IP Library Granted Patent US 10,672,501
Granted Patent B2
US 10,672,501 · App. 15/678,142 · Granted Jun 2, 2020

Control approach to cell reprogramming

Inventors: Indika Rajapakse (Ann Arbor, MI); Geoff Patterson (Ann Arbor, MI); Scott Ronquist (Ann Arbor, MI)
Assignee: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
G16B5/00C12N5/0602C12Q1/6881G16B25/00C12N2501/60C12N2506/09C12Q2600/158
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Quick Facts
Patent No.
US 10,672,501
App. No.
15/678,142
Granted
Jun 2, 2020
Kind
B2
Abstract

A method is presented for reprogramming cells of a subject. As a starting point, a biological sample of a sample cell is received from the subject, where the sample cell has a given cell type. The method includes: determining gene expression data for the sample cell from the biological sample; receiving gene expression data for a target cell having a target cell type, where the target cell type differs from the given cell type; deriving a state transition matrix which models cell dynamics; computing a regulatory set for a given transcription factor, where the regulatory set quantifies influence of the given transcription factor on a genome; expressing reprogramming of the sample cell to the target cell with a state-space representation of a linear system; and solving for the input vector in the state-space representation.

Claims (31)

1. A method for reprogramming cells of a subject, comprising:

receiving a biological sample of a sample cell from the subject, where the sample cell has a given cell type;

determining gene expression data for the sample cell from the biological sample;

receiving gene expression data for a target cell having a target cell type, where the target cell type differs from the given cell type;

deriving a state transition matrix which models cell dynamics;

computing a regulatory set for a given transcription factor, where the regulatory set quantifies influence of the given transcription factor on a genome;

expressing reprogramming of the sample cell to the target cell with a state-space representation of a linear system, where the gene expression data for the target cell serves as an output vector in the state-space representation, the gene expression data for the sample cell serves as a state vector in the state-space representation, the regulatory set for the given transcription factor serves as an input matrix in the state-space representation, and an input vector in the state-space representation represents the given transcription factor;

solving for the input vector in the state-space representation; and

introducing the given transcription factor into a particular cell of the subject, where the particular cell has the given cell type.

2. The method of claim 1 wherein determining gene expression data for the cell includes grouping genes within same topologically associated domains; and forming the state vector from the grouped genes.

3. The method of claim 2 further comprises grouping genes within same topologically associated domains using chromosome conformation capture techniques.

4. The method of claim 1 wherein the gene expression data for the sample cell is further defined as RNA-seq data.

5. The method of claim 1 wherein computing a regulatory set for a given transcription factor further comprises computing a regulator set for each of a plurality of transcription factors and joining the plurality of regulatory sets to form the input matrix.

6. The method claim 1 wherein solving for the input vector further comprises determining values for the input vector that minimize distance between the sample cell and the target cell.

7. The method of claim 6 further comprises determining values for the input vector using a least squares method.

8. The method of claim 1 wherein expressing reprogramming of the sample cell includes defining the state-space representation at two or more discrete times, where the two or more discrete times signify different points in a cell cycle and the given transcription factor can be introduced into a cell at any of the two or more discrete times.

9. The method of claim 8 wherein solving for the input vector further comprises identifying a subset of transcription factors, determining each possible sequence in which the transcription factors in the subset of transcription factors can be introduced into a cell, and solving for the input vector for each possible sequence of transcription factors in the subset of transcription factors.

10. A method for reprogramming cells of a subject,

comprising:

determining gene expression data for a sample cell from the subject by grouping genes within same topologically associated domains, where the sample cell has a given cell type;

determining gene expression data for a target cell having a target cell type, where the target cell type differs from the given cell type;

deriving a state transition matrix which models cell dynamics;

computing a regulatory set for a given transcription factor, where the regulatory set quantifies influence of the given transcription factor on a genome;

expressing reprogramming of the sample cell to the target cell with a state-space representation of a linear system, where the gene expression data for the target cell serves as an output vector in the state-space representation, the gene expression data for the sample cell serves as a state vector in the state-space representation, the regulatory set for the given transcription factor serves as an input matrix in the state-space representation, and an input vector in the state-space representation represents the given transcription factor;

solving for the input vector in the state-space representation by determining values for the input vector that minimize distance between the sample cell and the target cell; and

introducing the given transcription factor into a particular cell of the subject, where the particular cell has the given cell type.

11. The method of claim 10 further comprises grouping genes within same topologically associated domains using chromosome conformation capture techniques.

12. The method of claim 10 wherein the gene expression data for the sample cell is further defined as RNA-seq data.

13. The method of claim 10 wherein computing a regulatory set for a given transcription factor further comprises computing a regulator set for each of a plurality of transcription factors and joining the plurality of regulatory sets to form the input matrix.

14. The method of claim 10 wherein expressing reprogramming of the sample cell includes defining the state-space representation at two or more discrete times, where the two or more discrete times signify different points in a cell cycle and the given transcription factor can be introduced into a cell at any of the two or more discrete times.

15. The method of claim 14 wherein solving for the input vector further comprises identifying a subset of transcription factors, determining each possible sequence in which the transcription factors in the subset of transcription factors can be introduced into a cell, and solving for the input vector for each possible sequence of transcription factors in the subset of transcription factors.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2019
From: PATTERSON, GEOFF; RONQUIST, SCOTT
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 048092/0850 →
CONFIRMATORY LICENSE Recorded Jul 16, 2018
From: HARVARD UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046548/0913 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2018
From: RAJAPAKSE, INDIKA
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 044729/0005 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2018
From: BROCKETT, ROGER
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 044729/0131 →
Continuity (2)
Provisional Application 62377050 · Aug 19, 2016
Related Publication 20180129775A1 · May 10, 2018