ala Leu Phe Phe Thr Ile Phe Asp Glu Thr Lys Ser 1875 1880 1885Trp Tyr Phe Thr Glu Asn Met Glu Arg Asn Cys Arg Ala Pro Cys Asn 1890 1895 1900Ile Gln Met Glu Asp Pro Thr Phe Lys Glu Asn Tyr Arg Phe His Ala905 1910 1915 1920Ile Asn Gly Tyr Ile Met Asp Thr Leu Pro Gly Leu Val Met Ala Gln 1925 1930 1935Asp Gln Arg Ile Arg Trp Tyr Leu Leu Ser Met Gly Ser Asn Glu Asn 1940 1945 1950Ile His Ser Ile His Phe Ser Gly His Val Phe Thr Val Arg Lys Lys 1955 1960 1965Glu Glu Tyr Lys Met Ala Leu Tyr Asn Leu Tyr Pro Gly Val Phe Glu 1970 1975 1980Thr Val Glu Met Leu Pro Ser Lys Ala Gly Ile Trp Arg Val Glu Cys985 1990 1995 2000Leu Ile Gly Glu His Leu His Ala Gly Met Ser Thr Leu Phe Leu Val 2005 2010 2015Tyr Ser Asn Lys Cys Gln Thr Pro Leu Gly Met Ala Ser Gly His Ile 2020 2025 2030Arg Asp Phe Gln Ile Thr Ala Ser Gly Gln Tyr Gly Gln Trp Ala Pro 2035 2040 2045Lys Leu Ala Arg Leu His Tyr Ser Gly Ser Ile Asn Ala Trp Ser Thr 2050 2055 2060Lys Glu Pro Phe Ser Trp Ile Lys Val Asp Leu Leu Ala Pro Met Ile065 2070 2075 2080Ile His Gly Ile Lys Thr Gln Gly Ala Arg Gln Lys Phe Ser Ser Leu 2085 2090 2095Tyr Ile Ser Gln Phe Ile Ile Met Tyr Ser Leu Asp Gly Lys Lys Trp 2100 2105 2110Gln Thr Tyr Arg Gly Asn Ser Thr Gly Thr Leu Met Val Phe Phe Gly 2115 2120 2125Asn Val Asp Ser Ser Gly Ile Lys His Asn Ile Phe Asn Pro Pro Ile 2130 2135 2140Ile Ala Arg Tyr Ile Arg Leu His Pro Thr His Tyr Ser Ile Arg Ser145 2150 2155 2160Thr Leu Arg Met Glu Leu Met Gly Cys Asp Leu Asn Ser Cys Ser Met 2165 2170 2175Pro Leu Gly Met Glu Ser Lys Ala Ile Ser Asp Ala Gln Ile Thr Ala 2180 2185 2190Ser Ser Tyr Phe Thr Asn Met Phe Ala Thr Trp Ser Pro Ser Lys Ala 2195 2200 2205Arg Leu His Leu Gln Gly Arg Ser Asn Ala Trp Arg Pro Gln Val Asn 2210 2215 2220Asn Pro Lys Glu Trp Leu Gln Val Asp Phe Gln Lys Thr Met Lys Val225 2230 2235 2240Thr Gly Val Thr Thr Gln Gly Val Lys Ser Leu Leu Thr Ser Met Tyr 2245 2250 2255Val Lys Glu Phe Leu Ile Ser Ser Ser Gln Asp Gly His Gln Trp Thr 2260 2265 2270Leu Phe Phe Gln Asn Gly Lys Val Lys Val Phe Gln Gly Asn Gln Asp 2275 2280 2285Ser Phe Thr Pro Val Val Asn Ser Leu Asp Pro Pro Leu Leu Thr Arg 2290 2295 2300Tyr Leu Arg Ile His Pro Gln Ser Trp Val His Gln Ile Ala Leu Arg305 2310 2315 2320Met Glu Val Leu Gly Cys Glu Ala Gln Asp Leu Tyr 2325 2330 3 1130 DNA Porcine 3taagcaccct aagacgtggg tgcactacat ctctgcagag gaggaggact gggactacgc 60ccccgcggtc cccagcccca gtgacagaag ttataaaagt ctctacttga acagtggtcc 120tcagcgaatt ggtaggaaat acaaaaaagc tcgattcgtc gcttacacgg atgtaacatt 180taagactcgt aaagctattc cgtatgaatc aggaatcctg ggacctttac tttatggaga 240agttggagac acacttttga ttatatttaa gaataaagcg agccgaccat ataacatcta 300ccctcatgga atcactgatg tcagcgcttt gcacccaggg agacttctaa aaggttggaa 360acatttgaaa gacatgccaa ttctgccagg agagactttc aagtataaat ggacagtgac 420tgtggaagat gggccaacca agtccgatcc tcggtgcctg acccgctact actcgagctc 480cattaatcta gagaaagatc tggcttcggg actcattggc cctctcctca tctgctacaa 540agaatctgta gaccaaagag gaaaccagat gatgtcagac aagagaaacg tcatcctgtt 600ttctgtattc gatgagaatc aaagctggta cctcgcagag aatattcagc gcttcctccc 660caatccggat ggattacagc cccaggatcc agagttccaa gcttctaaca tcatgcacag 720catcaatggc tatgtttttg atagcttgca gctgtcggtt tgtttgcacg aggtggcata 780ctggtacatt ctaagtgttg gagcacagac ggacttcctc tccgtcttct tctctggcta 840caccttcaaa cacaaaatgg tctatgaaga cacactcacc ctgttcccct tctcaggaga 900aacggtcttc atgtcaatgg aaaacccagg tctctgggtc ctagggtgcc acaactcaga 960cttgcggaac agagggatga cagccttact gaaggtgtat agttgtgaca gggacattgg 1020tgattattat gacaacactt atgaagatat tccaggcttc ttgctgagtg gaaagaatgt 1080cattgaaccc agaagctttg cccagaattc aagaccccct agtgcgagca 1130 4 368 PRT Porcine 4Ser Val Ala Lys Lys His Pro Lys Thr Trp Val His Tyr Ile Ser Ala 1 5 10 15Glu Glu Glu Asp Trp Asp Tyr Ala Pro Ala Val Pro Ser Pro Ser Asp 20 25 30Arg Ser Tyr Lys Ser Leu Tyr Leu Asn Ser Gly Pro Gln Arg Ile Gly 35 40 45Arg Lys Tyr Lys Lys Ala Arg Phe Val Ala Tyr Thr Asp Val Thr Phe 50 55 60Lys Thr Arg Lys Ala Ile Pro Tyr Glu Ser Gly Ile Leu Gly Pro Leu 65 70 75 80Leu Tyr Gly Glu Val Gly Asp Thr Leu Leu Ile Ile Phe Lys Asn Lys 85 90 95Ala Ser Arg Pro Tyr Asn Ile Tyr Pro His Gly Ile Thr Asp Val Ser 100 105 110Ala Leu His Pro Gly Arg Leu Leu Lys Gly Trp Lys His Leu Lys Asp 115 120 125Met Pro Ile Leu Pro Gly Glu Thr Phe Lys Tyr Lys Trp Thr Val Thr 130 135 140Val Glu Asp Gly Pro Thr Lys Ser Asp Pro Arg Cys Leu Thr Arg Tyr145 150 155 160Tyr Ser Ser Ser Ile Asn Leu Glu Lys Asp Leu Ala Ser Gly Leu Ile 165 170 175Gly Pro Leu Leu Ile Cys Tyr Lys Glu Ser Val Asp Gln Arg Gly Asn 180 185 190Gln Met Met Ser Asp Lys Arg Asn Val Ile Leu Phe Ser Val Phe Asp 195 200 205Glu Asn Gln Ser Trp Tyr Leu Ala Glu Asn Ile Gln Arg Phe Leu Pro 210 215 220Asn Pro Asp Gly Leu Gln Pro Gln Asp Pro Glu Phe Gln Ala Ser Asn225 230 235 240Ile Met His Ser Ile Asn Gly Tyr Val Phe Asp Ser Leu Gln Leu Ser 245 250 255Val Cys Leu His Glu Val Ala Tyr Trp Tyr Ile Leu Ser Val Gly Ala 260 265 270Gln Thr Asp Phe Leu Ser Val Phe Phe Ser Gly Tyr Thr Phe Lys His 275 280 285Lys Met Val Tyr Glu Asp Thr Leu Thr Leu Phe Pro Phe Ser Gly Glu 290 295 300Thr Val Phe Met Ser Met Glu Asn Pro Gly Leu Trp Val Leu Gly Cys305 310 315 320His Asn Ser Asp Leu Arg Asn Arg Gly Met Thr Ala Leu Leu Lys Val 325 330 335Tyr Ser Cys Asp Arg Asp Ile Gly Asp Tyr Tyr Asp Asn Thr Tyr Glu 340 345 350Asp Ile Pro Gly Phe Leu Leu Ser Gly Lys Asn Val Ile Glu Pro Arg 355 360 365 5 44 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 5ctaatacgac tcactatagg gctcgagcgg ccgcccgggc aggt 44 6 27 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 6catcctaat acgactcact atagggc 27 7 24 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 7ccattgacat gaagaccgtt tctc 24 8 23 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 8actcactata gggctcgagc ggc 23 9 24 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 9gggtgcaaag cgctgacatc agtg 24 10 50 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 10cctctcgagc caccatgtcg agccaccatg cagctagagc tctccacctg 50 11 31 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 11cgcgcggccg cgcatctggc aaagctgagt t 31 12 27 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 12gaaataagcc caggctttgc agtcraa 27 13 22 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 13aggaaattcc actggaacct tn 22 14 25 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 14ctgggggtga attcgaaggt agcgn 25 15 23 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 15gagttcatcg ggaagacctg ttg 23 16 24 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 16acagcccatc aactccatgc gaag 24 17 19 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 17tcagggcaat caggactcc 19 18 21 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 18ccgtggtgaa cgctctggac c 21 19 24 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 19gtagaggtcc tgtgcctcgc agcc 24 20 27 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 20gtagagstsc tgkgcctcrc akccyag 27 21 24 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 21cttcgcatgg agttgatggg ctgt 24 22 22 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 22aatcaggact cctccacccc cg 22 23 20 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 23ggatccaccc cacgagctgg 20 24 24 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 24cgccctgagg ctcgaggttc tagg 24 25 22 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 25aatcaggact cctccacccc cg 22 26 20 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 26ccttgcagga attcgattca 20 27 21 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 27ccgtggtgaa cgctctggac c 21 28 2319 PRT Mus musculus 28Met Gln Ile Ala Leu Phe Ala Cys Phe Phe Leu Ser Leu Phe Asn Phe 1 5 10 15Cys Ser Ser Ala Ile Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser 20 25 30Trp Asn Tyr Ile Gln Ser Asp Leu Leu Ser Val Leu His Thr Asp Ser 35 40 45Arg Phe Leu Pro Arg Met Ser Thr Ser Phe Pro Phe Asn Thr Ser Ile 50 55 60Met Tyr Lys Lys Thr Val Phe Val Glu Tyr Lys Asp Gln Leu Phe Asn 65 70 75 80Ile Ala Lys Pro Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile 85 90 95Trp Thr Glu Val His Asp Thr Val Val Ile Thr Leu Lys Asn Met Ala 100 105 110Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Tyr Trp Lys Ala 115 120 125Ser Glu Gly Asp Glu Tyr Glu Asp Gln Thr Ser Gln Met Glu Lys Glu 130 135 140Asp Asp Lys Val Phe Pro Gly Glu Ser His Thr Tyr Val Trp Gln Val145 150 155 160Leu Lys Glu Asn Gly Pro Met Ala Ser Asp Pro Pro Cys Leu Thr Tyr 165 170 175Ser Tyr Met Ser His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu 180 185 190Ile Gly Ala Leu Leu Val Cys Lys Glu Gly Ser Leu Ser Lys Glu Arg 195 200 205Thr Gln Met Leu Tyr Gln Phe Val Leu Leu Phe Ala Val Phe Asp Glu 210 215 220Gly Lys Ser Trp His Ser Glu Thr Asn Asp Ser Tyr Thr Gln Ser Met225 230 235 240Asp Ser Ala Ser Ala Arg Asp Trp Pro Lys Met His Thr Val Asn Gly 245 250 255Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His Arg Lys Ser 260 265 270Val Tyr Trp His Val Ile Gly Met Gly Thr Thr Pro Glu Ile His Ser 275 280 285Ile Phe Leu Glu Gly His Thr Phe Phe Val Arg Asn His Arg Gln Ala 290 295 300Ser Leu Glu Ile Ser Pro Ile Thr Phe Leu Thr Ala Gln Thr Leu Leu305 310 315 320Ile Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser Ser His Lys 325 330 335His Asp Gly Met Glu Ala Tyr Val Lys Val Asp Ser Cys Pro Glu Glu 340 345 350Ser Gln Trp Gln Lys Lys Asn Asn Asn Glu Glu Met Glu Asp Tyr Asp 355 360 365Asp Asp Leu Tyr Ser Glu Met Asp Met Phe Thr Leu Asp Tyr Asp Ser 370 375 380Ser Pro Phe Ile Gln Ile Arg Ser Val Ala Lys Lys Tyr Pro Lys Thr385 390 395 400Trp Ile His Tyr Ile Ser Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro 405 410 415Ser Val Pro Thr Ser Asp Asn Gly Ser Tyr Lys Ser Gln Tyr Leu Ser 420 425 430Asn Gly Pro His Arg Ile Gly Arg Lys Tyr Lys Lys Val Arg Phe Ile 435 440 445Ala Tyr Thr Asp Glu Thr Phe Lys Thr Arg Glu Thr Ile Gln His Glu 450 455 460Ser Gly Leu Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu465 470 475 480Leu Ile Ile Phe Lys Asn Gln Ala Ser Arg Pro Tyr Asn Ile Tyr Pro 485 490 495His Gly Ile Thr Asp Val Ser Pro Leu His Ala Arg Arg Leu Pro Arg 500 505 510Gly Ile Lys His Val Lys Asp Leu Pro Ile His Pro Gly Glu Ile Phe 515 520 525Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp 530 535 540Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Phe Ile Asn Pro Glu Arg545 550 555 560Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu 565 570 575Ser Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn Val 580 585 590Ile Leu Phe Ser Ile Phe Asp Glu Asn Gln Ser Trp Tyr Ile Thr Glu 595 600 605Asn Met Gln Arg Phe Leu Pro Asn Ala Ala Lys Thr Gln Pro Gln Asp 610 615 620Pro Gly Phe Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val625 630 635 640Phe Asp Ser Leu Glu Leu Thr Val Cys Leu His Glu Val Ala Tyr Trp 645 650 655His Ile Leu Ser Val Gly Ala Gln Thr Asp Phe Leu Ser Ile Phe Phe 660 665 670Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr 675 680 685Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro 690 695 700Gly Leu Trp Val Leu Gly Cys His Asn Ser Asp Phe Arg Lys Arg Gly705 710 715 720Met Thr Ala Leu Leu Lys Val Ser Ser Cys Asp Lys Ser Thr Ser Asp 725 730 735Tyr Tyr Glu Glu Ile Tyr Glu Asp Ile Pro Thr Gln Leu Val Asn Glu 740 745 750Asn Asn Val Ile Asp Pro Arg Ser Phe Phe Gln Asn Thr Asn His Pro 755 760 765Asn Thr Arg Lys Lys Lys Phe Lys Asp Ser Thr Ile Pro Lys Asn Asp 770 775 780Met Glu Lys Ile Glu Pro Gln Phe Glu Glu Ile Ala Glu Met Leu Lys785 790 795 800Val Gln Ser Val Ser Val Ser Asp Met Leu Met Leu Leu Gly Gln Ser 805 810 815His Pro Thr Pro His Gly Leu Phe Leu Ser Asp Gly Gln Glu Ala Ile 820 825 830Tyr Glu Ala Ile His Asp Asp His Ser Pro Asn Ala Ile Asp Ser Asn 835 840 845Glu Gly Pro Ser Lys Val Thr Gln Leu Arg Pro Glu Ser His His Ser 850 855 860Glu Lys Ile Val Phe Thr Pro Gln Pro Gly Leu Gln Leu Arg Ser Asn865 870 875 880Lys Ser Leu Glu Thr Thr Ile Glu Val Lys Trp Lys Lys Leu Gly Leu 885 890 895Gln Val Ser Ser Leu Pro Ser Asn Leu Met Thr Thr Thr Ile Leu Ser 900 905 910Asp Asn Leu Lys Ala Thr Phe Glu Lys Thr Asp Ser Ser Gly Phe Pro 915 920 925Asp Met Pro Val His Ser Ser Ser Lys Leu Ser Thr Thr Ala Phe Gly 930 935 940Lys Lys Ala Tyr Ser Leu Val Gly Ser His Val Pro Leu Asn Ala Ser945 950 955 960Glu Glu Asn Ser Asp Ser Asn Ile Leu Asp Ser Thr Leu Met Tyr Ser 965 970 975Gln Glu Ser Leu Pro Arg Asp Asn Ile Leu Ser Ile Glu Asn Asp Arg 980 985 990Leu Leu Arg Glu Lys Arg Phe His Gly Ile Ala Leu Leu Thr Lys Asp 995 1000 1005Asn Thr Leu Phe Lys Asp Asn Val Ser Leu Met Lys Thr Asn Lys Thr 1010 1015 1020Tyr Asn His Ser Thr Thr Asn Glu Lys Leu His Thr Glu Ser Pro Thr1025 1030 1035 1040Ser Ile Glu Asn Ser Thr Thr Asp Leu Gln Asp Ala Ile Leu Lys Val 1045 1050 1055Asn Ser Glu Ile Gln Glu Val Thr Ala Leu Ile His Asp Gly Thr Leu 1060 1065 1070Leu Gly Lys Asn Ser Thr Tyr Leu Arg Leu Asn His Met Leu Asn Arg 1075 1080 1085Thr Thr Ser Thr Lys Asn Lys Asp Ile Phe His Arg Lys Asp Glu Asp 1090 1095 1100Pro Ile Pro Gln Asp Glu Glu Asn Thr Ile Met Pro Phe Ser Lys Met1105 1110 1115 1120Leu Phe Leu Ser Glu Ser Ser Asn Trp Phe Lys Lys Thr Asn Gly Asn 1125 1130 1135Asn Ser Leu Asn Ser Glu Gln Glu His Ser Pro Lys Gln Leu Val Tyr 1140 1145 1150Leu Met Phe Lys Lys Tyr Val Lys Asn Gln Ser Phe Leu Ser Glu Lys 1155 1160 1165Asn Lys Val Thr Val Glu Gln Asp Gly Phe Thr Lys Asn Ile Gly Leu 1170 1175 1180Lys Asp Met Ala Phe Pro His Asn Met Ser Ile Phe Leu Thr Thr Leu1185 1190 1195 1200Ser Asn Val His Glu Asn Gly Arg His Asn Gln Glu Lys Asn Ile Gln 1205 1210 1215Glu Glu Ile Glu Lys Glu Ala Leu Ile Glu Glu Lys Val Val Leu Pro 1220 1225 1230Gln Val His Glu Ala Thr Gly Ser Lys Asn Phe Leu Lys Asp Ile Leu 1235 1240 1245Ile Leu Gly Thr Arg Gln Asn Ile Ser Leu Tyr Glu Val His Val Pro 1250 1255 1260Val Leu Gln Asn Ile Thr Ser Ile Asn Asn Ser Thr Asn Thr Val Gln1265 1270 1275 1280Ile His Met Glu His Phe Phe Lys Arg Arg Lys Asp Lys Glu Thr Asn 1285 1290 1295Ser Glu Gly Leu Val Asn Lys Thr Arg Glu Met Val Lys Asn Tyr Pro 1300 1305 1310Ser Gln Lys Asn Ile Thr Thr Gln Arg Ser Lys Arg Ala Leu Gly Gln 1315 1320 1325Phe Arg Leu Ser Thr Gln Trp Leu Lys Thr Ile Asn Cys Ser Thr Gln 1330 1335 1340Cys Ile Ile Lys Gln Ile Asp His Ser Lys Glu Met Lys Lys Phe Ile1345 1350 1355 1360Thr Lys Ser Ser Leu Ser Asp Ser Ser Val Ile Lys Ser Thr Thr Gln 1365 1370 1375Thr Asn Ser Ser Asp Ser His Ile Val Lys Thr Ser Ala Phe Pro Pro 1380 1385 1390Ile Asp Leu Lys Arg Ser Pro Phe Gln Asn Lys Phe Ser His Val Gln 1395 1400 1405Ala Ser Ser Tyr Ile Tyr Asp Phe Lys Thr Lys Ser Ser Arg Ile Gln 1410 1415 1420Glu Ser Asn Asn Phe Leu Lys Glu Thr Lys Ile Asn Asn Pro Ser Leu1425 1430 1435 1440Ala Ile Leu Pro Trp Asn Met Phe Ile Asp Gln Gly Lys Phe Thr Ser 1445 1450 1455Pro Gly Lys Ser Asn Thr Asn Ser Val Thr Tyr Lys Lys Arg Glu Asn 1460 1465 1470Ile Ile Phe Leu Lys Pro Thr Leu Pro Glu Glu Ser Gly Lys Ile Glu 1475 1480 1485Leu Leu Pro Gln Val Ser Ile Gln Glu Glu Glu Ile Leu Pro Thr Glu 1490 1495 1500Thr Ser His Gly Ser Pro Gly His Leu Asn Leu Met Lys Glu Val Phe1505 1510 1515 1520Leu Gln Lys Ile Gln Gly Pro Thr Lys Trp Asn Lys Ala Lys Arg His 1525 1530 1535Gly Glu Ser Ile Lys Gly Lys Thr Glu Ser Ser Lys Asn Thr Arg Ser 1540 1545 1550Lys Leu Leu Asn His His Ala Trp Asp Tyr His Tyr Ala Ala Gln Ile 1555 1560 1565Pro Lys Asp Met Trp Lys Ser Lys Glu Lys Ser Pro Glu Ile Ile Ser 1570 1575 1580Ile Lys Gln Glu Asp Thr Ile Leu Ser Leu Arg Pro His Gly Asn Ser1585 1590 1595 1600His Ser Ile Gly Ala Asn Glu Lys Gln Asn Trp Pro Gln Arg Glu Thr 1605 1610 1615Thr Trp Val Lys Gln Gly Gln Thr Gln Arg Thr Cys Ser Gln Ile Pro 1620 1625 1630Pro Val Leu Lys Arg His Gln Arg Glu Leu Ser Ala Phe Gln Ser Glu 1635 1640 1645Gln Glu Ala Thr Asp Tyr Asp Asp Ala Ile Thr Ile Glu Thr Ile Glu 1650 1655 1660Asp Phe Asp Ile Tyr Ser Glu Asp Ile Lys Gln Gly Pro Arg Ser Phe1665 1670 1675 1680Gln Gln Lys Thr Arg His Tyr Phe Ile Ala Ala Val Glu Arg Leu Trp 1685 1690 1695Asp Tyr Gly Met Ser Thr Ser His Val Leu Arg Asn Arg Tyr Gln Ser 1700 1705 1710Asp Asn Val Pro Gln Phe Lys Lys Val Val Phe Gln Glu Phe Thr Asp 1715 1720 1725Gly Ser Phe Ser Gln Pro Leu Tyr Arg Gly Glu Leu Asn Glu His Leu 1730 1735 1740Gly Leu Leu Gly Pro Tyr Ile Arg Ala Glu Val Glu Asp Asn Ile Met1745 1750 1755 1760Val Thr Phe Lys Asn Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser Ser 1765 1770 1775Leu Ile Ser Tyr Lys Glu Asp Gln Arg Gly Glu Glu Pro Arg Arg Asn 1780 1785 1790Phe Val Lys Pro Asn Glu Thr Lys Ile Tyr Phe Trp Lys Val Gln His 1795 1800 1805His Met Ala Pro Thr Glu Asp Glu Phe Asp Cys Lys Ala Trp Ala Tyr 1810 1815 1820Phe Ser Asp Val Asp Leu Glu Arg Asp Met His Ser Gly Leu Ile Gly1825 1830 1835 1840Pro Leu Leu Ile Cys His Ala Asn Thr Leu Asn Pro Ala His Gly Arg 1845 1850 1855Gln Val Ser Val Gln Glu Phe Ala Leu Leu Phe Thr Ile Phe Asp Glu 1860 1865 1870Thr Lys Ser Trp Tyr Phe Thr Glu Asn Val Lys Arg Asn Cys Lys Thr 1875 1880 1885Pro Cys Asn Phe Gln Met Glu Asp Pro Thr Leu Lys Glu Asn Tyr Arg 1890 1895 1900Phe His Ala Ile Asn Gly Tyr Val Met Asp Thr Leu Pro Gly Leu Val1905 1910 1915 1920Met Ala Gln Asp Gln Arg Ile Arg Trp Tyr Leu Leu Ser Met Gly Asn 1925 1930 1935Asn Glu Asn Ile Gln Ser Ile His Phe Ser Gly His Val Phe Thr Val 1940 1945 1950Arg Lys Lys Glu Glu Tyr Lys Met Ala Val Tyr Asn Leu Tyr Pro Gly 1955 1960 1965Val Phe Glu Thr Leu Glu Met Ile Pro Ser Arg Ala Gly Ile Trp Arg 1970 1975 1980Val Glu Cys Leu Ile Gly Glu His Leu Gln Ala Gly Met Ser Thr Leu1985 1990 1995 2000Phe Leu Val Tyr Ser Lys Gln Cys Gln Ile Pro Leu Gly Met Ala Ser 2005 2010 2015Gly Ser Ile Arg Asp Phe Gln Ile Thr Ala Ser Gly His Tyr Gly Gln 2020 2025 2030Trp Ala Pro Asn Leu Ala Arg Leu His Tyr Ser Gly Ser Ile Asn Ala 2035 2040 2045Trp Ser Thr Lys Glu Pro Phe Ser Trp Ile Lys Val Asp Leu Leu Ala 2050 2055 2060Pro Met Ile Val His Gly Ile Lys Thr Gln Gly Ala Arg Gln Lys Phe2065 2070 2075 2080Ser Ser Leu Tyr Ile Ser Gln Phe Ile Ile Met Tyr Ser Leu Asp Gly 2085 2090 2095Lys Lys Trp Leu Ser Tyr Gln Gly Asn Ser Thr Gly Thr Leu Met Val 2100 2105 2110Phe Phe Gly Asn Val Asp Ser Ser Gly Ile Lys His Asn Ser Phe Asn 2115 2120 2125Pro Pro Ile Ile Ala Arg Tyr Ile Arg Leu His Pro Thr His Ser Ser 2130 2135 2140Ile Arg Ser Thr Leu Arg Met Glu Leu Met Gly Cys Asp Leu Asn Ser2145 2150 2155 2160Cys Ser Ile Pro Leu Gly Met Glu Ser Lys Val Ile Ser Asp Thr Gln 2165 2170 2175Ile Thr Ala Ser Ser Tyr Phe Thr Asn Met Phe Ala Thr Trp Ser Pro 2180 2185 2190Ser Gln Ala Arg Leu His Leu Gln Gly Arg Thr Asn Ala Trp Arg Pro 2195 2200 2205Gln Val Asn Asp Pro Lys Gln Trp Leu Gln Val Asp Leu Gln Lys Thr 2210 2215 2220Met Lys Val Thr Gly Ile Ile Thr Gln Gly Val Lys Ser Leu Phe Thr2225 2230 2235 2240Ser Met Phe Val Lys Glu Phe Leu Ile Ser Ser Ser Gln Asp Gly His 2245 2250 2255His Trp Thr Gln Ile Leu Tyr Asn Gly Lys Val Lys Val Phe Gln Gly 2260 2265 2270Asn Gln Asp Ser Ser Thr Pro Met Met Asn Ser Leu Asp Pro Pro Leu 2275 2280 2285Leu Thr Arg Tyr Leu Arg Ile His Pro Gln Ile Trp Glu His Gln Ile 2290 2295 2300Ala Leu Arg Leu Glu Ile Leu Gly Cys Glu Ala Gln Gln Gln Tyr2305 2310 2315 29 6402 DNA Porcine CDS (1)..(6399) 29atg cag cta gag ctc tcc acc tgt gtc ttt ctg tgt ctc ttg cca ctc 48Met Gln Leu Glu Leu Ser Thr Cys Val Phe Leu Cys Leu Leu Pro Leu 1 5 10 15ggc ttt agt gcc atc agg aga tac tac ctg ggc gca gtg gaa ctg tcc 96Gly Phe Ser Ala Ile Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser 20 25 30tgg gac tac cgg caa agt gaa ctc ctc cgt gag ctg cac gtg gac acc 144Trp Asp Tyr Arg Gln Ser Glu Leu Leu Arg Glu Leu His Val Asp Thr 35 40 45aga ttt cct gct aca gcg cca gga gct ctt ccg ttg ggc ccg tca gtc 192Arg Phe Pro Ala Thr Ala Pro Gly Ala Leu Pro Leu Gly Pro Ser Val 50 55 60ctg tac aaa aag act gtg ttc gta gag ttc acg gat caa ctt ttc agc 240Leu Tyr Lys Lys Thr Val Phe Val Glu Phe Thr Asp Gln Leu Phe Ser 65 70 75 80gtt gcc agg ccc agg cca cca tgg atg ggt ctg ctg ggt cct acc atc 288Val Ala Arg Pro Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile 85 90 95cag gct gag gtt tac gac acg gtg gtc gtt acc ctg aag aac atg gct 336Gln Ala Glu Val Tyr Asp Thr Val Val Val Thr Leu Lys Asn Met Ala 100 105 110tct cat ccc gtt agt ctt cac gct gtc ggc gtc tcc ttc tgg aaa tct 384Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Phe Trp Lys Ser 115 120 125tcc gaa ggc gct gaa tat gag gat cac acc agc caa agg gag aag gaa 432Ser Glu Gly Ala Glu Tyr Glu Asp His Thr Ser Gln Arg Glu Lys Glu 130 135 140gac gat aaa gtc ctt ccc ggt aaa agc caa acc tac gtc tgg cag gtc 480Asp Asp Lys Val Leu Pro Gly Lys Ser Gln Thr Tyr Val Trp Gln Val145 150 155 160ctg aaa gaa aat ggt cca aca gcc tct gac cca cca tgt ctc acc tac 528Leu Lys Glu Asn Gly Pro Thr Ala Ser Asp Pro Pro Cys Leu Thr Tyr 165 170 175tca tac ctg tct cac gtg gac ctg gtg aaa gac ctg aat tcg ggc ctc 576Ser Tyr Leu Ser His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu 180 185 190att gga gcc ctg ctg gtt tgt aga gaa ggg agt ctg acc aga gaa agg 624Ile Gly Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Thr Arg Glu Arg 195 200 205acc cag aac ctg cac gaa ttt gta cta ctt ttt gct gtc ttt gat gaa 672Thr Gln Asn Leu His Glu Phe Val Leu Leu Phe Ala Val Phe Asp Glu 210 215 220ggg aaa agt tgg cac tca gca aga aat gac tcc tgg aca cgg gcc atg 720Gly Lys Ser Trp His Ser Ala Arg Asn Asp Ser Trp Thr Arg Ala Met225 230 235 240gat ccc gca cct gcc agg gcc cag cct gca atg cac aca gtc aat ggc 768Asp Pro Ala Pro Ala Arg Ala Gln Pro Ala Met His Thr Val Asn Gly 245 250 255tat gtc aac agg tct ctg cca ggt ctg atc gga tgt cat aag aaa tca 816Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His Lys Lys Ser 260 265 270gtc tac tgg cac gtg att gga atg ggc acc agc ccg gaa gtg cac tcc 864Val Tyr Trp His Val Ile Gly Met Gly Thr Ser Pro Glu Val His Ser 275 280 285att ttt ctt gaa ggc cac acg ttt ctc gtg agg cac cat cgc cag gct 912Ile Phe Leu Glu Gly His Thr Phe Leu Val Arg His His Arg Gln Ala 290 295 300tcc ttg gag atc tcg cca cta act ttc ctc act gct cag aca ttc ctg 960Ser Leu Glu Ile Ser Pro Leu Thr Phe Leu Thr Ala Gln Thr Phe Leu305 310 315 320atg gac ctt ggc cag ttc cta ctg ttt tgt cat atc tct tcc cac cac 1008Met Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser Ser His His 325 330 335cat ggt ggc atg gag gct cac gtc aga gta gaa agc tgc gcc gag gag 1056His Gly Gly Met Glu Ala His Val Arg Val Glu Ser Cys Ala Glu Glu 340 345 350ccc cag ctg cgg agg aaa gct gat gaa gag gaa gat tat gat gac aat 1104Pro Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu Asp Tyr Asp Asp Asn 355 360 365ttg tac gac tcg gac atg gac gtg gtc cgg ctc gat ggt gac gac gtg 1152Leu Tyr Asp Ser Asp Met Asp Val Val Arg Leu Asp Gly Asp Asp Val 370 375 380tct ccc ttt atc caa atc cgc tcg gtt gcc aag aag cat ccc aaa acc 1200Ser Pro Phe Ile Gln Ile Arg Ser Val Ala Lys Lys His Pro Lys Thr385 390 395 400tgg gtg cac tac atc tct gca gag gag gag gac tgg gac tac gcc ccc 1248Trp Val His Tyr Ile Ser Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro 405 410 415gcg gtc ccc agc ccc agt gac aga agt tat aaa agt ctc tac ttg aac 1296Ala Val Pro Ser Pro Ser Asp Arg Ser Tyr Lys Ser Leu Tyr Leu Asn 420 425 430agt ggt cct cag cga att ggt agg aaa tac aaa aaa gct cga ttc gtc 1344Ser Gly Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys Ala Arg Phe Val 435 440 445gct tac acg gat gta aca ttt aag act cgt aaa gct att ccg tat gaa 1392Ala Tyr Thr Asp Val Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr Glu 450 455 460tca gga atc ctg gga cct tta ctt tat gga gaa gtt gga gac aca ctt 1440Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu465 470 475 480ttg att ata ttt aag aat aaa gcg agc cga cca tat aac atc tac cct 1488Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro Tyr Asn Ile Tyr Pro 485 490 495cat gga atc act gat gtc agc gct ttg cac cca ggg aga ctt cta aaa 1536His Gly Ile Thr Asp Val Ser Ala Leu His Pro Gly Arg Leu Leu Lys 500 505 510ggt tgg aaa cat ttg aaa gac atg cca att ctg cca gga gag act ttc 1584Gly Trp Lys His Leu Lys Asp Met Pro Ile Leu Pro Gly Glu Thr Phe 515 520 525aag tat aaa tgg aca gtg act gtg gaa gat ggg cca acc aag tcc gat 1632Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp 530 535 540cct cgg tgc ctg acc cgc tac tac tcg agc tcc att aat cta gag aaa 1680Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Ser Ile Asn Leu Glu Lys545 550 555 560gat ctg gct tcg gga ctc att ggc cct ctc ctc atc tgc tac aaa gaa 1728Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu 565 570 575tct gta gac caa aga gga aac cag atg atg tca gac aag aga aac gtc 1776Ser Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn Val 580 585 590atc ctg ttt tct gta ttc gat gag aat caa agc tgg tac ctc gca gag 1824Ile Leu Phe Ser Val Phe Asp Glu Asn Gln Ser Trp Tyr Leu Ala Glu 595 600 605aat att cag cgc ttc ctc ccc aat ccg gat gga tta cag ccc cag gat 1872Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp Gly Leu Gln Pro Gln Asp 610 615 620cca gag ttc caa gct tct aac atc atg cac agc atc aat ggc tat gtt 1920Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val625 630 635 640ttt gat agc ttg cag ctg tcg gtt tgt ttg cac gag gtg gca tac tgg 1968Phe Asp Ser Leu Gln Leu Ser Val Cys Leu His Glu Val Ala Tyr Trp 645 650 655tac att cta agt gtt gga gca cag acg gac ttc ctc tcc gtc ttc ttc 2016Tyr Ile Leu Ser Val Gly Ala Gln Thr Asp Phe Leu Ser Val Phe Phe 660 665 670tct ggc tac acc ttc aaa cac aaa atg gtc tat gaa gac aca ctc acc 2064Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr 675 680 685ctg ttc ccc ttc tca gga gaa acg gtc ttc atg tca atg gaa aac cca 2112Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro 690 695 700ggt ctc tgg gtc cta ggg tgc cac aac tca gac ttg cgg aac aga ggg 2160Gly Leu Trp Val Leu Gly Cys His Asn Ser Asp Leu Arg Asn Arg Gly705 710 715 720atg aca gcc tta ctg aag gtg tat agt tgt gac agg gac att ggt gat 2208Met Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp Arg Asp Ile Gly Asp 725 730 735tat tat gac aac act tat gaa gat att cca ggc ttc ttg ctg agt gga 2256Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile Pro Gly Phe Leu Leu Ser Gly 740 745 750aag aat gtc att gaa ccc aga agc ttt gcc cag aat tca aga ccc cct 2304Lys Asn Val Ile Glu Pro Arg Ser Phe Ala Gln Asn Ser Arg Pro Pro 755 760 765agt gcg agc caa aag caa ttc caa acc atc aca agt cca gaa gat gac 2352Ser Ala Ser Gln Lys Gln Phe Gln Thr Ile Thr Ser Pro Glu Asp Asp 770 775 780gtg gag ctt gac ccg cag tct gga gag aga acc caa gca ctg gaa gaa 2400Val Glu Leu Asp Pro Gln Ser Gly Glu Arg Thr Gln Ala Leu Glu Glu785 790 795 800cta agt gtc ccc tct ggt gat ggg tcg atg ctc ttg gga cag aat cct 2448Leu Ser Val Pro Ser Gly Asp Gly Ser Met Leu Leu Gly Gln Asn Pro 805 810 815gct cca cat ggc tca tcc tca tct gat ctt caa gaa gcc agg aat gag 2496Ala Pro His Gly Ser Ser Ser Ser Asp Leu Gln Glu Ala Arg Asn Glu 820 825 830gct gat gat tat tta cct gga gca aga gaa aga ggc acg gcc cca tcc 2544Ala Asp Asp Tyr Leu Pro Gly Ala Arg Glu Arg Gly Thr Ala Pro Ser 835 840 845gca gcg gca cgt ctc aga cca gag ctg cat cac agt gcc gaa aga gta 2592Ala Ala Ala Arg Leu Arg Pro Glu Leu His His Ser Ala Glu Arg Val 850 855 860ctt act cct gag cca gag aaa gag ttg aag aaa ctt gat tca aaa atg 2640Leu Thr Pro Glu Pro Glu Lys Glu Leu Lys Lys Leu Asp Ser Lys Met865 870 875 880tct agt tca tca gac ctt cta aag act tcg cca aca att cca tca gac 2688Ser Ser Ser Ser Asp Leu Leu Lys Thr Ser Pro Thr Ile Pro Ser Asp 885 890 895acg ttg tca gcg gag act gaa agg aca cat tcc tta ggc ccc cca cac 2736Thr Leu Ser Ala Glu Thr Glu Arg Thr His Ser Leu Gly Pro Pro His 900 905 910ccg cag gtt aat ttc agg agt caa tta ggt gcc att gta ctt ggc aaa 2784Pro Gln Val Asn Phe Arg Ser Gln Leu Gly Ala Ile Val Leu Gly Lys 915 920 925aat tca tct cac ttt att ggg gct ggt gtc cct ttg ggc tcg act gag 2832Asn Ser Ser His Phe Ile Gly Ala Gly Val Pro Leu Gly Ser Thr Glu 930 935 940gag gat cat gaa agc tcc ctg gga gaa aat gta tca cca gtg gag agt 2880Glu Asp His Glu Ser Ser Leu Gly Glu Asn Val Ser Pro Val Glu Ser945 950 955 960gac ggg ata ttt gaa aag gaa aga gct cat gga cct gct tca ctg acc 2928Asp Gly Ile Phe Glu Lys Glu Arg Ala His Gly Pro Ala Ser Leu Thr 965 970 975aaa gac gat gtt tta ttt aaa gtt aat atc tct ttg gta aag aca aac 2976Lys Asp Asp Val Leu Phe Lys Val Asn Ile Ser Leu Val Lys Thr Asn 980 985 990aag gca cga gtt tac tta aaa act aat aga aag att cac att gat gac 3024Lys Ala Arg Val Tyr Leu Lys Thr Asn Arg Lys Ile His Ile Asp Asp 995 1000 1005gca gct tta tta act gag aat agg gca tct gca acg ttt atg gac aaa 3072Ala Ala Leu Leu Thr Glu Asn Arg Ala Ser Ala Thr Phe Met Asp Lys 1010 1015 1020aat act aca gct tcg gga tta aat cat gtg tca aat tgg ata aaa ggg 3120Asn Thr Thr Ala Ser Gly Leu Asn His Val Ser Asn Trp Ile Lys Gly1025 1030 1035 1040ccc ctt ggc aag aac ccc cta agc tcg gag cga ggc ccc agt cca gag 3168Pro Leu Gly Lys Asn Pro Leu Ser Ser Glu Arg Gly Pro Ser Pro Glu 1045 1050 1055ctt ctg aca tct tca gga tca gga aaa tct gtg aaa ggt cag agt tct 3216Leu Leu Thr Ser Ser Gly Ser Gly Lys Ser Val Lys Gly Gln Ser Ser 1060 1065 1070ggg cag ggg aga ata cgg gtg gca gtg gaa gag gaa gaa ctg agc aaa 3264Gly Gln Gly Arg Ile Arg Val Ala Val Glu Glu Glu Glu Leu Ser Lys 1075 1080 1085ggc aaa gag atg atg ctt ccc aac agc gag ctc acc ttt ctc act aac 3312Gly Lys Glu Met Met Leu Pro Asn Ser Glu Leu Thr Phe Leu Thr Asn 1090 1095 1100tcg gct gat gtc caa gga aac gat aca cac agt caa gga aaa aag tct 3360Ser Ala Asp Val Gln Gly Asn Asp Thr His Ser Gln Gly Lys Lys Ser1105 1110 1115 1120cgg gaa gag atg gaa agg aga gaa aaa tta gtc caa gaa aaa gtc gac 3408Arg Glu Glu Met Glu Arg Arg Glu Lys Leu Val Gln Glu Lys Val Asp 1125 1130 1135ttg cct cag gtg tat aca gcg act gga act aag aat ttc ctg aga aac 3456Leu Pro Gln Val Tyr Thr Ala Thr Gly Thr Lys Asn Phe Leu Arg Asn 1140 1145 1150att ttt cac caa agc act gag ccc agt gta gaa ggg ttt gat ggg ggg 3504Ile Phe His Gln Ser Thr Glu Pro Ser Val Glu Gly Phe Asp Gly Gly 1155 1160 1165tca cat gcg ccg gtg cct caa gac agc agg tca tta aat gat tcg gca 3552Ser His Ala Pro Val Pro Gln Asp Ser Arg Ser Leu Asn Asp Ser Ala 1170 1175 1180gag aga gca gag act cac ata gcc cat ttc tca gca att agg gaa gag 3600Glu Arg Ala Glu Thr His Ile Ala His Phe Ser Ala Ile Arg Glu Glu1185 1190 1195 1200gca ccc ttg gaa gcc ccg gga aat cga aca ggt cca ggt ccg agg agt 3648Ala Pro Leu Glu Ala Pro Gly Asn Arg Thr Gly Pro Gly Pro Arg Ser 1205 1210 1215gcg gtt ccc cgc cgc gtt aag cag agc ttg aaa cag atc aga ctc ccg 3696Ala Val Pro Arg Arg Val Lys Gln Ser Leu Lys Gln Ile Arg Leu Pro 1220 1225 1230cta gaa gaa ata aag cct gaa agg ggg gtg gtt ctg aat gcc acc tca 3744Leu Glu Glu Ile Lys Pro Glu Arg Gly Val Val Leu Asn Ala Thr Ser 1235 1240 1245acc cgg tgg tct gaa agc agt cct atc tta caa gga gcc aaa aga aat 3792Thr Arg Trp Ser Glu Ser Ser Pro Ile Leu Gln Gly Ala Lys Arg Asn 1250 1255 1260aac ctt tct tta cct ttc ctg acc ttg gaa atg gcc gga ggt caa gga 3840Asn Leu Ser Leu Pro Phe Leu Thr Leu Glu Met Ala Gly Gly Gln Gly1265 1270 1275 1280aag atc agc gcc ctg ggg aaa agt gcc gca ggc ccg ctg gcg tcc ggg 3888Lys Ile Ser Ala Leu Gly Lys Ser Ala Ala Gly Pro Leu Ala Ser Gly 1285 1290 1295aag ctg gag aag gct gtt ctc tct tca gca ggc ttg tct gaa gca tct 3936Lys Leu Glu Lys Ala Val Leu Ser Ser Ala Gly Leu Ser Glu Ala Ser 1300 1305 1310ggc aaa gct gag ttt ctt cct aaa gtt cga gtt cat cgg gaa gac ctg 3984Gly Lys Ala Glu Phe Leu Pro Lys Val Arg Val His Arg Glu Asp Leu 1315 1320 1325ttg cct caa aaa acc agc aat gtt tct tgc gca cac ggg gat ctc ggc 4032Leu Pro Gln Lys Thr Ser Asn Val Ser Cys Ala His Gly Asp Leu Gly 1330 1335 1340cag gag atc ttc ctg cag aaa aca cgg gga cct gtt aac ctg aac aaa 4080Gln Glu Ile Phe Leu Gln Lys Thr Arg Gly Pro Val Asn Leu Asn Lys1345 1350 1355 1360gta aat aga cct gga agg act ccc tcc aag ctt ctg ggt ccc ccg atg 4128Val Asn Arg Pro Gly Arg Thr Pro Ser Lys Leu Leu Gly Pro Pro Met 1365 1370 1375ccc aaa gag tgg gaa tcc cta gag aag tca cca aaa agc aca gct ctc 4176Pro Lys Glu Trp Glu Ser Leu Glu Lys Ser Pro Lys Ser Thr Ala Leu 1380 1385 1390agg acg aaa gac atc atc agt tta ccc ctg gac cgt cac gaa agc aat 4224Arg Thr Lys Asp Ile Ile Ser Leu Pro Leu Asp Arg His Glu Ser Asn 1395 1400 1405cat tca ata gca gca aaa aat gaa gga caa gcc gag acc caa aga gaa 4272His Ser Ile Ala Ala Lys Asn Glu Gly Gln Ala Glu Thr Gln Arg Glu 1410 1415 1420gcc gcc tgg acg aag cag gga ggg cct gga agg ctg tgc gct cca aag 4320Ala Ala Trp Thr Lys Gln Gly Gly Pro Gly Arg Leu Cys Ala Pro Lys1425 1430 1435 1440cct ccg gtc ctg cga cgg cat cag agg gac ata agc ctt cct act ttt 4368Pro Pro Val Leu Arg Arg His Gln Arg Asp Ile Ser Leu Pro Thr Phe 1445 1450 1455cag ccg gag gaa gac aaa atg gac tat gat gat atc ttc tca act gaa 4416Gln Pro Glu Glu Asp Lys Met Asp Tyr Asp Asp Ile Phe Ser Thr Glu 1460 1465 1470acg aag gga gaa gat ttt gac att tac ggt gag gat gaa aat cag gac 4464Thr Lys Gly Glu Asp Phe Asp Ile Tyr Gly Glu Asp Glu Asn Gln Asp 1475 1480 1485cct cgc agc ttt cag aag aga acc cga cac tat ttc att gct gcg gtg 4512Pro Arg Ser Phe Gln Lys Arg Thr Arg His Tyr Phe Ile Ala Ala Val 1490 1495 1500gag cag ctc tgg gat tac ggg atg agc gaa tcc ccc cgg gcg cta aga 4560Glu Gln Leu Trp Asp Tyr Gly Met Ser Glu Ser Pro Arg Ala Leu Arg1505 1510 1515 1520aac agg gct cag aac gga gag gtg cct cgg ttc aag aag gtg gtc ttc 4608Asn Arg Ala Gln Asn Gly Glu Val Pro Arg Phe Lys Lys Val Val Phe 1525 1530 1535cgg gaa ttt gct gac ggc tcc ttc acg cag ccg tcg tac cgc ggg gaa 4656Arg Glu Phe Ala Asp Gly Ser Phe Thr Gln Pro Ser Tyr Arg Gly Glu 1540 1545 1550ctc aac aaa cac ttg ggg ctc ttg gga ccc tac atc aga gcg gaa gtt 4704Leu Asn Lys His Leu Gly Leu Leu Gly Pro Tyr Ile Arg Ala Glu Val 1555 1560 1565gaa gac aac atc atg gta act ttc aaa aac cag gcg tct cgt ccc tat 4752Glu Asp Asn Ile Met Val Thr Phe Lys Asn Gln Ala Ser Arg Pro Tyr 1570 1575 1580tcc ttc tac tcg agc ctt att tct tat ccg gat gat cag gag caa ggg 4800Ser Phe Tyr Ser Ser Leu Ile Ser Tyr Pro Asp Asp Gln Glu Gln Gly1585 1590 1595 1600gca gaa cct cga cac aac ttc gtc cag cca aat gaa acc aga act tac 4848Ala Glu Pro Arg His Asn Phe Val Gln Pro Asn Glu Thr Arg Thr Tyr 1605 1610 1615ttt tgg aaa gtg cag cat cac atg gca ccc aca gaa gac gag ttt gac 4896Phe Trp Lys Val Gln His His Met Ala Pro Thr Glu Asp Glu Phe Asp 1620 1625 1630tgc aaa gcc tgg gcc tac ttt tct gat gtt gac ctg gaa aaa gat gtg 4944Cys Lys Ala Trp Ala Tyr Phe Ser Asp Val Asp Leu Glu Lys Asp Val 1635 1640 1645cac tca ggc ttg atc ggc ccc ctt ctg atc tgc cgc gcc aac acc ctg 4992His Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Arg Ala Asn Thr Leu 1650 1655 1660aac gct gct cac ggt aga caa gtg acc gtg caa gaa ttt gct ctg ttt 5040Asn Ala Ala His Gly Arg Gln Val Thr Val Gln Glu Phe Ala Leu Phe1665 1670 1675 1680ttc act att ttt gat gag aca aag agc tgg tac ttc act gaa aat gtg 5088Phe Thr Ile Phe Asp Glu Thr Lys Ser Trp Tyr Phe Thr Glu Asn Val 1685 1690 1695gaa agg aac tgc cgg gcc ccc tgc cac ctg cag atg gag gac ccc act 5136Glu Arg Asn Cys Arg Ala Pro Cys His Leu Gln Met Glu Asp Pro Thr 1700 1705 1710ctg aaa gaa aac tat cgc ttc cat gca atc aat ggc tat gtg atg gat 5184Leu Lys Glu Asn Tyr Arg Phe His Ala Ile Asn Gly Tyr Val Met Asp 1715 1720 1725aca ctc cct ggc tta gta atg gct cag aat caa agg atc cga tgg tat 5232Thr Leu Pro Gly Leu Val Met Ala Gln Asn Gln Arg Ile Arg Trp Tyr 1730 1735 1740ctg ctc agc atg ggc agc aat gaa aat atc cat tcg att cat ttt agc 5280Leu Leu Ser Met Gly Ser Asn Glu Asn Ile His Ser Ile His Phe Ser1745 1750 1755 1760gga cac gtg ttc agt gta cgg aaa aag gag gag tat aaa atg gcc gtg 5328Gly His Val Phe Ser Val Arg Lys Lys Glu Glu Tyr Lys Met Ala Val 1765 1770 1775tac aat ctc tat ccg ggt gtc ttt gag aca gtg gaa atg cta ccg tcc 5376Tyr Asn Leu Tyr Pro Gly Val Phe Glu Thr Val Glu Met Leu Pro Ser 1780 1785 1790aaa gtt gga att tgg cga ata gaa tgc ctg att ggc gag cac ctg caa 5424Lys Val Gly Ile Trp Arg Ile Glu Cys Leu Ile Gly Glu His Leu Gln 1795 1800 1805gct ggg atg agc acg act ttc ctg gtg tac agc aag gag tgt cag gct 5472Ala Gly Met Ser Thr Thr Phe Leu Val Tyr Ser Lys Glu Cys Gln Ala 1810 1815 1820cca ctg gga atg gct tct gga cgc att aga gat ttt cag atc aca gct 5520Pro Leu Gly Met Ala Ser Gly Arg Ile Arg Asp Phe Gln Ile Thr Ala1825 1830 1835 1840tca gga cag tat gga cag tgg gcc cca aag ctg gcc aga ctt cat tat 5568Ser Gly Gln Tyr Gly Gln Trp Ala Pro Lys Leu Ala Arg Leu His Tyr 1845 1850 1855tcc gga tca atc aat gcc tgg agc acc aag gat ccc cac tcc tgg atc 5616Ser Gly Ser Ile Asn Ala Trp Ser Thr Lys Asp Pro His Ser Trp Ile 1860 1865 1870aag gtg gat ctg ttg gca cca atg atc att cac ggc atc atg acc cag 5664Lys Val Asp Leu Leu Ala Pro Met Ile Ile His Gly Ile Met Thr Gln 1875 1880 1885ggt gcc cgt cag aag ttt tcc agc ctc tac atc tcc cag ttt atc atc 5712Gly Ala Arg Gln Lys Phe Ser Ser Leu Tyr Ile Ser Gln Phe Ile Ile 1890 1895 1900atg tac agt ctt gac ggg agg aac tgg cag agt tac cga ggg aat tcc 5760Met Tyr Ser Leu Asp Gly Arg Asn Trp Gln Ser Tyr Arg Gly Asn Ser1905 1910 1915 1920acg ggc acc tta atg gtc ttc ttt ggc aat gtg gac gca tct ggg att 5808Thr Gly Thr Leu Met Val Phe Phe Gly Asn Val Asp Ala Ser Gly Ile 1925 1930 1935aaa cac aat att ttt aac cct ccg att gtg gct cgg tac atc cgt ttg 5856Lys His Asn Ile Phe Asn Pro Pro Ile Val Ala Arg Tyr Ile Arg Leu 1940 1945 1950cac cca aca cat tac agc atc cgc agc act ctt cgc atg gag ttg atg 5904His Pro Thr His Tyr Ser Ile Arg Ser Thr Leu Arg Met Glu Leu Met 1955 1960 1965ggc tgt gat tta aac agt tgc agc atg ccc ctg gga atg cag aat aaa 5952Gly Cys Asp Leu Asn Ser Cys Ser Met Pro Leu Gly Met Gln Asn Lys 1970 1975 1980gcg ata tca gac tca cag atc acg gcc tcc tcc cac cta agc aat ata 6000Ala Ile Ser Asp Ser Gln Ile Thr Ala Ser Ser His Leu Ser Asn Ile1985 1990 1995 2000ttt gcc acc tgg tct cct tca caa gcc cga ctt cac ctc cag ggg cgg 6048Phe Ala Thr Trp Ser Pro Ser Gln Ala Arg Leu His Leu Gln Gly Arg 2005 2010 2015acg aat gcc tgg cga ccc cgg gtg agc agc gca gag gag tgg ctg cag 6096Thr Asn Ala Trp Arg Pro Arg Val Ser Ser Ala Glu Glu Trp Leu Gln 2020 2025 2030gtg gac ctg cag aag acg gtg aag gtc aca ggc atc acc acc cag ggc 6144Val Asp Leu Gln Lys Thr Val Lys Val Thr Gly Ile Thr Thr Gln Gly 2035 2040 2045gtg aag tcc ctg ctc agc agc atg tat gtg aag gag ttc ctc gtg tcc 6192Val Lys Ser Leu Leu Ser Ser Met Tyr Val Lys Glu Phe Leu Val Ser 2050 2055 2060agt agt cag gac ggc cgc cgc tgg acc ctg ttt ctt cag gac ggc cac 6240Ser Ser Gln Asp Gly Arg Arg Trp Thr Leu Phe Leu Gln Asp Gly His2065 2070 2075 2080acg aag gtt ttt cag ggc aat cag gac tcc tcc acc ccc gtg gtg aac 6288Thr Lys Val Phe Gln Gly Asn Gln Asp Ser Ser Thr Pro Val Val Asn 2085 2090 2095gct ctg gac ccc ccg ctg ttc acg cgc tac ctg agg atc cac ccc acg 6336Ala Leu Asp Pro Pro Leu Phe Thr Arg Tyr Leu Arg Ile His Pro Thr 2100 2105 2110agc tgg gcg cag cac atc gcc ctg agg ctc gag gtt cta gga tgt gag 6384Ser Trp Ala Gln His Ile Ala Leu Arg Leu Glu Val Leu Gly Cys Glu 2115 2120 2125gca cag gat ctc tac tga 6402Ala Gln Asp Leu Tyr 2130 30 2133 PRT Porcine 30Met Gln Leu Glu Leu Ser Thr Cys Val Phe Leu Cys Leu Leu Pro Leu 1 5 10 15Gly Phe Ser Ala Ile Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser 20 25 30Trp Asp Tyr Arg Gln Ser Glu Leu Leu Arg Glu Leu His Val Asp Thr 35 40 45Arg Phe Pro Ala Thr Ala Pro Gly Ala Leu Pro Leu Gly Pro Ser Val 50 55 60Leu Tyr Lys Lys Thr Val Phe Val Glu Phe Thr Asp Gln Leu Phe Ser 65 70 75 80Val Ala Arg Pro Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile 85 90 95Gln Ala Glu Val Tyr Asp Thr Val Val Val Thr Leu Lys Asn Met Ala 100 105 110Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Phe Trp Lys Ser 115 120 125Ser Glu Gly Ala Glu Tyr Glu Asp His Thr Ser Gln Arg Glu Lys Glu 130 135 140Asp Asp Lys Val Leu Pro Gly Lys Ser Gln Thr Tyr Val Trp Gln Val145 150 155 160Leu Lys Glu Asn Gly Pro Thr Ala Ser Asp Pro Pro Cys Leu Thr Tyr 165 170 175Ser Tyr Leu Ser His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu 180 185 190Ile Gly Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Thr Arg Glu Arg 195 200 205Thr Gln Asn Leu His Glu Phe Val Leu Leu Phe Ala Val Phe Asp Glu 210 215 220Gly Lys Ser Trp His Ser Ala Arg Asn Asp Ser Trp Thr Arg Ala Met225 230 235 240Asp Pro Ala Pro Ala Arg Ala Gln Pro Ala Met His Thr Val Asn Gly 245 250 255Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His Lys Lys Ser 260 265 270Val Tyr Trp His Val Ile Gly Met Gly Thr Ser Pro Glu Val His Ser 275 280 285Ile Phe Leu Glu Gly His Thr Phe Leu Val Arg His His Arg Gln Ala 290 295 300Ser Leu Glu Ile Ser Pro Leu Thr Phe Leu Thr Ala Gln Thr Phe Leu305 310 315 320Met Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser Ser His His 325 330 335His Gly Gly Met Glu Ala His Val Arg Val Glu Ser Cys Ala Glu Glu 340 345 350Pro Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu Asp Tyr Asp Asp Asn 355 360 365Leu Tyr Asp Ser Asp Met Asp Val Val Arg Leu Asp Gly Asp Asp Val 370 375 380Ser Pro Phe Ile Gln Ile Arg Ser Val Ala Lys Lys His Pro Lys Thr385 390 395 400Trp Val His Tyr Ile Ser Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro 405 410 415Ala Val Pro Ser Pro Ser Asp Arg Ser Tyr Lys Ser Leu Tyr Leu Asn 420 425 430Ser Gly Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys Ala Arg Phe Val 435 440 445Ala Tyr Thr Asp Val Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr Glu 450 455 460Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu465 470 475 480Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro Tyr Asn Ile Tyr Pro 485 490 495His Gly Ile Thr Asp Val Ser Ala Leu His Pro Gly Arg Leu Leu Lys 500 505 510Gly Trp Lys His Leu Lys Asp Met Pro Ile Leu Pro Gly Glu Thr Phe 515 520 525Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp 530 535 540Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Ser Ile Asn Leu Glu Lys545 550 555 560Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu 565 570 575Ser Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn Val 580 585 590Ile Leu Phe Ser Val Phe Asp Glu Asn Gln Ser Trp Tyr Leu Ala Glu 595 600 605Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp Gly Leu Gln Pro Gln Asp 610 615 620Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val625 630 635 640Phe Asp Ser Leu Gln Leu Ser Val Cys Leu His Glu Val Ala Tyr Trp 645 650 655Tyr Ile Leu Ser Val Gly Ala Gln Thr Asp Phe Leu Ser Val Phe Phe 660 665 670Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr 675 680 685Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro 690 695 700Gly Leu Trp Val Leu Gly Cys His Asn Ser Asp Leu Arg Asn Arg Gly705 710 715 720Met Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp Arg Asp Ile Gly Asp 725 730 735Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile Pro Gly Phe Leu Leu Ser Gly 740 745 750Lys Asn Val Ile Glu Pro Arg Ser Phe Ala Gln Asn Ser Arg Pro Pro 755 760 765Ser Ala Ser Gln Lys Gln Phe Gln Thr Ile Thr Ser Pro Glu Asp Asp 770 775 780Val Glu Leu Asp Pro Gln Ser Gly Glu Arg Thr Gln Ala Leu Glu Glu785 790 795 800Leu Ser Val Pro Ser Gly Asp Gly Ser Met Leu Leu Gly Gln Asn Pro 805 810 815Ala Pro His Gly Ser Ser Ser Ser Asp Leu Gln Glu Ala Arg Asn Glu 820 825 830Ala Asp Asp Tyr Leu Pro Gly Ala Arg Glu Arg Gly Thr Ala Pro Ser 835 840 845Ala Ala Ala Arg Leu Arg Pro Glu Leu His His Ser Ala Glu Arg Val 850 855 860Leu Thr Pro Glu Pro Glu Lys Glu Leu Lys Lys Leu Asp Ser Lys Met865 870 875 880Ser Ser Ser Ser Asp Leu Leu Lys Thr Ser Pro Thr Ile Pro Ser Asp 885 890 895Thr Leu Ser Ala Glu Thr Glu Arg Thr His Ser Leu Gly Pro Pro His 900 905 910Pro Gln Val Asn Phe Arg Ser Gln Leu Gly Ala Ile Val Leu Gly Lys 915 920 925Asn Ser Ser His Phe Ile Gly Ala Gly Val Pro Leu Gly Ser Thr Glu 930 935 940Glu Asp His Glu Ser Ser Leu Gly Glu Asn Val Ser Pro Val Glu Ser945 950 955 960Asp Gly Ile Phe Glu Lys Glu Arg Ala His Gly Pro Ala Ser Leu Thr 965 970 975Lys Asp Asp Val Leu Phe Lys Val Asn Ile Ser Leu Val Lys Thr Asn 980 985 990Lys Ala Arg Val Tyr Leu Lys Thr Asn Arg Lys Ile His Ile Asp Asp 995 1000 1005Ala Ala Leu Leu Thr Glu Asn Arg Ala Ser Ala Thr Phe Met Asp Lys 1010 1015 1020Asn Thr Thr Ala Ser Gly Leu Asn His Val Ser Asn Trp Ile Lys Gly1025 1030 1035 1040Pro Leu Gly Lys Asn Pro Leu Ser Ser Glu Arg Gly Pro Ser Pro Glu 1045 1050 1055Leu Leu Thr Ser Ser Gly Ser Gly Lys Ser Val Lys Gly Gln Ser Ser 1060 1065 1070Gly Gln Gly Arg Ile Arg Val Ala Val Glu Glu Glu Glu Leu Ser Lys 1075 1080 1085Gly Lys Glu Met Met Leu Pro Asn Ser Glu Leu Thr Phe Leu Thr Asn 1090 1095 1100Ser Ala Asp Val Gln Gly Asn Asp Thr His Ser Gln Gly Lys Lys Ser1105 1110 1115 1120Arg Glu Glu Met Glu Arg Arg Glu Lys Leu Val Gln Glu Lys Val Asp 1125 1130 1135Leu Pro Gln Val Tyr Thr Ala Thr Gly Thr Lys Asn Phe Leu Arg Asn 1140 1145 1150Ile Phe His Gln Ser Thr Glu Pro Ser Val Glu Gly Phe Asp Gly Gly 1155 1160 1165Ser His Ala Pro Val Pro Gln Asp Ser Arg Ser Leu Asn Asp Ser Ala 1170 1175 1180Glu Arg Ala Glu Thr His Ile Ala His Phe Ser Ala Ile Arg Glu Glu1185 1190 1195 1200Ala Pro Leu Glu Ala Pro Gly Asn Arg Thr Gly Pro Gly Pro Arg Ser 1205 1210 1215Ala Val Pro Arg Arg Val Lys Gln Ser Leu Lys Gln Ile Arg Leu Pro 1220 1225 1230Leu Glu Glu Ile Lys Pro Glu Arg Gly Val Val Leu Asn Ala Thr Ser 1235 1240 1245Thr Arg Trp Ser Glu Ser Ser Pro Ile Leu Gln Gly Ala Lys Arg Asn 1250 1255 1260Asn Leu Ser Leu Pro Phe Leu Thr Leu Glu Met Ala Gly Gly Gln Gly1265 1270 1275 1280Lys Ile Ser Ala Leu Gly Lys Ser Ala Ala Gly Pro Leu Ala Ser Gly 1285 1290 1295Lys Leu Glu Lys Ala Val Leu Ser Ser Ala Gly Leu Ser Glu Ala Ser 1300 1305 1310Gly Lys Ala Glu Phe Leu Pro Lys Val Arg Val His Arg Glu Asp Leu 1315 1320 1325Leu Pro Gln Lys Thr Ser Asn Val Ser Cys Ala His Gly Asp Leu Gly 1330 1335 1340Gln Glu Ile Phe Leu Gln Lys Thr Arg Gly Pro Val Asn Leu Asn Lys1345 1350 1355 1360Val Asn Arg Pro Gly Arg Thr Pro Ser Lys Leu Leu Gly Pro Pro Met 1365 1370 1375Pro Lys Glu Trp Glu Ser Leu Glu Lys Ser Pro Lys Ser Thr Ala Leu 1380 1385 1390Arg Thr Lys Asp Ile Ile Ser Leu Pro Leu Asp Arg His Glu Ser Asn 1395 1400 1405His Ser Ile Ala Ala Lys Asn Glu Gly Gln Ala Glu Thr Gln Arg Glu 1410 1415 1420Ala Ala Trp Thr Lys Gln Gly Gly Pro Gly Arg Leu Cys Ala Pro Lys1425 1430 1435 1440Pro Pro Val Leu Arg Arg His Gln Arg Asp Ile Ser Leu Pro Thr Phe 1445 1450 1455Gln Pro Glu Glu Asp Lys Met Asp Tyr Asp Asp Ile Phe Ser Thr Glu 1460 1465 1470Thr Lys Gly Glu Asp Phe Asp Ile Tyr Gly Glu Asp Glu Asn Gln Asp 1475 1480 1485Pro Arg Ser Phe Gln Lys Arg Thr Arg His Tyr Phe Ile Ala Ala Val 1490 1495 1500Glu Gln Leu Trp Asp Tyr Gly Met Ser Glu Ser Pro Arg Ala Leu Arg1505 1510 1515 1520Asn Arg Ala Gln Asn Gly Glu Val Pro Arg Phe Lys Lys Val Val Phe 1525 1530 1535Arg Glu Phe Ala Asp Gly Ser Phe Thr Gln Pro Ser Tyr Arg Gly Glu 1540 1545 1550Leu Asn Lys His Leu Gly Leu Leu Gly Pro Tyr Ile Arg Ala Glu Val 1555 1560 1565Glu Asp Asn Ile Met Val Thr Phe Lys Asn Gln Ala Ser Arg Pro Tyr 1570 1575 1580Ser Phe Tyr Ser Ser Leu Ile Ser Tyr Pro Asp Asp Gln Glu Gln Gly1585 1590 1595 1600Ala Glu Pro Arg His Asn Phe Val Gln Pro Asn Glu Thr Arg Thr Tyr 1605 1610 1615Phe Trp Lys Val Gln His His Met Ala Pro Thr Glu Asp Glu Phe Asp 1620 1625 1630Cys Lys Ala Trp Ala Tyr Phe Ser Asp Val Asp Leu Glu Lys Asp Val 1635 1640 1645His Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Arg Ala Asn Thr Leu 1650 1655 1660Asn Ala Ala His Gly Arg Gln Val Thr Val Gln Glu Phe Ala Leu Phe1665 1670 1675 1680Phe Thr Ile Phe Asp Glu Thr Lys Ser Trp Tyr Phe Thr Glu Asn Val 1685 1690 1695Glu Arg Asn Cys Arg Ala Pro Cys His Leu Gln Met Glu Asp Pro Thr 1700 1705 1710Leu Lys Glu Asn Tyr Arg Phe His Ala Ile Asn Gly Tyr Val Met Asp 1715 1720 1725Thr Leu Pro Gly Leu Val Met Ala Gln Asn Gln Arg Ile Arg Trp Tyr 1730 1735 1740Leu Leu Ser Met Gly Ser Asn Glu Asn Ile His Ser Ile His Phe Ser1745 1750 1755 1760Gly His Val Phe Ser Val Arg Lys Lys Glu Glu Tyr Lys Met Ala Val 1765 1770 1775Tyr Asn Leu Tyr Pro Gly Val Phe Glu Thr Val Glu Met Leu Pro Ser 1780 1785 1790Lys Val Gly Ile Trp Arg Ile Glu Cys Leu Ile Gly Glu His Leu Gln 1795 1800 1805Ala Gly Met Ser Thr Thr Phe Leu Val Tyr Ser Lys Glu Cys Gln Ala 1810 1815 1820Pro Leu Gly Met Ala Ser Gly Arg Ile Arg Asp Phe Gln Ile Thr Ala1825 1830 1835 1840Ser Gly Gln Tyr Gly Gln Trp Ala Pro Lys Leu Ala Arg Leu His Tyr 1845 1850 1855Ser Gly Ser Ile Asn Ala Trp Ser Thr Lys Asp Pro His Ser Trp Ile 1860 1865 1870Lys Val Asp Leu Leu Ala Pro Met Ile Ile His Gly Ile Met Thr Gln 1875 1880 1885Gly Ala Arg Gln Lys Phe Ser Ser Leu Tyr Ile Ser Gln Phe Ile Ile 1890 1895 1900Met Tyr Ser Leu Asp Gly Arg Asn Trp Gln Ser Tyr Arg Gly Asn Ser1905 1910 1915 1920Thr Gly Thr Leu Met Val Phe Phe Gly Asn Val Asp Ala Ser Gly Ile 1925 1930 1935Lys His Asn Ile Phe Asn Pro Pro Ile Val Ala Arg Tyr Ile Arg Leu 1940 1945 1950His Pro Thr His Tyr Ser Ile Arg Ser Thr Leu Arg Met Glu Leu Met 1955 1960 1965Gly Cys Asp Leu Asn Ser Cys Ser Met Pro Leu Gly Met Gln Asn Lys 1970 1975 1980Ala Ile Ser Asp Ser Gln Ile Thr Ala Ser Ser His Leu Ser Asn Ile1985 1990 1995 2000Phe Ala Thr Trp Ser Pro Ser Gln Ala Arg Leu His Leu Gln Gly Arg 2005 2010 2015Thr Asn Ala Trp Arg Pro Arg Val Ser Ser Ala Glu Glu Trp Leu Gln 2020 2025 2030Val Asp Leu Gln Lys Thr Val Lys Val Thr Gly Ile Thr Thr Gln Gly 2035 2040 2045Val Lys Ser Leu Leu Ser Ser Met Tyr Val Lys Glu Phe Leu Val Ser 2050 2055 2060Ser Ser Gln Asp Gly Arg Arg Trp Thr Leu Phe Leu Gln Asp Gly His2065 2070 2075 2080Thr Lys Val Phe Gln Gly Asn Gln Asp Ser Ser Thr Pro Val Val Asn 2085 2090 2095Ala Leu Asp Pro Pro Leu Phe Thr Arg Tyr Leu Arg Ile His Pro Thr 2100 2105 2110Ser Trp Ala Gln His Ile Ala Leu Arg Leu Glu Val Leu Gly Cys Glu 2115 2120 2125Ala Gln Asp Leu Tyr 2130 31 19 PRT Homo sapiens 31Met Gln Ile Glu Leu Ser Thr Cys Phe Phe Leu Cys Leu Leu Arg Phe 1 5 10 15Cys Phe Ser 32 24 PRT Artificial Sequence Description of Artificial Sequencelinker 32Ser Phe Ala Gln Asn Ser Arg Pro Pro Ser Ala Ser Ala Pro Lys Pro 1 5 10 15Pro Val Leu Arg Arg His Gln Arg 20 33 105 DNA Artificial Sequence Description of Artificial Sequencelinker 33gtcattgaac ctaggagctt tgcccagaat tcaagacccc ctagtgcgag cgctccaaag 60cctccggtcc tgcgacggca tcagagggac ataagccttc ctact 105 34 21 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 34gaggaaaacc agatgatgtc a 21 35 60 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 35ctttggagcg ctcgcactag ggggtcttga attctgggca aagctcctag gttcaatgac 60 36 66 DNA Artificial Sequence Description of Artificial Sequence oligonucleotide primer 36cctagtgcga gcgctccaaa gcctccggtc ctgcgacggc atcagaggga cataagcctt 60cctact 66 37 4404 DNA Porcine CDS (1)..(4401) 37atg cag cta gag ctc tcc acc tgt gtc ttt ctg tgt ctc ttg cca ctc 48Met Gln Leu Glu Leu Ser Thr Cys Val Phe Leu Cys Leu Leu Pro Leu 1 5 10 15ggc ttt agt gcc atc agg aga tac tac ctg ggc gca gtg gaa ctg tcc 96Gly Phe Ser Ala Ile Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser 20 25 30tgg gac tac cgg caa agt gaa ctc ctc cgt gag ctg cac gtg gac acc 144Trp Asp Tyr Arg Gln Ser Glu Leu Leu Arg Glu Leu His Val Asp Thr 35 40 45aga ttt cct gct aca gcg cca gga gct ctt ccg ttg ggc ccg tca gtc 192Arg Phe Pro Ala Thr Ala Pro Gly Ala Leu Pro Leu Gly Pro Ser Val 50 55 60ctg tac aaa aag act gtg ttc gta gag ttc acg gat caa ctt ttc agc 240Leu Tyr Lys Lys Thr Val Phe Val Glu Phe Thr Asp Gln Leu Phe Ser 65 70 75 80gtt gcc agg ccc agg cca cca tgg atg ggt ctg ctg ggt cct acc atc 288Val Ala Arg Pro Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile 85 90 95cag gct gag gtt tac gac acg gtg gtc gtt acc ctg aag aac atg gct 336Gln Ala Glu Val Tyr Asp Thr Val Val Val Thr Leu Lys Asn Met Ala 100 105 110tct cat ccc gtt agt ctt cac gct gtc ggc gtc tcc ttc tgg aaa tct 384Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Phe Trp Lys Ser 115 120 125tcc gaa ggc gct gaa tat gag gat cac acc agc caa agg gag aag gaa 432Ser Glu Gly Ala Glu Tyr Glu Asp His Thr Ser Gln Arg Glu Lys Glu 130 135 140gac gat aaa gtc ctt ccc ggt aaa agc caa acc tac gtc tgg cag gtc 480Asp Asp Lys Val Leu Pro Gly Lys Ser Gln Thr Tyr Val Trp Gln Val145 150 155 160ctg aaa gaa aat ggt cca aca gcc tct gac cca cca tgt ctt acc tac 528Leu Lys Glu Asn Gly Pro Thr Ala Ser Asp Pro Pro Cys Leu Thr Tyr 165 170 175tca tac ctg tct cac gtg gac ctg gtg aaa gac ctg aat tcg ggc ctc 576Ser Tyr Leu Ser His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu 180 185 190att gga gcc ctg ctg gtt tgt aga gaa ggg agt ctg acc aga gaa agg 624Ile Gly Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Thr Arg Glu Arg 195 200 205acc cag aac ctg cac gaa ttt gta cta ctt ttt gct gtc ttt gat gaa 672Thr Gln Asn Leu His Glu Phe Val Leu Leu Phe Ala Val Phe Asp Glu 210 215 220ggg aaa agt tgg cac tca gca aga aat gac tcc tgg aca cgg gcc atg 720Gly Lys Ser Trp His Ser Ala Arg Asn Asp Ser Trp Thr Arg Ala Met225 230 235 240gat ccc gca cct gcc agg gcc cag cct gca atg cac aca gtc aat ggc 768Asp Pro Ala Pro Ala Arg Ala Gln Pro Ala Met His Thr Val Asn Gly 245 250 255tat gtc aac agg tct ctg cca ggt ctg atc gga tgt cat aag aaa tca 816Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His Lys Lys Ser 260 265 270gtc tac tgg cac gtg att gga atg ggc acc agc ccg gaa gtg cac tcc 864Val Tyr Trp His Val Ile Gly Met Gly Thr Ser Pro Glu Val His Ser 275 280 285att ttt ctt gaa ggc cac acg ttt ctc gtg agg cac cat cgc cag gct 912Ile Phe Leu Glu Gly His Thr Phe Leu Val Arg His His Arg Gln Ala 290 295 300tcc ttg gag atc tcg cca cta act ttc ctc act gct cag aca ttc ctg 960Ser Leu Glu Ile Ser Pro Leu Thr Phe Leu Thr Ala Gln Thr Phe Leu305 310 315 320atg gac ctt ggc cag ttc cta ctg ttt tgt cat atc tct tcc cac cac 1008Met Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser Ser His His 325 330 335cat ggt ggc atg gag gct cac gtc aga gta gaa agc tgc gcc gag gag 1056His Gly Gly Met Glu Ala His Val Arg Val Glu Ser Cys Ala Glu Glu 340 345 350ccc cag ctg cgg agg aaa gct gat gaa gag gaa gat tat gat gac aat 1104Pro Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu Asp Tyr Asp Asp Asn 355 360 365ttg tac gac tcg gac atg gac gtg gtc cgg ctc gat ggt gac gac gtg 1152Leu Tyr Asp Ser Asp Met Asp Val Val Arg Leu Asp Gly Asp Asp Val 370 375 380tct ccc ttt atc caa atc cgc tcg gtt gcc aag aag cat ccc aaa acc 1200Ser Pro Phe Ile Gln Ile Arg Ser Val Ala Lys Lys His Pro Lys Thr385 390 395 400tgg gtg cac tac atc tct gca gag gag gag gac tgg gac tac gcc ccc 1248Trp Val His Tyr Ile Ser Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro 405 410 415gcg gtc ccc agc ccc agt gac aga agt tat aaa agt ctc tac ttg aac 1296Ala Val Pro Ser Pro Ser Asp Arg Ser Tyr Lys Ser Leu Tyr Leu Asn 420 425 430agt ggt cct cag cga att ggt agg aaa tac aaa aaa gct cga ttc gtc 1344Ser Gly Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys Ala Arg Phe Val 435 440 445gct tac acg gat gta aca ttt aag act cgt aaa gct att ccg tat gaa 1392Ala Tyr Thr Asp Val Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr Glu 450 455 460tca gga atc ctg gga cct tta ctt tat gga gaa gtt gga gac aca ctt 1440Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu465 470 475 480ttg att ata ttt aag aat aaa gcg agc cga cca tat aac atc tac cct 1488Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro Tyr Asn Ile Tyr Pro 485 490 495cat gga atc act gat gtc agc gct ttg cac cca ggg aga ctt cta aaa 1536His Gly Ile Thr Asp Val Ser Ala Leu His Pro Gly Arg Leu Leu Lys 500 505 510ggt tgg aaa cat ttg aaa gac atg cca att ctg cca gga gag act ttc 1584Gly Trp Lys His Leu Lys Asp Met Pro Ile Leu Pro Gly Glu Thr Phe 515 520 525aag tat aaa tgg aca gtg act gtg gaa gat ggg cca acc aag tcc gat 1632Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp 530 535 540cct cgg tgc ctg acc cgc tac tac tcg agc tcc att aat cta gag aaa 1680Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Ser Ile Asn Leu Glu Lys545 550 555 560gat ctg gct tcg gga ctc att ggc cct ctc ctc atc tgc tac aaa gaa 1728Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu 565 570 575tct gta gac caa aga gga aac cag atg atg tca gac aag aga aac gtc 1776Ser Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn Val 580 585 590atc ctg ttt tct gta ttc gat gag aat caa agc tgg tac ctc gca gag 1824Ile Leu Phe Ser Val Phe Asp Glu Asn Gln Ser Trp Tyr Leu Ala Glu 595 600 605aat att cag cgc ttc ctc ccc aat ccg gat gga tta cag ccc cag gat 1872Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp Gly Leu Gln Pro Gln Asp 610 615 620cca gag ttc caa gct tct aac atc atg cac agc atc aat ggc tat gtt 1920Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val625 630 635 640ttt gat agc ttg cag ctg tcg gtt tgt ttg cac gag gtg gca tac tgg 1968Phe Asp Ser Leu Gln Leu Ser Val Cys Leu His Glu Val Ala Tyr Trp 645 650 655tac att cta agt gtt gga gca cag acg gac ttc ctc tcc gtc ttc ttc 2016Tyr Ile Leu Ser Val Gly Ala Gln Thr Asp Phe Leu Ser Val Phe Phe 660 665 670tct ggc tac acc ttc aaa cac aaa atg gtc tat gaa gac aca ctc acc 2064Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr 675 680 685ctg ttc ccc ttc tca gga gaa acg gtc ttc atg tca atg gaa aac cca 2112Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro 690 695 700ggt ctc tgg gtc ctt ggg tgc cac aac tca gac ttg cgg aac aga ggg 2160Gly Leu Trp Val Leu Gly Cys His Asn Ser Asp Leu Arg Asn Arg Gly705 710 715 720atg aca gcc tta ctg aag gtg tat agt tgt gac agg gac att ggt gat 2208Met Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp Arg Asp Ile Gly Asp 725 730 735tat tat gac aac act tat gaa gat att cca ggc ttc ttg ctg agt gga 2256Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile Pro Gly Phe Leu Leu Ser Gly 740 745 750aag aat gtc att gaa cct agg agc ttt gcc cag aat tca aga ccc cct 2304Lys Asn Val Ile Glu Pro Arg Ser Phe Ala Gln Asn Ser Arg Pro Pro 755 760 765agt gcg agc gct cca aag cct ccg gtc ctg cga cgg cat cag agg gac 2352Ser Ala Ser Ala Pro Lys Pro Pro Val Leu Arg Arg His Gln Arg Asp 770 775 780ata agc ctt cct act ttt cag ccg gag gaa gac aaa atg gac tat gat 2400Ile Ser Leu Pro Thr Phe Gln Pro Glu Glu Asp Lys Met Asp Tyr Asp785 790 795 800gat atc ttc tca act gaa acg aag gga gaa gat ttt gac att tac ggt 2448Asp Ile Phe Ser Thr Glu Thr Lys Gly Glu Asp Phe Asp Ile Tyr Gly 805 810 815gag gat gaa aat cag gac cct cgc agc ttt cag aag aga acc cga cac 2496Glu Asp Glu Asn Gln Asp Pro Arg Ser Phe Gln Lys Arg Thr Arg His 820 825 830tat ttc att gct gcg gtg gag cag ctc tgg gat tac ggg atg agc gaa 2544Tyr Phe Ile Ala Ala Val Glu Gln Leu Trp Asp Tyr Gly Met Ser Glu 835 840 845tcc ccc cgg gcg cta aga aac agg gct cag aac gga gag gtg cct cgg 2592Ser Pro Arg Ala Leu Arg Asn Arg Ala Gln Asn Gly Glu Val Pro Arg 850 855 860ttc aag aag gtg gtc ttc cgg gaa ttt gct gac ggc tcc ttc acg cag 2640Phe Lys Lys Val Val Phe Arg Glu Phe Ala Asp Gly Ser Phe Thr Gln865 870 875 880ccg tcg tac cgc ggg gaa ctc aac aaa cac ttg ggg ctc ttg gga ccc 2688Pro Ser Tyr Arg Gly Glu Leu Asn Lys His Leu Gly Leu Leu Gly Pro 885 890 895tac atc aga gcg gaa gtt gaa gac aac atc atg gta act ttc aaa aac 2736Tyr Ile Arg Ala Glu Val Glu Asp Asn Ile Met Val Thr Phe Lys Asn 900 905 910cag gcg tct cgt ccc tat tcc ttc tac tcg agc ctt att tct tat ccg 2784Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser Ser Leu Ile Ser Tyr Pro 915 920 925gat gat cag gag caa ggg gca gaa cct cga cac aac ttc gtc cag cca 2832Asp Asp Gln Glu Gln Gly Ala Glu Pro Arg His Asn Phe Val Gln Pro 930 935 940aat gaa acc aga act tac ttt tgg aaa gtg cag cat cac atg gca ccc 2880Asn Glu Thr Arg Thr Tyr Phe Trp Lys Val Gln His His Met Ala Pro945 950 955 960aca gaa gac gag ttt gac tgc aaa gcc tgg gcc tac ttt tct gat gtt 2928Thr Glu Asp Glu Phe Asp Cys Lys Ala Trp Ala Tyr Phe Ser Asp Val 965 970 975gac ctg gaa aaa gat gtg cac tca ggc ttg atc ggc ccc ctt ctg atc 2976Asp Leu Glu Lys Asp Val His Ser Gly Leu Ile Gly Pro Leu Leu Ile 980 985 990tgc cgc gcc aac acc ctg aac gct gct cac ggt aga caa gtg acc gtg 3024Cys Arg Ala Asn Thr Leu Asn Ala Ala His Gly Arg Gln Val Thr Val 995 1000 1005caa gaa ttt gct ctg ttt ttc act att ttt gat gag aca aag agc tgg 3072Gln Glu Phe Ala Leu Phe Phe Thr Ile Phe Asp Glu Thr Lys Ser Trp 1010 1015 1020tac ttc act gaa aat gtg gaa agg aac tgc cgg gcc ccc tgc cat ctg 3120Tyr Phe Thr Glu Asn Val Glu Arg Asn Cys Arg Ala Pro Cys His Leu1025 1030 1035 1040cag atg gag gac ccc act ctg aaa gaa aac tat cgc ttc cat gca atc 3168Gln Met Glu Asp Pro Thr Leu Lys Glu Asn Tyr Arg Phe His Ala Ile 1045 1050 1055aat ggc tat gtg atg gat aca ctc cct ggc tta gta atg gct cag aat 3216Asn Gly Tyr Val Met Asp Thr Leu Pro Gly Leu Val Met Ala Gln Asn 1060 1065 1070caa agg atc cga tgg tat ctg ctc agc atg ggc agc aat gaa aat atc 3264Gln Arg Ile Arg Trp Tyr Leu Leu Ser Met Gly Ser Asn Glu Asn Ile 1075 1080 1085cat tcg att cat ttt agc gga cac gtg ttc agt gta cgg aaa aag gag 3312His Ser Ile His Phe Ser Gly His Val Phe Ser Val Arg Lys Lys Glu 1090 1095 1100gag tat aaa atg gcc gtg tac aat ctc tat ccg ggt gtc ttt gag aca 3360Glu Tyr Lys Met Ala Val Tyr Asn Leu Tyr Pro Gly Val Phe Glu Thr1105 1110 1115 1120gtg gaa atg cta ccg tcc aaa gtt gga att tgg cga ata gaa tgc ctg 3408Val Glu Met Leu Pro Ser Lys Val Gly Ile Trp Arg Ile Glu Cys Leu 1125 1130 1135att ggc gag cac ctg caa gct ggg atg agc acg act ttc ctg gtg tac 3456Ile Gly Glu His Leu Gln Ala Gly Met Ser Thr Thr Phe Leu Val Tyr 1140 1145 1150agc aag gag tgt cag gct cca ctg gga atg gct tct gga cgc att aga 3504Ser Lys Glu Cys Gln Ala Pro Leu Gly Met Ala Ser Gly Arg Ile Arg 1155 1160 1165gat ttt cag atc aca gct tca gga cag tat gga cag tgg gcc cca aag 3552Asp Phe Gln Ile Thr Ala Ser Gly Gln Tyr Gly Gln Trp Ala Pro Lys 1170 1175 1180ctg gcc aga ctt cat tat tcc gga tca atc aat gcc tgg agc acc aag 3600Leu Ala Arg Leu His Tyr Ser Gly Ser Ile Asn Ala Trp Ser Thr Lys1185 1190 1195 1200gat ccc cac tcc tgg atc aag gtg gat ctg ttg gca cca atg atc att 3648Asp Pro His Ser Trp Ile Lys Val Asp Leu Leu Ala Pro Met Ile Ile 1205 1210 1215cac ggc atc atg acc cag ggt gcc cgt cag aag ttt tcc agc ctc tac 3696His Gly Ile Met Thr Gln Gly Ala Arg Gln Lys Phe Ser Ser Leu Tyr 1220 1225 1230atc tcc cag ttt atc atc atg tac agt ctt gac ggg agg aac tgg cag 3744Ile Ser Gln Phe Ile Ile Met Tyr Ser Leu Asp Gly Arg Asn Trp Gln 1235 1240 1245agt tac cga ggg aat tcc acg ggc acc tta atg gtc ttc ttt ggc aat 3792Ser Tyr Arg Gly Asn Ser Thr Gly Thr Leu Met Val Phe Phe Gly Asn 1250 1255 1260gtg gac gca tct ggg att aaa cac aat att ttt aac cct ccg att gtg 3840Val Asp Ala Ser Gly Ile Lys His Asn Ile Phe Asn Pro Pro Ile Val1265 1270 1275 1280gct cgg tac atc cgt ttg cac cca aca cat tac agc atc cgc agc act 3888Ala Arg Tyr Ile Arg Leu His Pro Thr His Tyr Ser Ile Arg Ser Thr 1285 1290 1295ctt cgc atg gag ttg atg ggc tgt gat tta aac agt tgc agc atg ccc 3936Leu Arg Met Glu Leu Met Gly Cys Asp Leu Asn Ser Cys Ser Met Pro 1300 1305 1310ctg gga atg cag aat aaa gcg ata tca gac tca cag atc acg gcc tcc 3984Leu Gly Met Gln Asn Lys Ala Ile Ser Asp Ser Gln Ile Thr Ala Ser 1315 1320 1325tcc cac cta agc aat ata ttt gcc acc tgg tct cct tca caa gcc cga 4032Ser His Leu Ser Asn Ile Phe Ala Thr Trp Ser Pro Ser Gln Ala Arg 1330 1335 1340ctt cac ctc cag ggg cgg acg aat gcc tgg cga ccc cgg gtg agc agc 4080Leu His Leu Gln Gly Arg Thr Asn Ala Trp Arg Pro Arg Val Ser Ser1345 1350 1355 1360gca gag gag tgg ctg cag gtg gac ctg cag aag acg gtg aag gtc aca 4128Ala Glu Glu Trp Leu Gln Val Asp Leu Gln Lys Thr Val Lys Val Thr 1365 1370 1375ggc atc acc acc cag ggc gtg aag tcc ctg ctc agc agc atg tat gtg 4176Gly Ile Thr Thr Gln Gly Val Lys Ser Leu Leu Ser Ser Met Tyr Val 1380 1385 1390aag gag ttc ctc gtg tcc agt agt cag gac ggc cgc cgc tgg acc ctg 4224Lys Glu Phe Leu Val Ser Ser Ser Gln Asp Gly Arg Arg Trp Thr Leu 1395 1400 1405ttt ctt cag gac ggc cac acg aag gtt ttt cag ggc aat cag gac tcc 4272Phe Leu Gln Asp Gly His Thr Lys Val Phe Gln Gly Asn Gln Asp Ser 1410 1415 1420tcc acc ccc gtg gtg aac gct ctg gac ccc ccg ctg ttc acg cgc tac 4320Ser Thr Pro Val Val Asn Ala Leu Asp Pro Pro Leu Phe Thr Arg Tyr1425 1430 1435 1440ctg agg atc cac ccc acg agc tgg gcg cag cac atc gcc ctg agg ctc 4368Leu Arg Ile His Pro Thr Ser Trp Ala Gln His Ile Ala Leu Arg Leu 1445 1450 1455gag gtt cta gga tgt gag gca cag gat ctc tac tga 4404Glu Val Leu Gly Cys Glu Ala Gln Asp Leu Tyr 1460 1465 38 1467 PRT Porcine 38Met Gln Leu Glu Leu Ser Thr Cys Val Phe Leu Cys Leu Leu Pro Leu 1 5 10 15Gly Phe Ser Ala Ile Arg Arg Tyr Tyr Leu Gly Ala Val Glu Leu Ser 20 25 30Trp Asp Tyr Arg Gln Ser Glu Leu Leu Arg Glu Leu His Val Asp Thr 35 40 45Arg Phe Pro Ala Thr Ala Pro Gly Ala Leu Pro Leu Gly Pro Ser Val 50 55 60Leu Tyr Lys Lys Thr Val Phe Val Glu Phe Thr Asp Gln Leu Phe Ser 65 70 75 80Val Ala Arg Pro Arg Pro Pro Trp Met Gly Leu Leu Gly Pro Thr Ile 85 90 95Gln Ala Glu Val Tyr Asp Thr Val Val Val Thr Leu Lys Asn Met Ala 100 105 110Ser His Pro Val Ser Leu His Ala Val Gly Val Ser Phe Trp Lys Ser 115 120 125Ser Glu Gly Ala Glu Tyr Glu Asp His Thr Ser Gln Arg Glu Lys Glu 130 135 140Asp Asp Lys Val Leu Pro Gly Lys Ser Gln Thr Tyr Val Trp Gln Val145 150 155 160Leu Lys Glu Asn Gly Pro Thr Ala Ser Asp Pro Pro Cys Leu Thr Tyr 165 170 175Ser Tyr Leu Ser His Val Asp Leu Val Lys Asp Leu Asn Ser Gly Leu 180 185 190Ile Gly Ala Leu Leu Val Cys Arg Glu Gly Ser Leu Thr Arg Glu Arg 195 200 205Thr Gln Asn Leu His Glu Phe Val Leu Leu Phe Ala Val Phe Asp Glu 210 215 220Gly Lys Ser Trp His Ser Ala Arg Asn Asp Ser Trp Thr Arg Ala Met225 230 235 240Asp Pro Ala Pro Ala Arg Ala Gln Pro Ala Met His Thr Val Asn Gly 245 250 255Tyr Val Asn Arg Ser Leu Pro Gly Leu Ile Gly Cys His Lys Lys Ser 260 265 270Val Tyr Trp His Val Ile Gly Met Gly Thr Ser Pro Glu Val His Ser 275 280 285Ile Phe Leu Glu Gly His Thr Phe Leu Val Arg His His Arg Gln Ala 290 295 300Ser Leu Glu Ile Ser Pro Leu Thr Phe Leu Thr Ala Gln Thr Phe Leu305 310 315 320Met Asp Leu Gly Gln Phe Leu Leu Phe Cys His Ile Ser Ser His His 325 330 335His Gly Gly Met Glu Ala His Val Arg Val Glu Ser Cys Ala Glu Glu 340 345 350Pro Gln Leu Arg Arg Lys Ala Asp Glu Glu Glu Asp Tyr Asp Asp Asn 355 360 365Leu Tyr Asp Ser Asp Met Asp Val Val Arg Leu Asp Gly Asp Asp Val 370 375 380Ser Pro Phe Ile Gln Ile Arg Ser Val Ala Lys Lys His Pro Lys Thr385 390 395 400Trp Val His Tyr Ile Ser Ala Glu Glu Glu Asp Trp Asp Tyr Ala Pro 405 410 415Ala Val Pro Ser Pro Ser Asp Arg Ser Tyr Lys Ser Leu Tyr Leu Asn 420 425 430Ser Gly Pro Gln Arg Ile Gly Arg Lys Tyr Lys Lys Ala Arg Phe Val 435 440 445Ala Tyr Thr Asp Val Thr Phe Lys Thr Arg Lys Ala Ile Pro Tyr Glu 450 455 460Ser Gly Ile Leu Gly Pro Leu Leu Tyr Gly Glu Val Gly Asp Thr Leu465 470 475 480Leu Ile Ile Phe Lys Asn Lys Ala Ser Arg Pro Tyr Asn Ile Tyr Pro 485 490 495His Gly Ile Thr Asp Val Ser Ala Leu His Pro Gly Arg Leu Leu Lys 500 505 510Gly Trp Lys His Leu Lys Asp Met Pro Ile Leu Pro Gly Glu Thr Phe 515 520 525Lys Tyr Lys Trp Thr Val Thr Val Glu Asp Gly Pro Thr Lys Ser Asp 530 535 540Pro Arg Cys Leu Thr Arg Tyr Tyr Ser Ser Ser Ile Asn Leu Glu Lys545 550 555 560Asp Leu Ala Ser Gly Leu Ile Gly Pro Leu Leu Ile Cys Tyr Lys Glu 565 570 575Ser Val Asp Gln Arg Gly Asn Gln Met Met Ser Asp Lys Arg Asn Val 580 585 590Ile Leu Phe Ser Val Phe Asp Glu Asn Gln Ser Trp Tyr Leu Ala Glu 595 600 605Asn Ile Gln Arg Phe Leu Pro Asn Pro Asp Gly Leu Gln Pro Gln Asp 610 615 620Pro Glu Phe Gln Ala Ser Asn Ile Met His Ser Ile Asn Gly Tyr Val625 630 635 640Phe Asp Ser Leu Gln Leu Ser Val Cys Leu His Glu Val Ala Tyr Trp 645 650 655Tyr Ile Leu Ser Val Gly Ala Gln Thr Asp Phe Leu Ser Val Phe Phe 660 665 670Ser Gly Tyr Thr Phe Lys His Lys Met Val Tyr Glu Asp Thr Leu Thr 675 680 685Leu Phe Pro Phe Ser Gly Glu Thr Val Phe Met Ser Met Glu Asn Pro 690 695 700Gly Leu Trp Val Leu Gly Cys His Asn Ser Asp Leu Arg Asn Arg Gly705 710 715 720Met Thr Ala Leu Leu Lys Val Tyr Ser Cys Asp Arg Asp Ile Gly Asp 725 730 735Tyr Tyr Asp Asn Thr Tyr Glu Asp Ile Pro Gly Phe Leu Leu Ser Gly 740 745 750Lys Asn Val Ile Glu Pro Arg Ser Phe Ala Gln Asn Ser Arg Pro Pro 755 760 765Ser Ala Ser Ala Pro Lys Pro Pro Val Leu Arg Arg His Gln Arg Asp 770 775 780Ile Ser Leu Pro Thr Phe Gln Pro Glu Glu Asp Lys Met Asp Tyr Asp785 790 795 800Asp Ile Phe Ser Thr Glu Thr Lys Gly Glu Asp Phe Asp Ile Tyr Gly 805 810 815Glu Asp Glu Asn Gln Asp Pro Arg Ser Phe Gln Lys Arg Thr Arg His 820 825 830Tyr Phe Ile Ala Ala Val Glu Gln Leu Trp Asp Tyr Gly Met Ser Glu 835 840 845Ser Pro Arg Ala Leu Arg Asn Arg Ala Gln Asn Gly Glu Val Pro Arg 850 855 860Phe Lys Lys Val Val Phe Arg Glu Phe Ala Asp Gly Ser Phe Thr Gln865 870 875 880Pro Ser Tyr Arg Gly Glu Leu Asn Lys His Leu Gly Leu Leu Gly Pro 885 890 895Tyr Ile Arg Ala Glu Val Glu Asp Asn Ile Met Val Thr Phe Lys Asn 900 905 910Gln Ala Ser Arg Pro Tyr Ser Phe Tyr Ser Ser Leu Ile Ser Tyr Pro 915 920 925Asp Asp Gln Glu Gln Gly Ala Glu Pro Arg His Asn Phe Val Gln Pro 930 935 940Asn Glu Thr Arg Thr Tyr Phe Trp Lys Val Gln His His Met Ala Pro945 950 955 960Thr Glu Asp Glu Phe Asp Cys Lys Ala Trp Ala Tyr Phe Ser Asp Val 965 970 975Asp Leu Glu Lys Asp Val His Ser Gly Leu Ile Gly Pro Leu Leu Ile 980 985 990Cys Arg Ala Asn Thr Leu Asn Ala Ala His Gly Arg Gln Val Thr Val 995 1000 1005Gln Glu Phe Ala Leu Phe Phe Thr Ile Phe Asp Glu Thr Lys Ser Trp 1010 1015 1020Tyr Phe Thr Glu Asn Val Glu Arg Asn Cys Arg Ala Pro Cys His Leu1025 1030 1035 1040Gln Met Glu Asp Pro Thr Leu Lys Glu Asn Tyr Arg Phe His Ala Ile 1045 1050 1055Asn Gly Tyr Val Met Asp Thr Leu Pro Gly Leu Val Met Ala Gln Asn 1060 1065 1070Gln Arg Ile Arg Trp Tyr Leu Leu Ser Met Gly Ser Asn Glu Asn Ile 1075 1080 1085His Ser Ile His Phe Ser Gly His Val Phe Ser Val Arg Lys Lys Glu 1090 1095 1100Glu Tyr Lys Met Ala Val Tyr Asn Leu Tyr Pro Gly Val Phe Glu Thr1105 1110 1115 1120Val Glu Met Leu Pro Ser Lys Val Gly Ile Trp Arg Ile Glu Cys Leu 1125 1130 1135Ile Gly Glu His Leu Gln Ala Gly Met Ser Thr Thr Phe Leu Val Tyr 1140 1145 1150Ser Lys Glu Cys Gln Ala Pro Leu Gly Met Ala Ser Gly Arg Ile Arg 1155 1160 1165Asp Phe Gln Ile Thr Ala Ser Gly Gln Tyr Gly Gln Trp Ala Pro Lys 1170 1175 1180Leu Ala Arg Leu His Tyr Ser Gly Ser Ile Asn Ala Trp Ser Thr Lys1185 1190 1195 1200Asp Pro His Ser Trp Ile Lys Val Asp Leu Leu Ala Pro Met Ile Ile 1205 1210 1215His Gly Ile Met Thr Gln Gly Ala Arg Gln Lys Phe Ser Ser Leu Tyr 1220 1225 1230Ile Ser Gln Phe Ile Ile Met Tyr Ser Leu Asp Gly Arg Asn Trp Gln 1235 1240 1245Ser Tyr Arg Gly Asn Ser Thr Gly Thr Leu Met Val Phe Phe Gly Asn 1250 1255 1260Val Asp Ala Ser Gly Ile Lys His Asn Ile Phe Asn Pro Pro Ile Val1265 1270 1275 1280Ala Arg Tyr Ile Arg Leu His Pro Thr His Tyr Ser Ile Arg Ser Thr 1285 1290 1295Leu Arg Met Glu Leu Met Gly Cys Asp Leu Asn Ser Cys Ser Met Pro 1300 1305 1310Leu Gly Met Gln Asn Lys Ala Ile Ser Asp Ser Gln Ile Thr Ala Ser 1315 1320 1325Ser His Leu Ser Asn Ile Phe Ala Thr Trp Ser Pro Ser Gln Ala Arg 1330 1335 1340Leu His Leu Gln Gly Arg Thr Asn Ala Trp Arg Pro Arg Val Ser Ser1345 1350 1355 1360Ala Glu Glu Trp Leu Gln Val Asp Leu Gln Lys Thr Val Lys Val Thr 1365 1370 1375Gly Ile Thr Thr Gln Gly Val Lys Ser Leu Leu Ser Ser Met Tyr Val 1380 1385 1390Lys Glu Phe Leu Val Ser Ser Ser Gln Asp Gly Arg Arg Trp Thr Leu 1395 1400 1405Phe Leu Gln Asp Gly His Thr Lys Val Phe Gln Gly Asn Gln Asp Ser 1410 1415 1420Ser Thr Pro Val Val Asn Ala Leu Asp Pro Pro Leu Phe Thr Arg Tyr1425 1430 1435 1440Leu Arg Ile His Pro Thr Ser Trp Ala Gln His Ile Ala Leu Arg Leu 1445 1450 1455Glu Val Leu Gly Cys Glu Ala Gln Asp Leu Tyr 1460 1465

Claims

1. An isolated DNA molecule encoding the amino acid sequence of POL1212 as set forth in SEQ ID NO:38.

2. An expression vector comprising a DNA molecule according to claim 1.

3. An isolated DNA molecule according to claim 1 having the nucleotide sequence of SEQ ID NO:37.

4. An expression vector comprising a DNA molecule according to claim 3.

5. An isolated mammalian host cell containing and replicating an expression vector comprising DNA encoding the amino acid sequence of POL1212 as set forth in SEQ ID NO:38.

6. An isolated mammalian host cell according to claim 5 wherein the vector comprises DNA having the nucleotide sequence of SEQ ID NO:37.

7. A cell according to claim 6 wherein the host cell is BHK CRL-1632.

8. A method for producing a modified porcine factor VIII protein having the amino acid sequence of SEQ ID NO:38 comprising expressing in a mammalian host cell a DNA molecule encoding the amino acid sequence of SEQ ID NO:38.

9. The method of claim 8 wherein the DNA molecule encoding the amino acid sequence of SEQ ID NO:38 also encodes a signal peptide, whereby the modified porcine factor VIII protein is from the most cell.

10. The method of claim 9 wherein the signal peptide has the sequence of amino acids 1-19 of SEQ ID NO:30.