IP Library Granted Patent US 10,519,468
Granted Patent B2
US 10,519,468 · App. 15/845,524 · Granted Dec 31, 2019

Cells containing CRISPR hybrid DNA/RNA polynucleotides

Inventors: Andrew Paul May (San Francisco, CA); Paul Daniel Donohoue (Berkeley, CA)
Assignee: PIONEER HI-BRED INTERNATIONAL, INC.
C12N15/907C12N9/16C12N9/22C12N15/111C12N15/63C12N15/8213C12N15/902C12Q1/6827C12Y301/00C12N2320/51C12N2320/53
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Quick Facts
Patent No.
US 10,519,468
App. No.
15/845,524
Granted
Dec 31, 2019
Kind
B2
Abstract

The present disclosure provides DNA-guided CRISPR systems; polynucleotides comprising DNA, RNA and mixtures thereof for use with CRISPR systems; and methods of use involving such polynucleotides and DNA-guided CRISPR systems.

Claims (12)

1. A cell comprising: (i) a first polynucleotide wherein the first polynucleotide comprises a targeting region and an activating region adjacent to said targeting region; and (ii) a second polynucleotide wherein the second polynucleotide comprises an activating region wherein the activating region comprises DNA and a sequence that is complementary to a sequence in said activating region of the first polynucleotide, wherein said activating region of the first polynucleotide and said activating region of the second polynucleotide are capable of hybridizing to each other to form an activating duplex region, and wherein said activating duplex region is capable of binding with a site-directed polypeptide selected from the group consisting of a Cas9, a Cas9 with reduced nuclease activity, a Cas9 with nickase activity, a Cas9 with no nuclease activity, and a fusion protein comprising a Cas9 domain, wherein the Cas9 domain is capable of binding with the activating duplex region and wherein the fusion protein further comprises a domain from a polypeptide other than Cas9.

2. The cell of claim 1 , wherein the cell further comprises a site-directed polypeptide selected from the group consisting of a Cas9, a Cas9 with reduced nuclease activity, a Cas9 with nickase activity, a Cas9 with no nuclease activity, and a fusion protein comprising a Cas9 domain, wherein the Cas9 domain is capable of binding with the activating duplex region and wherein the fusion protein further comprises a domain from a polypeptide other than Cas9.

3. The cell of claim 2 , wherein the site-directed polypeptide is encoded by an expression vector comprising a coding sequence for the site-directed polypeptide.

4. The cell of claim 2 , wherein the site-directed polypeptide is constitutively expressed by the cell.

5. The cell of claim 2 , wherein the site-directed polypeptide comprises a nuclear localization signal (NLS).

6. The cell of claim 2 , wherein the site-directed polypeptide is a Cas9 with no nuclease activity.

7. The cell of claim 2 , wherein the site-directed polypeptide is a Cas9 with reduced nuclease activity.

8. The cell of claim 2 , wherein the site-directed polypeptide is a fusion protein comprising a Cas9 domain, wherein the Cas9 domain is capable of binding with the activating duplex region and wherein the fusion protein further comprises a domain from a polypeptide other than Cas9 and which confers an additional activity on the site-directed polypeptide selected from the group consisting of nuclease activity, methyltransferase activity, demethylase activity, DNA repair activity, DNA damage activity, deamination activity, dismutase activity, alkylation activity, depurination activity, oxidation activity, pyrimidine dimer forming activity, integrase activity, transposase activity, recombinase activity, polymerase activity, ligase activity, helicase activity, photolyase activity, glycosylase activity, acetyltransferase activity, deacetylase activity, kinase activity, phosphatase activity, ubiquitin ligase activity, deubiquitinating activity, adenylation activity, deadenylation activity, SUMOylating activity, deSUMOylating activity, ribosylation activity, deribosylation activity, myristoylation activity and demyristoylation activity.

9. The cell of claim 1 , wherein the first and second polynucleotides are introduced into the cell by lipofection, electroporation, nucleofection, microinjection, biolistics, liposomes, immunoliposomes, polycation, lipid:nucleic acid conjugates, or combinations thereof.

10. The cell of claim 1 , wherein the cell is selected from the group consisting of a bacterial cell, an archaeal cell, a plant cell, an algal cell, a fungal cell, an invertebrate cell, a vertebrate cell, a mammalian cell, and a human cell.

11. The cell of claim 1 , wherein the activating duplex region comprises a compound selected from the group consisting of phosphorothioates, chiral phosphorothioates, phosphorodithioates, phosphotriesters, aminoalkylphosphotriesters, alkylphosphonates, 5′-alkylene phosphonates, chiral phosphonates, phosphinates, phosphoramidates, 3′-amino phosphoramidate, amino alkylphosphoramidates, phosphorodiamidates, thionophosphoramidates, thionoalkylphosphonates, thionoalkylphosphotriesters, selenophosphates, and boranophosphates.

12. The cell of claim 1 , further comprising a donor polynucleotide.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2021
From: PIONEER HI-BRED INTERNATIONAL, INC.
To: CARIBOU BIOSCIENCES, INC.
Reel/Frame 055250/0251 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2018
From: MAY, ANDREW PAUL; DONOHOUE, PAUL DANIEL
To: CARIBOU BIOSCIENCES, INC.
Reel/Frame 045325/0690 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2018
From: CARIBOU BIOSCIENCES, INC.
To: PIONEER HI-BRED INTERNATIONAL, INC.
Reel/Frame 045325/0749 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2018
From: CARIBOU BIOSCIENCES, INC.
To: PIONEER HI-BRED INTERNATIONAL, INC.
Reel/Frame 045688/0493 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2018
From: MAY, ANDREW PAUL; DONOHOUE, PAUL DANIEL
To: CARIBOU BIOSCIENCES, INC.
Reel/Frame 045688/0509 →
Continuity (6)
Continuation 15679555 · Aug 17, 2017
Continuation 15493744 · Apr 21, 2017
Continuation 15008054 · Jan 27, 2016
Provisional Application 62251548 · Nov 5, 2015
Provisional Application 62108931 · Jan 28, 2015
Related Publication 20180142263A1 · May 24, 2018
Cited By (1)
US 12,390,538