IP Library Granted Patent US 9,663,823
Granted Patent B2
US 9,663,823 · App. 14/329,984 · Granted May 30, 2017

Transcription biomarkers of biological responses and methods of use

Inventors: Shelley Force Aldred (Hayward, CA); Nathan D. Trinklein (Redwood City, CA); Michael Rose (Walnut Creek, CA); Patrick Collins (Millbrae, CA)
Assignee: SWITCHGEAR GENOMICS, INC.
C12Q1/6876C12Q1/6883C12Q1/6886C12Q2600/136C12Q2600/158
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Quick Facts
Patent No.
US 9,663,823
App. No.
14/329,984
Granted
May 30, 2017
Kind
B2
Abstract

This invention provides transcription regulatory control sequences, the activity of which function as biomarkers for a variety of biological responses. This invention also provides expression constructs in which a biomarker transcription regulatory sequence is operably linked with a sequence for a reporter. Cells that comprise these expression constructs can be used in assays to identify conditions that modulate activity of the biological response.

Claims (65)

1. A method for determining whether a test compound activates an NFkB-mediated response in a cell comprising:

a) exposing a plurality of no more than 100 collections of cells to a test compound, wherein the cells in each collection comprise an expression construct comprising a promoter operatively linked with a heterologous sequence encoding a reporter, wherein the promoter within each collection is the same and each collection has a different promoter, wherein a plurality of the promoters are NFkB biomarker promoters of different genes and are selected from:

(1) SEQ ID NO: 139 (IRF1); SEQ ID NO: 140 (TNFA1P3); SEQ ID NO: 142 (RELB); SEQ ID NO: 144 (IL8); SEQ ID NO: 145 (VCAM1); SEQ ID NO: 149 (CD40); SEQ ID NO: 151 (CSF1); and SEQ ID NO: 153 (NFKB2);

(2) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (1); and

(3) a fragment of at least 500 nucleotides of a sequence of (1);

b) measuring expression of the reporter; and

c) correlating the measurement with an NFkB-mediated response, wherein increased expression of the reporter compared to a control, indicates that the test compound induces an NFkB-mediated response and decreased expression of the reporter compared with a control indicates that the test compound inhibits an NFkB-mediated response.

2. The method of claim 1 further comprising

i) measuring the activity of the reporter in the absence of the test compound or under a control compound;

ii) measuring the activity of the reporter in the presence of the test compound;

iii) measuring the difference or ratio of reporter activity between the cells exposed to the test compound and cells that were not; and

iv) correlating the difference or ratio between treated and untreated measurements with an NFkB-mediated response.

3. The method of claim 1 wherein the test compound is a small organic molecule having a size up to about 5000 Da.

4. The method of claim 1 wherein the test compound is a nucleic acid derivative selected from a small interfering RNA, a micro RNA mimic and a micro RNA inhibitor.

5. The method of claim 1 wherein the expression construct is comprised in a plasmid, a virus, a transposon vector, or an artificial chromosome vector.

6. The method of claim 1 wherein the expression construct is integrated into a chromosome in the cell.

7. The method of claim 1 wherein the reporter is a light-emitting reporter, a fluorescent reporter or a colorimetric reporter.

8. The method of claim 1 wherein the reporter is luciferase.

9. The method of claim 1 wherein one of the NFkB biomarker promoters is selected from:

(I) SEQ ID NO. 139 (IRF1);

(II) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (I); and

(III) a fragment of at least 500 nucleotides of a sequence of (I).

10. The method of claim 1 wherein one of the NFkB biomarker promoters is SEQ ID NO. 139 (IRF1).

11. The method of claim 1 wherein one of the NFkB biomarker promoters is selected from:

(I) SEQ ID NO. 140 (TNFA1P3);

(II) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (I); and

(III) a fragment of at least 500 nucleotides of a sequence of (I).

12. The method of claim 1 wherein one of the NFkB biomarker promoters is SEQ ID NO. 140 (TNFA1P3).

13. The method of claim 1 wherein one of the NFkB biomarker promoters is selected from:

(I) SEQ ID NO. 142 (RELB);

(II) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (I); and

(III) a fragment of at least 500 nucleotides of a sequence of (I).

14. The method of claim 1 wherein one of the NFkB biomarker promoters is SEQ ID NO. 142 (RELB).

15. The method of claim 1 wherein one of the NFkB biomarker promoters is selected from:

(I) SEQ ID NO. 144 (IL8);

(II) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (I); and

(III) a fragment of at least 500 nucleotides of a sequence of (I).

16. The method of claim 1 wherein one of the NFkB biomarker promoters is SEQ ID NO. 144 (IL8).

17. The method of claim 1 wherein one of the NFkB biomarker promoters is selected from:

(I) SEQ ID NO. 145 (VCAM1);

(II) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (I); and

(III) a fragment of at least 500 nucleotides of a sequence of (I).

18. The method of claim 1 wherein one of the NFkB biomarker promoters is SEQ ID NO. 145 (VCAM1).

19. The method of claim 1 wherein one of the NFkB biomarker promoters is selected from:

(I) SEQ ID NO. 149 (CD40);

(II) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (I); and

(III) a fragment of at least 500 nucleotides of a sequence of (I).

20. The method of claim 1 wherein one of the NFkB biomarker promoters is SEQ ID NO. 149 (CD40).

21. The method of claim 1 wherein one of the NFkB biomarker promoters is selected from:

(I) SEQ ID NO. 151 (CSF1);

(II) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (I); and

(III) a fragment of at least 500 nucleotides of a sequence of (I).

22. The method of claim 1 wherein one of the NFkB biomarker promoters is SEQ ID NO. 151 (CSF1).

23. The method of claim 1 wherein one of the NFkB biomarker promoters is selected from:

(I) SEQ ID NO. 153 (NFKB2);

(II) a sequence of at least 500 nucleotides having at least 98% sequence identity to a sequence of (I); and

(III) a fragment of at least 500 nucleotides of a sequence of (I).

24. The method of claim 1 wherein one of the NFkB biomarker promoters is SEQ ID NO. 153 (NFKB2).

25. The method of claim 1 comprising at least 5 different biomarker promoters.

26. The method of claim 1 wherein the selected expression constructs comprise an expression control sequence from each of the genes: IRF1, TNFA1P3, RELB, IL8, VCAM1, CD40, CSF1 and NFKB2.

27. The method of claim 1 , wherein the NFkB biomarker promoters are selected from (1) SEQ ID NO. 139 (IRF1); SEQ ID NO. 140 (TNFA1P3); SEQ ID NO. 142 (RELB); SEQ ID NO. 144 (IL8); SEQ ID NO. 145 (VCAM1); SEQ ID NO. 149 (CD40); SEQ ID NO. 151 (CSF1); and SEQ ID NO. 153 (NFKB2).

28. The method of claim 1 , wherein (a)(2) is a sequence and (a)(3) is a fragment of at least 700 nucleotides.

29. The method of claim 1 , wherein (a)(2) is a sequence and (a)(3) is a fragment of at least 900 nucleotides.

30. The method of claim 1 , wherein the sequence identity is at least 99.5%.

31. The method of claim 1 , wherein the plurality is no more than 50 collections of cells.

Assignments (4)
SECURITY INTEREST Recorded Aug 10, 2024
From: ACTIVE MOTIF, INC.
To: MIDCAP FINANCIAL TRUST
Reel/Frame 068244/0975 →
CORRECTIVE ASSIGNMENT TO CORRECT THE TYPOGRAPHICAL ERROR OF A PATENT NUMBER FROM 6993823 TO 9663823 PREVIOUSLY RECORDED ON REEL 042883 FRAME 0369. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER . Recorded Aug 29, 2017
From: SWITCHGEAR GENOMICS, INC.
To: ACTIVE MOTIF, INC.
Reel/Frame 043569/0656 →
MERGER Recorded Jul 3, 2017
From: SWITCHGEAR GENOMICS, INC.
To: ACTIVE MOTIF, INC.
Reel/Frame 042883/0369 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2015
From: ALDRED, SHELLEY FORCE; TRINKLEIN, NATHAN D.; ROSE, MICHAEL; COLLINS, PATRICK
To: SWITCHGEAR GENOMICS, INC.
Reel/Frame 034755/0297 →
Continuity (2)
Division 12586131 · Sep 16, 2009
Related Publication 20140364336A1 · Dec 11, 2014