IP Library Granted Patent US 7,790,448
Granted Patent B2
US 7,790,448 · App. 11/898,468 · Granted Sep 7, 2010

Nucleic acid and gene derived from novel HCV strain and replicon-replicating cell using said gene

Assignees: Tokyo Metropolitan Organization for Medical Research; Toray Industries, Inc.
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Quick Facts
Patent No.
US 7,790,448
App. No.
11/898,468
Granted
Sep 7, 2010
Kind
B2
Abstract

The present invention relates to a gene derived from a novel fulminant hepatitis C virus strain, an HCV replicon RNA with a high replication efficiency obtained using the gene, and an HCV replicon-replicating cell transfected with the replicon RNA. When the HCV replicon RNA and the HCV replicon-replicating cell of the present invention are used, HCV proteins can be continuously produced in a large amount.

Claims (14)

1. An isolated nucleic acid comprising the nucleotide sequences shown by SEQ ID NO:2, SEQ ID NO:5, and SEQ ID NO:6;

provided that, if the nucleic acid is a DNA, the nucleotide symbol “u” in the sequence listings shall be replaced with “t”.

2. An isolated nucleic acid comprising the nucleotide sequence represented by SEQ ID NO:2;

provided that, if the nucleic acid is a DNA, the nucleotide symbol “u” in the sequence listing shall be replaced with “t”.

3. An isolated nucleic acid comprising the nucleotide sequence represented by SEQ ID NO:6;

provided that, if the nucleic acid is a DNA, the nucleotide symbol “u” in the sequence listing shall be replaced with “t”.

4. A replicon RNA comprising an RNA comprising the nucleotide sequences shown by SEQ ID NO:2, SEQ ID NO:5, and SEQ ID NO:6, wherein SEQ ID NO: 5 is located at the most 5′ end and 5′ in relation to SEQ ID NO: 2 and SEQ ID NO: 6 is located at the most 3′ end and 3′ in relation to SEQ ID NO:2.

5. The replicon RNA according to claim 4 , further comprising an IRES sequence.

6. The replicon RNA according to claim 5 , further comprising a selection marker gene or a reporter gene.

7. A replicon-replicating cell created by introducing the replicon RNA according to claim 4 into isolated cells.

8. The replicon-replicating cell according to claim 7 , wherein the isolated cells are human liver-derived cells, human cervix-derived cells, or human embryonic kidney-derived cells.

9. A method for screening for the ability of a substance to stimulate or suppress replication of hepatitis C virus, comprising culturing the replicon-replicating cell according to claim 7 in the presence of a test substance and detecting replication of a replicon RNA in the resulting culture.

10. A replicon-replicating cell created by introducing the replicon RNA according to claim 5 into isolated cells.

11. A replicon-replicating cell created by introducing the replicon RNA according to claim 6 into isolated cells.

Assignments (2)
CHANGE OF NAME Recorded Sep 20, 2011
From: TOKYO METROPOLITAN ORGANIZATION FOR MEDICAL RESEARCH
To: TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE
Reel/Frame 026931/0980 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2008
From: WAKITA, TAKAJI; KATO, TAKANOBU; DATE, TOMOKO; MIYAMOTO, MICHIKO
To: TOKYO METROPOLITAN ORGANIZATION FOR MEDICAL RESEARCH; TORAY INDUSTRIES, INC.
Reel/Frame 020680/0504 →
Priority Claims (1)
JP 2003-329082 · Sep 19, 2003 · national
Continuity (2)
Continuation In Part 1057247600
Related Publication 20090042181A1 · Feb 12, 2009