CRISPR editing to embed nucleic acid landing pads into genomes of live cells

Patent metadata

Field	Value
Publication number	US-11299731-B1
Application number	US-202117475267-A
Country	US
Kind code	B1
Filing date	Sep 14, 2021
Priority date	Sep 15, 2020
Publication date	Apr 12, 2022
Grant date	Apr 12, 2022

Abstract

The present disclosure relates to compositions, methods, modules and automated integrated instrumentation for multiplex delivery of “landing pad” edits into the genomes of a population of live cells. The landing pads then may be leveraged to insert very large DNA sequences into the genomes of the population of live cells.

First claim

I claim:

1. A method for multiplex insertion of large DNA payloads into a population of cells and identifying cells with a desired phenotype or genotype comprising the steps of:
designing and synthesizing a library of editing cassettes comprising landing pads, wherein the editing cassettes further comprise a gRNA comprising homology to a target sequence in the cells and a repair template comprising 5′ and 3′ homology arms flanking the landing pad;
inserting the library of editing cassettes into a vector backbone resulting in a library of editing vectors;
transforming the population of cells with the library of editing vectors;
allowing editing to take place in the population of cells to produce edited cells;
transforming the edited cells with vectors carrying large DNA payloads, wherein the vectors carrying large DNA payloads further comprise a coding sequence for a recombinase or a meganuclease under control of an inducible promoter;
inducing expression of the recombinase or meganuclease to insert the large DNA payloads into the landing pads; and
screening for cells comprising the desired phenotype or genotype.

2. The method of claim 1 , wherein the vectors carrying large DNA payloads comprise a coding sequence for a recombinase, the landing pads comprise a recognition sequence for the recombinase and the large DNA payloads comprise recognition sequences for the recombinase flanking the large DNA payload.

3. The method of claim 2 , wherein the recombinase is a cyclization recombination enzyme (Cre) and the landing pad and large DNA payload comprise lox recombination sites.

4. The method of claim 2 , wherein the recombinase is flippase and the landing pad and large DNA payload comprise flippase recognition targets (FRTs).

5. The method of claim 1 , wherein the vectors carrying large DNA payloads comprise a coding sequence for a meganuclease, the landing pads comprise a recognition sequence for the meganuclease, and the large DNA payloads further comprise homologous recombination sequences flanking the DNA playloads.

6. The method of claim 5 , wherein the meganuclease belongs to the LAGLIDADG family of nucleases.

7. The method of claim 6 , wherein the meganuclease is I-SceI.

8. The method of claim 6 , wherein the meganuclease is I-CreI.

9. The method of claim 6 , wherein the meganuclease is I-DmoI.

10. The method of claim 1 , wherein the editing cassettes further comprise a barcode.

11. The method of claim 1 , wherein the editing cassettes further comprise an amplification priming site at the 3′ end of the editing cassette.

12. The method of claim 1 , wherein the vectors carrying the large DNA payloads further comprise a selectable marker and the method further comprises a selection step between the allowing step and the transforming the editing cells step.

13. The method of claim 12 , wherein the selectable marker in the vectors carrying the large DNA payloads is different from a selectable marker in the editing cassettes.

14. The method of claim 1 , wherein the vectors carrying the large DNA payloads comprise the coding sequence of the recombinase or meganuclease under the control of an inducible promoter.

15. The method of claim 14 , wherein the inducible promoter is a pL promoter.

16. The method of claim 14 , wherein the inducible promoter is a pBAD promoter.

17. The method of claim 1 , wherein the vectors carrying large DNA payloads further comprise an origin of replication and a selectable marker.

18. The method of claim 1 , wherein the large DNA payloads are from 100 bp to 100 Kb in length.

19. The method of claim 18 , wherein the large DNA payloads are from 500 bp to 50 Kb in length.

20. The method of claim 1 , wherein the screening step comprises polymerase chain reaction (PCR) analysis with appropriate primer sets; a metabolic test; measurement of transcript level; a phenotypic assay; detection of a protein product using an antibody specific to the protein product;
or DNA sequencing of the integrated large DNA payload.

21. A method for multiplex insertion of large DNA payloads into a population of cells and identifying cells with a desired phenotype or genotype comprising the steps of:
designing and synthesizing a library of editing cassettes comprising landing pads wherein the landing pads comprise a recognition sequence for a recombinase and wherein the editing cassettes further comprise a gRNA comprising homology to a target sequence in the cells and a repair template comprising 5′ and 3′ homology arms flanking the landing pad;
inserting the library of editing cassettes into a vector backbone resulting in a library of editing vectors;
transforming the population of cells with the library of editing vectors;
allowing editing to take place in the population of cells to produce edited cells;
transforming the edited cells with vectors carrying large DNA payloads, wherein the vectors carrying large DNA payloads further comprise a coding sequence for the recombinase under control of an inducible promoter;
inducing expression of the recombinase to insert the large DNA payloads into the landing pads; and
screening for cells comprising the desired phenotype or genotype.

22. The method of claim 21 , wherein the recombinase is a cyclization recombination enzyme (Cre) and the landing pad and large DNA payload comprise lox recombination sites.

23. The method of claim 21 , wherein the recombinase is flippase and the landing pad and large DNA payload comprise flippase recognition targets (FRTs).

24. The method of claim 21 , wherein the editing cassettes further comprise an amplification priming site at the 3′ end of the editing cassette and wherein the vectors carrying the large DNA payloads further comprise a selectable marker and the method further comprises a selection step between the allowing step and the transforming the editing cells step.

25. A method for multiplex insertion of large DNA payloads into a population of cells and identifying cells with a desired phenotype or genotype comprising the steps of:
designing and synthesizing a library of editing cassettes comprising landing pads wherein the landing pads comprise a recognition sequence for a meganuclease and wherein the editing cassettes further comprise a gRNA comprising homology to a target sequence in the cells and a repair template comprising 5′ and 3′ homology arms flanking the landing pad;
inserting the library of editing cassettes into a vector backbone resulting in a library of editing vectors;
transforming the population of cells with the library of editing vectors;
allowing editing to take place in the population of cells to produce edited cells;
transforming the edited cells with vectors carrying large DNA payloads, wherein the vectors carrying large DNA payloads further comprise a coding sequence for the meganuclease under control of an inducible promoter;
inducing expression of the meganuclease to insert the large DNA payloads into the landing pads; and
screening for cells comprising the desired phenotype or genotype.

26. The method of claim 25 , wherein the meganuclease belongs to the LAGLIDADG family of nucleases.

27. The method of claim 26 , wherein the meganuclease is I-SceI.

28. The method of claim 26 , wherein the meganuclease is I-CreI.

29. The method of claim 26 , wherein the meganuclease is I-DmoI.

30. The meth

Assignees

• Inscripta Inc

Inventors

• Held Daniel

Classifications

• C40B40/06

  Libraries containing nucleotides or polynucleotides, or derivatives thereof · CPC title

• C12N15/1082

  Preparation or screening gene libraries by chromosomal integration of polynucleotide sequences, HR-, site-specific-recombination, transposons, viral vectors · CPC title

• C12N15/70

  Vectors or expression systems specially adapted for E. coli · CPC title

• C12N15/113 Primary

  Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; {Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing (when used in plants C12N15/8218)} · CPC title

• C12N15/102

  Mutagenizing nucleic acids · CPC title