Genes encoding several poly(ADP-ribose) glycohydrolase (PARG) enzymes, the proteins and fragments thereof, and antibodies immunoreactive therewith
View Patent ↗The isolation and characterization of cDNAs encoding poly(ADP-ribose) glycohydrolase (PARG) enzymes and the amino acid sequences of PARGs from several species are described. PARG is involved in the cellular response to DNA damage and its proper function is associated with the body's response to neoplastic disorder inducing agents and oxidative stress. Expression vectors containing the cDNAs and cells transformed with the vectors are described. Probes and primers that hybridize with the cDNAs are described. Expression of the cDNA in E. coli results in an enzymatically active protein of about 111 kDa and an active fragment of about 59 kDa. Methods for inhibiting PARG expression or overexpressing PARG in a subject for therapeutic benefit are described. Exemplary of PARG inhibitors are anti-sense oligonucleotides. The invention has implications for treatment of neoplastic disorder, heart attack, stroke, and neurodegenerative diseases. Methods for detecting a mutant PARG allele are also described. Antibodies immunoreactive with PARGs and fragments thereof are described.
1. An isolated antibody which binds specifically to a protein, which is a poly(ADP-ribose) glycohydrolase which catalyzes release of ADP-ribose from an ADP ribose polymer, encoded by a nucleotide sequence that is at least 80% identical to the nucleotide sequence set forth in SEQ ID NO: 1, wherein the protein has a molecular weight greater than 100 kilodaltons as determined by SDS PAGE.
2. The isolated antibody of claim 1 , wherein said isolated protein has the amino acid sequence set forth in SEQ ID NO: 2, 4, or 6.
3. The isolated antibody of claim 1 , encoded by a nucleotide sequence set forth in SEQ ID NO: 1, 3, or 5.
4. An isolated antibody which binds specifically to a protein, which is a poly(ADP-ribose) glycohydrolase which catalyzes release of ADP-ribose from an ADP-ribose polymer, wherein said protein comprises the amino acid sequence set forth in SEQ ID NO: 11, 12, 13 or 14, and has a molecular weight greater than 100 kilodaltons, as determined by SDS-PAGE.
5. The isolated antibody of claim 4 , which binds specifically to a protein encoded by a nucleic acid molecule, the complementary sequence of which hybridizes to the nucleotide sequence set forth in SEQ ID NO: 1 under the following conditions: prehybridization at 42° C. in 50% formamide, 0.25 M sodium phosphate buffer, pH 7.2, 0.25 M NaCl, 7% SDS, 1 mM EDTA for 10 hours, 100 ug denatured salmon sperm DNA, hybridization at 42° C. in 50% formamide, 0.25 M sodium phosphate buffer, 100 ug denatured salmon sperm DNA, pH 7.2, 0.25 M NaCl, 7% SDS, 1 mM EDTA.
6. An isolated antibody which binds specifically to a protein, which is a poly(ADP-ribose) glycohydrolase which catalyzes release of ADP-ribose from an ADP-ribose polymer, wherein said protein comprises amino acids 677-977 of SEQ ID NO: 4.
7. The isolated antibody of claim 1 , selected from the group consisting of an antibody and an antibody fragment.
8. The isolated antibody of claim 7 , wherein said antibody fragment is an Fc fragment, an Fab fragment, an Fab′ fragment, and an Fab′ (2) fragment.
9. The isolated antibody of claim 1 , wherein said antibody binds to the C terminus of said protein.
10. The isolated antibody of claim 1 , wherein said antibody binds to the N terminus of said protein.
11. The isolated antibody of claim 4 , selected from the group consisting of an antibody and an antibody fragment.
12. The isolated antibody of claim 1 , wherein said antibody fragment is an Fc fragment, an Fab fragment, an Fab′ fragment, and an Fab′ (2) fragment.
13. The isolated antibody of claim 4 , wherein said antibody binds to the C terminus of said protein.
14. The isolated antibody of claim 4 , wherein said antibody binds to the N terminus of said protein.