Claims
- 1. An isolated nucleic acid molecule which encodes a WRN gene product, wherein said nucleic acid molecule is selected from the group consisting of:
- (a) an isolated nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 70, 72, 205, and 207;
- (b) an isolated nucleic acid molecule that specifically hybridizes to the complement of the nucleic acid molecule of (a) under hybridization conditions of 5X SSPE, 0.5% SDS at 65.degree. C.; and
- (c) an isolated nucleic acid molecule which, due to the degeneracy of the nucleic acid code, encodes a WRN gene product encoded by the nucleic acid molecules of (a) or (b).
- 2. An expression vector comprising a promoter operably linked to a nucleic acid molecule according to claim 1.
- 3. The expression vector according to claim 2, wherein said promoter is selected from the group consisting of CMV I-E promoter, SV40 early promoter, and MuLVLTR promoter.
- 4. The expression vector according to claim 2, wherein said promoter is a tissue-specific promoter.
- 5. A viral vector comprising the nucleic acid molecule of claim 1.
- 6. The viral vector according to claim 5, wherein said viral vector is selected from the group consisting of herpes simplex viral vector, adenoviral vector, adeno-associated viral vector, and retroviral vector.
- 7. An isolated recombinant host cell comprising a vector according to any one of claims 2 to 6.
- 8. The recombinant host cell according to claim 7, wherein said cell is selected from the group consisting of human cell, dog cell, monkey cell, rat cell, and mouse cell.
- 9. An isolated nucleic acid molecule which specifically hybridizes to a WRN gene under hybridization conditions of 5X SSPE, 0.5% SDS at 65.degree. C., wherein said WRN gene comprises a nucleic acid molecule according to claim 1.
- 10. A primer pair which specifically amplifies a nucleic acid molecule according to claim 1.
- 11. The primer pair of claim 10, wherein said primer pair is selected from the group consisting of (a) SEQ ID NOS: 9 and 10, (b) SEQ ID NOS: 11 and 12, (c) SEQ ID NOS: 22 and 16, (d) SEQ ID NOS: 23 and 2, (e) SEQ ID NOS: 21 and 10, (f) SEQ ID NOS: 85 and 12, (g) SEQ ID NOS: 88 and 82, (h) SEQ ID NOS: 89 and 80, (I) SEQ ID NOS: 164 and 165, (j) SEQ ID NOS: 22 and 166, and (k) SEQ ID NOS: 167 and 168.
- 12. An oligonucleotide primer consisting of any one of SEQ ID NOS: 1-57, or a portion thereof of at least 12 nucleotides in length.
- 13. An oligonucleotide primer consisting of any one of SEQ ID NOS: 169-203, or a portion thereof of at least 12 nucleotides in length.
- 14. The primer pair of claim 10, wherein said primer pair amplifies an exon of the WRN gene, wherein said exon is selected from the group consisting of exon 1, 2, 3, 4, 5, 6, 7, 8, 9, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, and 35.
- 15. An isolated nucleic acid molecule for detecting the presence of a Werner Syndrome mutation in a subject, wherein said nucleic acid molecule consists of a nucleotide sequence selected from the group consisting of SEQ ID NO: 59, SEQ ID NO: 61, SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, and SEQ ID NO: 69.
CROSS-REFERENCES TO RELATED APPLICATIONS
This application is a continuation-in-part of U.S. patent application Ser. No. 08/632,175, filed Apr. 12, 1996, now abandoned; which is a continuation-in-part of U.S. patent application Ser. No. 08/594,242, filed Jan. 30, 1996, now abandoned; which is a continuation-in-part of U.S. patent application Ser. No. 08/580,539, filed Dec. 29, 1995, now abandoned. This application also claims priority from U.S. patent application Ser. No. 60/009,409 filed Dec. 29, 1995 and U.S. patent application Ser. No. 60/010,835 filed Jan. 30, 1996.
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Continuation in Parts (3)
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Number |
Date |
Country |
Parent |
632175 |
Apr 1996 |
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Parent |
594242 |
Jan 1996 |
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Parent |
580539 |
Dec 1995 |
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