IP Library Granted Patent US 7,812,146
Granted Patent B2
US 7,812,146 · App. 10/944,277 · Granted Oct 12, 2010

Hybrid hepatocyte growth factor gene having high expression efficiency of two heterotypes of hepatocyte growth factor

Assignee: ViroMed Co., Ltd.
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Quick Facts
Patent No.
US 7,812,146
App. No.
10/944,277
Granted
Oct 12, 2010
Kind
B2
Abstract

The present invention relates to a hybrid Hepatocyte Growth Factor (HGF) gene which is prepared by inserting an inherent or foreign intron between exons 4 and 5 in HGF cDNA, which has a base sequence of SEQ ID NO: 2. The gene has high expression efficiency and simultaneously expresses two heterotypes of HGF and dHGF (deleted variant HGF). Further the gene may be used for treating or preventing ischemic or liver diseases.

Claims (52)

1. A hybrid Hepatocyte Growth Factor (HGF) construct comprising:

(a) a first cDNA which has the same sequence as exons 1-4 of the human HGF gene wherein said exons 1-4 are arranged in sequential order without an intron therebetween, or degenerates thereof which do not alter the amino acid sequence encoded by said first cDNA,

(b) a polynucleotide that has the same sequence as intron 4 of a HGF gene or a functional fragment thereof, and

(c) a second cDNA which has the same sequence as exons 5-18 of the human HGF gene wherein said exons 5-18 are arranged in sequential order without an intron therebetween, or degenerates thereof which do not alter the amino acid sequence encoded by said second cDNA;

wherein (b) is located between (a) and (c); and the HGF construct simultaneously encodes two heterotypes of human HGF.

2. The hybrid HGF construct of claim 1 , wherein the polynucleotide of (b) has the same sequence as the full intron 4 of the human HGF gene.

3. The hybrid HGF construct of claim 2 , wherein said hybrid HGF construct comprises SEQ ID NO:2.

4. The hybrid HGF construct of claim 1 , wherein polynucleotide of (b) has the same sequence as a fragment of intron 4 of the human HGF gene.

5. The hybrid HGF construct of claim 4 , wherein said hybrid HGF construct comprises SEQ ID NO:19.

6. The hybrid HGF construct of claim 4 , wherein said hybrid HGF construct comprises SEQ ID NO:20.

7. The hybrid HGF construct of claim 4 , wherein said hybrid HGF construct comprises SEQ ID NO:21.

8. A vector comprising the hybrid HGF construct of claim 1 .

9. The vector of claim 8 , wherein said vector further comprises one or more sequences for regulating expression, a self-replication sequence, or a secretory signal.

10. The vector of claim 9 , wherein said vector is selected from the group consisting of: pCK-HGF-X2, pCK-HGF-X3, pCK-HGF-X6, pCK-HGF-X7, pCK-HGF-X8, pCP-HGF-X2, pCPHGF-X3, pCP-HGF-X6, pCP-HGF-X7 and pCP-HGF-X8.

11. An isolated cell containing the vector of claim 8 , wherein said cell is a mammalian cell, a bacterial cell or a yeast cell.

12. The cell of claim 11 , wherein said cell is a mammalian cell.

13. The cell of claim 11 , wherein said cell is a yeast cell.

14. The cell of claim 11 , wherein said cell is an E. coli cell.

15. The cell of claim 14 , wherein said cell is an E. coli Top10F′ pCK-HGF-X7 (Deposit No. KCCM-10361) or E. coli Top10F′ pCP-HGF-X7 (Deposit No. KCCM-10362) cell.

16. A pharmaceutical composition comprising the hybrid HGF construct of claim 1 and a carrier.

17. A method of producing a hybrid HGF protein comprising culturing the cell of claim 11 in a suitable medium and collecting the hybrid HGF protein.

18. A hybrid HGF construct comprising a polynucleotide having a nucleotide sequence not less than 90% identical to SEQ ID NO:2, wherein the polynucleotide having said nucleotide sequence simultaneously encodes two heterotypes of human HGF.

19. The hybrid HGF construct of claim 18 , wherein said nucleotide sequence is not less than 95% identical to SEQ ID NO:2.

20. A hybrid HGF construct comprising a polynucleotide having a nucleotide sequence not less than 90% identical to SEQ ID NO:19, wherein the polynucleotide having said nucleotide sequence simultaneously encodes two heterotypes of human HGF.

21. The hybrid HGF construct of claim 20 , wherein said nucleotide sequence is not less than 95% identical to SEQ lID NO:19.

22. A hybrid HGF construct comprising a polynucleotide having a nucleotide sequence not less than 90% identical to SEQ ID NO:20, wherein the polynucleotide having said nucleotide sequence simultaneously encodes two heterotypes of human HGF.

23. The hybrid HGF construct of claim 22 , wherein said nucleotide sequence is not less than 95% identical to SEQ ID NO:20.

24. A hybrid HGF construct comprising a polynucleotide having a nucleotide sequence not less than 90% identical to SEQ ID NO:21, wherein the polynucleotide having said nucleotide sequence simultaneously encodes two heterotypes of human HGF.

25. The hybrid HGF construct of claim 24 , wherein said nucleotide sequence is not less than 95% identical to SEQ ID NO:21.

26. A vector comprising the hybrid HGF construct of claim 18 .

27. An isolated cell comprising the hybrid HGF construct of claim 18 , wherein said cell is a mammalian cell, a bacterial cell or a yeast cell.

28. A pharmaceutical composition comprising the hybrid HGF construct of claim 18 and a carrier.

29. A method of producing a hybrid HGF protein comprising culturing the cell of claim 27 in a suitable medium and collecting the hybrid HGF protein.

30. A vector comprising the hybrid HGF construct of claim 20 .

31. An isolated cell comprising the hybrid HGF construct of claim 20 , wherein said cell is a mammalian cell, a bacterial cell or a yeast cell.

32. A pharmaceutical composition comprising the hybrid HGF construct of claim 20 and a carrier.

33. A method of producing a hybrid HGF protein comprising culturing the cell of claim 31 in a suitable medium and collecting the hybrid HGF protein.

34. A vector comprising the hybrid HGF construct of claim 22 .

35. An isolated cell comprising the hybrid HGF construct of claim 22 , wherein said cell is a mammalian cell, a bacterial cell or a yeast cell.

36. A pharmaceutical composition comprising the hybrid HGF construct of claim 22 and a carrier.

37. A method of producing a hybrid HGF protein comprising culturing the cell of claim 35 in a suitable medium and collecting the hybrid HGF protein.

38. A vector comprising the hybrid HGF construct of claim 24 .

39. An isolated cell comprising the hybrid HGF construct of claim 24 , wherein said cell is a mammalian cell, bacterial cell or yeast cell.

40. A pharmaceutical composition comprising the hybrid HGF construct of claim 24 and a carrier.

41. A method of producing a hybrid HGF protein comprising culturing the cell of claim 39 in a suitable medium and collecting the hybrid HGF protein.

42. A hybrid HGF construct comprising:

(a) a first cDNA which has the same sequence as human HGF exons 1-4wherein said exons 1-4 are arranged in sequential order without an intron therebetween, or degenerates thereof which do not alter the amino acid sequence encoded by said first cDNA,

(b) a polynucleotide comprising 483-727 of SEQ ID NO: 2 and 5117-5423 of SEQ ID NO: 2, and

(c) a second cDNA which has the same sequence as human HGF exons 5-18 wherein said exons 5-18 are arranged in sequential order without an intron therebetween or degenerates thereof which do not alter the amino acid sequence encoded by said second cDNA;

wherein (b) is located between (a) and (c); and the HGF construct simultaneously encodes two heterotypes of human HGF.

43. The hybrid HGF construct of claim 42 , wherein said polynucleotide comprises 483-727 of SEQ ID NO: 2 and 4168-5423 of SEQ ID NO: 2 between exons 4 and 5.

44. The hybrid HGF construct of claim 43 , wherein said polynucleotide comprises 483-727 of SEQ ID NO: 2 and 3168-5423 of SEQ ID NO: 2 between exons 4 and 5.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S NAME FROM --HELIXMITH CO., LTD PREVIOUSLY RECORDED AT REEL: 049151 FRAME: 0562. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Nov 24, 2020
From: VIROMED CO., LTD
To: HELIXMITH CO., LTD
Reel/Frame 054511/0459 →
CHANGE OF NAME Recorded May 10, 2019
From: VIROMED CO., LTD.
To: HELIXMITH CO., LTD
Reel/Frame 049151/0562 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S COUNTRY FROM "KOREA, DEMOCRATIC PEOPLE'S REPUBLIC OF" TO --REPUBLIC OF KOREA-- PREVIOUSLY RECORDED ON REEL 023150 FRAME 0685. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT DOCUMENT. Recorded Jul 10, 2017
From: PARK, EUN-JIN
To: VIROMED CO., LTD.
Reel/Frame 043142/0269 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 26, 2009
From: PARK, EUN-JIN
To: VIROMED CO., LTD.
Reel/Frame 023150/0685 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2005
From: KIM, JONG-MOOK; HAHN, WOONG
To: VIROMED CO., LTD.
Reel/Frame 015579/0077 →
Priority Claims (1)
KR 10-2002-0015074 · Mar 20, 2002 · national
Continuity (2)
Continuation PCTKR030054800 · Mar 20, 2003
Related Publication 20050079581A1 · Apr 14, 2005