Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid
Reexamination Certificate
1998-12-11
2001-03-06
Patterson, Jr., Charles L. (Department: 1652)
Chemistry: molecular biology and microbiology
Measuring or testing process involving enzymes or...
Involving nucleic acid
C435S226000, C424S094640, C530S387900, C536S023200
Reexamination Certificate
active
06197511
ABSTRACT:
FIELD OF THE INVENTION
This invention relates to nucleic acid and amino acid sequences of a novel human allikrein and to the use of these sequences in the diagnosis, prevention, and treatment of cancer and skin disorders.
BACKGROUND OF THE INVENTION
Stratum corneum chymotryptic enzyme (SCCE) is a member of the kallikrein family of serine proteases. Hansson L. et al. (1994; J. Biol. Chem. 269: 19420-19426) cloned the SCCE gene and showed that it is expressed specifically in the outermost layer of the epidermis, known as the stratum corneum. SCCE is likely to function in proteolysis of intercellular cohesive structures. Such proteolysis is necessary for desquamation, the ongoing process by which outer layers of skin are eliminated. An imbalance in desquamation and new epidermis growth may lead to the formation of scales on the skin surface, a common occurence in diseases such as psoriasis and icthyosis.
Genes encoding the three human kallikreins, tissue kallikrein (KLK1), glandular kallikrein (KLK2), and PSA are located in a cluster at chromosome map position 19q 13.2-q 13.4 (Riegmen P. H. (1992) Genomics 14: 6-11). PSA shares more extensive homology with KLK2 than with KLK1. Both PSA and KLK2 are produced by prostate epithelial cells and their expression is regulated by androgens. Three amino acid residues were found to be critical for serine protease activity, residues H
65
, D
120
, and S
213
in PSA (Bridon D. P. et al. (1995) Urology 45: 801-806). Substrate specificity, described as chymotrypsinogen-like (with KLK2) or trypsin-like (with PSA) is thought to be determined by S
207
in PSA and D
209
in KLK2 (Bridon et al., supra). KLK1 is chymotrypsinogen-like and expressed in the pancreas, urinary system, and sublingual gland. KLK1, like the other kallikreins, is made as a pre-pro-protein and is processed into an active form of 238 amino acids by cleavage of a 24 amino acid terminal signal sequence (Fukushima D. et al. (1985) Biochemistry 24: 8037-8043).
Adenocarcinoma of the prostate accounts for a significant number of malignancies in men over 50, with over 122,000 new cases occurring per year, in the United States alone. Prostate-specific antigen (PSA) is the most sensitive marker available for monitoring cancer progression and response to therapy. Serum PSA is elevated in up to 92% of patients with prostatic carcinoma, depending upon tumor volume.
Discovery of proteins related to SCCE, PAS, and the polynucleotides encoding them satisfies a need in the art by providing new compositions useful in diagnosis, prevention, and treatment of cancer and skin disorders.
SUMMARY OF THE INVENTION
The present invention features a novel human kallikrein hereinafter designated HKALL and characterized as having chemical and structural similarity to human stratum corneum chymotryptic enzyme and other kallikreins.
Accordingly, the invention features a substantially purified HKALL which has the amino acid sequence shown in SEQ ID NO:1.
One aspect of the invention features isolated and substantially purified polynucleotides that encode HKALL. In a particular aspect, the polynucleotide is the nucleotide sequence of SEQ ID NO:2.
The invention also relates to a polynucleotide sequence comprising the complement of SEQ ID NO:2 or variants thereof. In addition, the invention features polynucleotide sequences which hybridize under stringent conditions to SEQ ID NO:2.
The invention additionally features nucleic acid sequences encoding polypeptides, oligonucleotides, peptide nucleic acids (PNA), fragments, portions or antisense molecules thereof, and expression vectors and host cells comprising polynucleotides that encode HKALL. The present invention also features antibodies which bind specifically to HKALL, and pharmaceutical compositions comprising substantially purified HKALL. The invention also features the use of agonists and antagonists of HKALL. The invention also features a method for producing HKALL using the host cell, and methods for treating cancer and skin disorders by administering an antagonist to HKALL.
REFERENCES:
patent: 95 /00651 (1995-01-01), None
Hansson, L. et al., “Cloning, Expression, and Charaterization of Stratum Corneum Chymotryptic Enzyme”,J. Biol. Chem., 269: 19420-19426 (1994) (GI 521214) (GI 532504).
Riegman, P.H.J. et al., “Characterization of the Human Kallikrein Locus”,Genomics, 14: 6-11 (1992) (GI 186652) (GI 186653).
Bridon, D.P. et al., “Structual Comparison Of Prostate-Specific Antigen And Human Glandular Kallikrein Using Molecular Modeling”,Urology, 45: 801-806.
Fukushima, D. et al., “Nucleotide Sequence of Cloned cDNA for Human Pancreatic Kallikrein”,Biochemistry27: 8037-8043 (1985).
Fahnestock, M. et al., “Characterization of Kallikrein cDNAs from the African Rodent Mastomys”,DNA and Cell Biology, 13: 293-300 (1994) (GI 55526) (GI 55527).
Hillier, L. et al. zd55e11.s1 Soares Fetal Heart NbHH19WHomo sapienscDNA Clone 344588 3′ Similar to PIR:A53968 Serine Protease SCCE Precursor—Human, EST-STS Accession No. W73140, Public Availibility Date Jun. 14, 1996.
EMBL/GenBank Databases Accession No. W73168, Sequence reference HS168367, Hillier, L. et al.: “The WashU-Merck EST Project”, Jun. 20, 1996.
EMBL/GenBank Databases Accession No. W68496, Sequence reference HS496365, Hillier, L. Et al.: “The WashU-Merck EST Project”, Jun. 16, 1996.
EMBL/GenBank Databases Accession No. AA862032, Sequence reference AA862032, Hillier, L. Et al.: “The WashU-Merck EST Project”, Mar. 15, 1998.
Hillman Jennifer L.
Lal Preeti
Incyte Genomics Inc.
Incyte Genomics, Inc.
Patterson Jr. Charles L.
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