IP Library Granted Patent US 9,315,806
Granted Patent B2
US 9,315,806 · App. 14/411,628 · Granted Apr 19, 2016

Massively parallel combinatorial genetics

Inventors: Timothy Kuan-Ta Lu (Charlestown, MA); Allen Cheng (Cambridge, MA)
Assignee: Massachusetts Institute of Technology
C12N15/1065C12N15/1027C12N15/1079C12Q1/6869G01N2035/00752
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Quick Facts
Patent No.
US 9,315,806
App. No.
14/411,628
Granted
Apr 19, 2016
Kind
B2
Abstract

The invention relates to methods and compositions that enable the rapid generation of high-order combinations of genetic elements, and that provide a barcoded basis for rapid characterization of the specific combination of genetic elements encoded within a single cell or in a pooled population.

Claims (75)

1. A genetic construct comprising:

a DNA element;

a first compatible end element and a second compatible end element flanking the DNA element, wherein the first and second compatible end elements are capable of annealing to each other;

a barcode element;

a third compatible end element and a fourth compatible end element flanking the barcode element, wherein the third and fourth compatible end elements are capable of annealing to each other but are not capable of annealing to the first or second compatible end elements; and

a separation site located between the fourth compatible end element and the first compatible end element, wherein the DNA element, first compatible end element and second compatible end element are on one side of the separation site, and the barcode element, third compatible end element and fourth compatible end element are on the other side of the separation site.

2. A genetic construct comprising:

a plurality of DNA elements;

a first compatible end element and a second compatible end element flanking the plurality of DNA elements, wherein the first and second compatible end elements are capable of annealing to each other;

a plurality of barcode elements;

a third compatible end element and a fourth compatible end element flanking the plurality of barcode elements, wherein the third and fourth compatible end elements are capable of annealing to each other but are not capable of annealing to the first or second compatible end elements; and

a separation site located between the plurality of DNA elements and the plurality of barcode elements.

3. A method for generating a combinatorial genetic construct, comprising:

providing a vector containing a first genetic construct according to claim 1 ;

cleaving the vector at the separation site within the first genetic construct, resulting in the first genetic construct being separated into first and second segments;

providing a second genetic construct according to claim 1 ; and

annealing the second genetic construct to the cleaved vector, wherein the annealing occurs at compatible end elements within the first and second genetic constructs that are capable of annealing to each other, and wherein after annealing, the second genetic construct is integrated between the first and second segments of the first genetic construct, creating a combinatorial genetic construct.

4. The method of claim 3 , wherein the method is iterative.

5. A method for identification of a DNA element or a plurality of DNA elements, comprising:

providing a genetic construct according to claim 1 ;

conducting an assay to determine the DNA sequence of the barcode or plurality of barcodes within the genetic construct and/or the DNA sequence of the DNA element or plurality of DNA elements within the genetic construct; and

identifying the DNA element or plurality of DNA elements.

6. A library comprising:

two or more genetic constructs according to claim 1 .

7. A method for generating a combinatorial genetic construct, comprising:

providing a vector comprising:

a first DNA element,

a first barcode element, and

two site-specific recombination elements located between the first DNA element and the first barcode element;

providing a first insert comprising:

a second DNA element,

a second barcode element, and

site-specific recombination elements flanking each of the second DNA element and the second barcode element, such that two site-specific recombination elements are located between the second DNA element and the second barcode element that are not compatible with the site-specific recombination elements within the vector, and two site-specific recombination elements are located outside of the second DNA element and the second barcode element that are compatible with the site-specific recombination elements within the vector;

conducting site specific recombination between the vector and the first insert, wherein the site specific recombination occurs between the site-specific recombination elements within the vector located between the first DNA element and the first barcode element and the compatible site-specific recombination elements within the first insert located outside of the second DNA element and the second barcode element, and wherein following site-specific recombination, the first insert is located within the vector, and the vector contains multiple DNA elements and multiple barcode elements, with two site-specific recombination elements located between the multiple DNA elements and the multiple barcode elements;

providing a second insert comprising:

a third DNA element,

a third barcode element, and

site-specific recombination elements flanking each of the third DNA element and the third barcode element, such that two site-specific recombination elements are located between the third DNA element and the third barcode element that are not compatible with the two site-specific recombination elements located between the multiple DNA elements and the multiple barcode elements of the vector, and two site-specific recombination elements are located outside of the third DNA element and the third barcode element that are compatible with the two site-specific recombination elements located between the multiple DNA elements and the multiple barcode elements of the vector;

conducting site specific recombination between the vector and the second insert, wherein the site specific recombination occurs between the site-specific recombination elements within the vector located between the multiple DNA elements and the multiple barcode elements and the compatible site-specific recombination elements within the second insert located outside of the third DNA element and the third barcode element, and wherein following site-specific recombination, the second insert is located within the vector, and the vector contains multiple DNA elements and multiple barcode elements, with two site-specific recombination elements located between the multiple DNA elements and the multiple barcode elements; and

repeating the site-specific recombination an n th number of times, alternating between site-specific recombination between the vector and the first insert and site-specific recombination between the vector and the second insert, thereby creating a combinatorial genetic construct.

8. A combinatorial genetic construct produced by the method of claim 7 .

9. A method for identification of a DNA element or a plurality of DNA elements, comprising:

providing a combinatorial genetic construct according to claim 8 ;

conducting an assay to determine the DNA sequence of one or more barcode elements within the combinatorial genetic construct and/or the DNA sequence of one or more DNA elements within the combinatorial genetic construct; and

identifying the DNA element or plurality of DNA elements.

10. A method for generating a combinatorial genetic construct, comprising:

providing a vector comprising:

a first DNA element,

a first barcode element, and

a recognition site for a first restriction enzyme located between the first DNA element and the first barcode element;

providing an insert comprising:

a second DNA element,

a second barcode element,

a recognition site for the first restriction enzyme located between the second DNA element and the second barcode element, and

two recognition sites for one or more restriction enzymes that are distinct from the first restriction enzyme located outside of the second DNA element and second barcode element, such that restriction digestion at the recognition site within the vector and at the two recognition sites located outside of the second DNA element and second barcode element within the insert generates compatible ends;

digesting the vector and insert with restriction enzymes;

annealing the insert to the vector, thereby producing a combinatorial genetic construct containing multiple DNA elements and multiple barcode elements; and

optionally repeating the method an n th number of times.

11. A combinatorial genetic construct produced by the method of claim 10 .

12. A method for identification of a DNA element or a plurality of DNA elements, comprising:

providing a combinatorial genetic construct according to claim 11 ;

conducting an assay to determine the DNA sequence of one or more barcode elements within the combinatorial genetic construct and/or the DNA sequence of one or more DNA elements within the combinatorial genetic construct; and

identifying the DNA element or plurality of DNA elements.

13. A method for generating a combinatorial genetic construct, comprising:

providing a vector containing a first genetic construct according to claim 2 ;

cleaving the vector at the separation site within the first genetic construct, resulting in the first genetic construct being separated into first and second segments;

providing a second genetic construct according to claim 2 ; and

annealing the second genetic construct to the cleaved vector, wherein the annealing occurs at compatible end elements within the first and second genetic constructs that are capable of annealing to each other, and wherein after annealing, the second genetic construct is integrated between the first and second segments of the first genetic construct, creating a combinatorial genetic construct.

14. The method of claim 13 , wherein the method is iterative.

15. A method for identification of a DNA element or a plurality of DNA elements, comprising:

providing a genetic construct according to claim 2 ;

conducting an assay to determine the DNA sequence of the barcode or plurality of barcodes within the genetic construct and/or the DNA sequence of the DNA element or plurality of DNA elements within the genetic construct; and

identifying the DNA element or plurality of DNA elements.

16. A library comprising:

two or more genetic constructs according to claim 2 .

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 16, 2018
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046548/0067 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2015
From: LU, TIMOTHY KUAN-TA; CHENG, ALLEN
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 035208/0981 →
Continuity (2)
Provisional Application 61666081 · Jun 29, 2012
Related Publication 20150141263A1 · May 21, 2015