IP Library Patent Application 16130295
Patent Application
App. No. 16/130,295

PLANT GENOME MODIFICATION USING GUIDE RNA/CAS ENDONUCLEASE SYSTEMS AND METHODS OF USE

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Quick Facts
Patent No.
US None
App. No.
16/130,295
Abstract

Compositions and methods are provided for genome modification of a target sequence in the genome of a plant or plant cell. The methods and compositions employ a guide RNA/Cas endonuclease system to provide an effective system for modifying or altering target sites within the genome of a plant, plant cell or seed. Also provided are compositions and methods employing a guide polynucleotide/Cas endonuclease system for genome modification of a nucleotide sequence in the genome of a cell or organism, for gene editing, and/or for inserting or deleting a polynucleotide of interest into or from the genome of a cell or organism. Once a genomic target site is identified, a variety of methods can be employed to further modify the target sites such that they contain a variety of polynucleotides of interest. Breeding methods and methods for selecting plants utilizing a two component RNA guide and Cas endonuclease system are also disclosed. Compositions and methods are also provided for editing a nucleotide sequence in the genome of a cell.

Claims (35)

1 .- 66 . (canceled)

67 . A method for modifying a target site in the genome of a maize cell, the method comprising:

a) providing to the maize cell a guide RNA and a Cas9 endonuclease, wherein said guide RNA and Cas9 endonuclease form a complex that enables the Cas9 endonuclease to introduce a double strand break at the target site; and,

b) identifying at least one maize cell that has a modification of the target site, wherein the modification is selected from the group consisting of: at least one nucleotide insertion, at least one nucleotide deletion, at least one nucleotide substitution, and any combination of the preceding.

68 . The method of claim 67 , wherein the guide RNA is introduced as a polyribonucleotide by particle bombardment.

69 . The method of claim 67 , wherein the guide RNA is introduced via particle bombardment or Agrobacterium transformation of a recombinant DNA construct comprising the corresponding guide DNA operably linked to a promoter.

70 . The method of claim 67 , wherein the Cas9 endonuclease is provided as a cas9 polynucleotide encoding a Cas9 polypeptide.

71 . The method of claim 67 , wherein the Cas9 endonuclease is plant-optimized.

72 . The method of claim 67 , wherein the Cas9 endonuclease is operably linked to a nuclear targeting signal and a nuclear localization signal.

73 . The method of claim 67 , wherein the target site is selected from the group consisting of: a promoter sequence, a terminator sequence, a regulatory element sequence, a splice site, a coding sequence, a polyubiquitination site, an intron site, and an intron-enhancing motif.

74 . The method of claim 67 , further comprising providing to the maize cell a polynucleotide modification template, wherein the polynucleotide modification template comprises at least one nucleotide modification as compared to the polynucleotide sequence of the target site.

75 . The method of claim 67 , further comprising providing to the maize cell a donor DNA, wherein the donor DNA comprises a polynucleotide of interest or a promoter.

76 . A method for modifying a target site in the genome of a soybean plant cell, the method comprising:

a) providing to the soybean cell a guide RNA and a Cas9 endonuclease, wherein said guide RNA and Cas9 endonuclease form a complex that enables the Cas9 endonuclease to introduce a double strand break at the target site; and,

b) identifying at least one soybean cell that has a modification of the target site, wherein the modification is selected from the group consisting of: at least one nucleotide insertion, at least one nucleotide deletion, at least one nucleotide substitution, and any combination of the preceding.

77 . The method of claim 76 , wherein the guide RNA is introduced as a polyribonucleotide by particle bombardment.

78 . The method of claim 76 , wherein the guide RNA is introduced via particle bombardment or Agrobacterium transformation of a recombinant DNA construct comprising the corresponding guide DNA operably linked to a promoter.

79 . The method of claim 76 , wherein the Cas9 endonuclease is provided as a cas9 polynucleotide encoding a Cas9 polypeptide

80 . The method of claim 76 , wherein the Cas9 endonuclease is plant-optimized.

81 . The method of claim 76 , wherein the Cas9 endonuclease is operably linked to a nuclear targeting signal and a nuclear localization signal.

82 . The method of claim 76 , wherein the target site is selected from the group consisting of: a promoter sequence, a terminator sequence, a regulatory element sequence, a splice site, a coding sequence, a polyubiquitination site, an intron site, and an intron-enhancing motif.

83 . The method of claim 76 , further comprising providing to the soybean cell a polynucleotide modification template, wherein the polynucleotide modification template comprises at least one nucleotide modification as compared to the polynucleotide sequence of the target site.

84 . The method of claim 76 , further comprising providing to the soybean cell a donor DNA, wherein the donor DNA comprises a polynucleotide of interest or a promoter.

85 . A maize cell comprising a Cas9 endonuclease and a guide RNA, wherein the Cas9 endonuclease and guide RNA form a complex that recognizes, binds to, and optionally creates a double strand break in a target sequence in the genome of the cell.

86 . The maize cell of claim 85 , wherein the Cas9 endonuclease is plant-optimized.

87 . The maize cell of claim 85 , wherein the guide RNA is present as a polyribonucleotide.

88 . The maize cell of claim 85 , wherein the guide RNA is present as a polynucleotide encoding a polyribonucleotide.

89 . The maize cell of claim 85 , wherein the Cas9 endonuclease is present as a polypeptide.

90 . The maize cell of claim 85 , wherein the Cas9 endonuclease is present as a polynucleotide encoding a Cas9 polypeptide.

91 . A soybean cell comprising a Cas9 endonuclease and a guide RNA, wherein the Cas9 endonuclease and guide RNA form a complex that recognizes, binds to, and optionally creates a double strand break in a target sequence in the genome of the cell.

92 . The soybean cell of claim 91 , wherein the Cas9 endonuclease is plant-optimized.

93 . The soybean cell of claim 91 , wherein the guide RNA is present as a polyribonucleotide.

94 . The soybean cell of claim 91 , wherein the guide RNA is present as a polynucleotide encoding a polyribonucleotide.

95 . The soybean cell of claim 91 , wherein the Cas9 endonuclease is present as a polypeptide.

96 . The soybean cell of claim 91 , wherein the Cas9 endonuclease is present as a polynucleotide encoding a Cas9 polypeptide.

Assignments (2)
NUNC PRO TUNC ASSIGNMENT Recorded Nov 29, 2022
From: E.I. DU PONT DE NEMOURS AND COMPANY
To: CORTEVA AGRISCIENCE LLC
Reel/Frame 063141/0155 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2019
From: CIGAN, ANDREW MARK; GAO, HUIRONG; LYZNIK, ALEKSANDER L.; SHI, JINRUI; SVITASHEV, SERGEI; YOUNG, JOSHUA K.; FALCO, SAVERIO CARL; LI, ZHONGSEN; LIU, ZHAN-BIN
To: PIONEER HI-BRED INTERNATIONAL, INC.; E.I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 048404/0024 →