IP Library Granted Patent US 12,378,566
Granted Patent B2
US 12,378,566 · App. 18/055,614 · Granted Aug 5, 2025

Plant genome modification using guide RNA/Cas endonuclease systems and methods of use

Inventors: Andrew Mark Cigan (Madison, WI); Saverio Carl Falco (Wilmington, DE); Huirong Gao (Johnston, IA); Zhongsen Li (Hockessin, DE); Zhan-Bin Liu (Clive, IA); L. Aleksander Lyznik (Johnston, IA); Jinrui Shi (Johnston, IA); Sergei Svitashev (Johnston, IA); Joshua K. Young (Johnston, IA)
Assignees: PIONEER HI-BRED INTERNATIONAL, INC.; E.I. DU PONT DE NEMOURS AND COMPANY
C12N15/8213C12N15/00C12N15/63C12N15/8205C12N15/8207C12N15/8216C12N15/8247C12N15/8262A01H1/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,378,566
App. No.
18/055,614
Granted
Aug 5, 2025
Kind
B2
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 (20)

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

transforming at least one plant cell with a guide polynucleotide, a polynucleotide sequence encoding a Cas endonuclease, and an expression cassette encoding at least one developmental gene polypeptide, wherein the at least one developmental gene polypeptide comprises a Babyboom (BBM), an Ovule Development Protein 2 (ODP2), and/or a Wuschel (WUS) polypeptide, wherein the guide polynucleotide and the Cas endonuclease form a guide polynucleotide-Cas endonuclease complex that introduces a double-strand break at the target site in the plant cell, and wherein the at least one developmental gene polypeptide increases the frequency of modification of the target site by the guide polynucleotide-Cas endonuclease complex in the plant cell relative to a control plant cell comprising a guide polynucleotide-Cas endonuclease complex and not comprising an expression cassette encoding a developmental gene polypeptide; and

regenerating a plantlet or a plant from the plant cell, the plantlet or plant comprising a modified target site, wherein the plantlet or the plant does not contain the Cas endonuclease or the expression cassette encoding the at least one developmental gene polypeptide.

2. The method of claim 1 , wherein the at least one plant cell is an embryogenic plant cell.

3. The method of claim 2 , wherein the embryogenic plant cell is transformed by particle bombardment.

4. The method of claim 2 , wherein the at least one plant cell comprises a plurality of embryogenic plant cells and the double-strand break at the target site is induced in the plurality of embryogenic plant cells at a frequency of at least 10.1%.

5. The method of claim 1 , wherein the at least one plant cell is an embryo.

6. The method of claim 5 , wherein the embryo is transformed by particle bombardment or bacterial-mediated transformation.

7. The method of claim 5 , wherein the at least one plant cell comprises a plurality of embryos and the double-strand break at the target site is induced in the plurality of embryos at a frequency of at least 33%.

8. The method of claim 2 , wherein the modified target site comprises at least one nucleotide insertion, deletion, or substitution.

9. The method of claim 2 , wherein the modified target site is a promoter sequence, a terminator sequence, a regulatory element sequence, a splice site, a coding sequence, a polyubiquitination site, an intron site, an intron-enhancing motif, or a gene of interest.

10. The method of claim 2 , wherein the plant cell is monocot or dicot.

11. The method of claim 10 , wherein the monocot is maize, rice, sorghum, rye, barley, wheat, millet, oats, sugarcane, turfgrass, or switchgrass.

12. The method of claim 10 , wherein the dicot is soybean, canola, alfalfa, sunflower, cotton, tobacco, peanut, potato, Arabidopsis , or safflower.

13. The method of claim 2 , further comprising transforming the at least one plant cell with a polynucleotide modification template comprising at least one nucleotide modification relative to a polynucleotide sequence of the target site.

14. The method of claim 2 , wherein the polynucleotide sequence encoding the Cas endonuclease comprises a Cas coding region that is operably linked to a first nuclear localization signal upstream of the Cas coding region and a second nuclear localization signal downstream of the Cas coding region, wherein the first nuclear localization signal and the second nuclear localization signal are derived from different sources.

15. The method of claim 14 , wherein the first nuclear localization signal is a monopartite nuclear localization signal.

16. The method of claim 14 , wherein the second nuclear localization signal is a bipartite nuclear localization signal.

17. The method of claim 1 , wherein the plant cell is a non-protoplast plant cell.

18. The method of claim 1 , wherein the plant cell is transformed with the one or more expression cassettes by particle bombardment or bacterial-mediated transformation.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2025
From: CIGAN, ANDREW MARK; GAO, HUIRONG; FALCO, SAVERIO CARL; LI, ZHONGSEN; LIU, ZHAN-BIN; LYZNIK, LESZEK ALEKSANDER; SHI, JINRUI; SVITASHEV, SERGEI; YOUNG, JOSHUA K.
To: PIONEER HI-BRED INTERNATIONAL, INC.
Reel/Frame 070796/0001 →
Continuity (7)
Continuation 14913614
Provisional Application 62023239 · Jul 11, 2014
Provisional Application 61953090 · Mar 14, 2014
Provisional Application 61937045 · Feb 7, 2014
Provisional Application 61882532 · Sep 25, 2013
Provisional Application 61868706 · Aug 22, 2013
Related Publication 20230323374A1 · Oct 12, 2023
References Cited (400)
US 5036006A · Sanford et al. · 1991 [cited by applicant]
US 5639947A · Hiatt · 1997 [cited by applicant]
US 5959177A · Hein et al. · 1999 [cited by applicant]
US 6410329B1 · Hansen et al. · 2002 [cited by applicant]
US 6518485B1 · Connett-Porceddu et al. · 2003 [cited by applicant]
US 6603061B1 · Armstrong et al. · 2003 [cited by applicant]
US 6627797B1 · Duvick et al. · 2003 [cited by applicant]
US 7292055B2 · Egitto et al. · 2007 [cited by applicant]
US 7868149B2 · Boukharov et al. · 2011 [cited by applicant]
US 8012752B2 · Jayakumar et al. · 2011 [cited by applicant]
US 8124860B2 · Gallie et al. · 2012 [cited by applicant]
US 8575424B2 · Yau et al. · 2013 [cited by applicant]
US 8581036B2 · Samboju et al. · 2013 [cited by applicant]
US 8586361B2 · Tao et al. · 2013 [cited by applicant]
US 8609420B2 · Samuel et al. · 2013 [cited by applicant]
US 8653327B2 · Samboju et al. · 2014 [cited by applicant]
US 8680366B2 · Eudes et al. · 2014 [cited by applicant]
US 8697359B1 · Zhang · 2014 [cited by applicant]
US 8722410B2 · Samuel et al. · 2014 [cited by applicant]
US 8771945B1 · Zhang · 2014 [cited by applicant]
US 8795965B2 · Zhang · 2014 [cited by applicant]
US 8865406B2 · Zhang · 2014 [cited by applicant]
US 8871445B2 · Cong et al. · 2014 [cited by applicant]
US 8889356B2 · Zhang · 2014 [cited by applicant]
US 8889418B2 · Zhang et al. · 2014 [cited by applicant]
US 8895308B1 · Zhang et al. · 2014 [cited by applicant]
US 8906616B2 · Zhang et al. · 2014 [cited by applicant]
US 8932814B2 · Cong et al. · 2015 [cited by applicant]
US 8945839B2 · Zhang · 2015 [cited by applicant]
US 8993233B2 · Zhang et al. · 2015 [cited by applicant]
US 8999641B2 · Zhang et al. · 2015 [cited by applicant]
US 9163284B2 · Liu et al. · 2015 [cited by applicant]
US 9187755B2 · Samuel et al. · 2015 [cited by applicant]
US 9382548B2 · Eudes et al. · 2016 [cited by applicant]
US 9476057B2 · Samuel et al. · 2016 [cited by applicant]
US 9493782B2 · Cigan et al. · 2016 [cited by applicant]
US 9518266B2 · Bruce et al. · 2016 [cited by applicant]
US 9719108B2 · Samuel et al. · 2017 [cited by applicant]
US 9840713B2 · Zhang · 2017 [cited by applicant]
US 9885033B2 · Joung et al. · 2018 [cited by applicant]
US 10113162B2 · Mathis et al. · 2018 [cited by applicant]
US 10227576B1 · Cameron et al. · 2019 [cited by applicant]
US 10287594B2 · Beetham et al. · 2019 [cited by applicant]
US 10329547B1 · Cameron et al. · 2019 [cited by applicant]
US 10519457B2 · Li et al. · 2019 [cited by applicant]
US 10557146B2 · Gao et al. · 2020 [cited by applicant]
US 10870859B2 · Li et al. · 2020 [cited by applicant]
US 11427830B2 · Li et al. · 2022 [cited by applicant]
US 20040034888A1 · Liu et al. · 2004 [cited by applicant]
US 20040231016A1 · Wang et al. · 2004 [cited by applicant]
US 20040235099A1 · Payne et al. · 2004 [cited by applicant]
US 20070083945A1 · Byrum et al. · 2007 [cited by applicant]
US 20070178593A1 · Miller et al. · 2007 [cited by applicant]
US 20070199095A1 · Allen et al. · 2007 [cited by applicant]
US 20080047031A1 · Tao et al. · 2008 [cited by applicant]
US 20090070891A1 · Foley et al. · 2009 [cited by applicant]
US 20090100536A1 · Adams et al. · 2009 [cited by applicant]
US 20090104700A1 · Samuel et al. · 2009 [cited by applicant]
US 20090111186A1 · Held et al. · 2009 [cited by applicant]
US 20090133152A1 · Lyznik · 2009 [cited by applicant]
US 20100076057A1 · Sontheimer et al. · 2010 [cited by applicant]
US 20100159598A1 · Jayakumar et al. · 2010 [cited by applicant]
US 20100311168A1 · Samuel et al. · 2010 [cited by applicant]
US 20100313293A1 · Albertsen et al. · 2010 [cited by applicant]
US 20110035836A1 · Eudes et al. · 2011 [cited by applicant]
US 20110165679A1 · Gordon-Kamm et al. · 2011 [cited by applicant]
US 20110203012A1 · Dotson et al. · 2011 [cited by applicant]
US 20110247100A1 · Samboju et al. · 2011 [cited by applicant]
US 20120023619A1 · Samboju et al. · 2012 [cited by applicant]
US 20120023620A1 · Yau et al. · 2012 [cited by applicant]
US 20120244569A1 · Samuel et al. · 2012 [cited by applicant]
US 20130011828A1 · Barrangou et al. · 2013 [cited by applicant]
US 20130157369A1 · Miller · 2013 [cited by applicant]
US 20130198888A1 · Falco et al. · 2013 [cited by applicant]
US 20130263324A1 · Lassner et al. · 2013 [cited by applicant]
US 20130326725A1 · Shukla et al. · 2013 [cited by applicant]
US 20140020131A1 · Bidney et al. · 2014 [cited by applicant]
US 20140068797A1 · Doudna et al. · 2014 [cited by applicant]
US 20140090113A1 · Cogan et al. · 2014 [cited by applicant]
US 20140096284A1 · Martin-Ortigosa et al. · 2014 [cited by applicant]
US 20140179006A1 · Zhang · 2014 [cited by applicant]
US 20140179770A1 · Zhang et al. · 2014 [cited by applicant]
US 20140182012A1 · Eudes et al. · 2014 [cited by applicant]
US 20140186843A1 · Zhang et al. · 2014 [cited by applicant]
US 20140186919A1 · Zhang et al. · 2014 [cited by applicant]
US 20140186958A1 · Zhang · 2014 [cited by examiner]
US 20140189896A1 · Zhang et al. · 2014 [cited by applicant]
US 20140196170A1 · Qiao et al. · 2014 [cited by applicant]
US 20140227787A1 · Zhang · 2014 [cited by applicant]
US 20140234972A1 · Zhang · 2014 [cited by applicant]
US 20140242664A1 · Zhang et al. · 2014 [cited by applicant]
US 20140242699A1 · Zhang · 2014 [cited by applicant]
US 20140242700A1 · Zhang et al. · 2014 [cited by applicant]
US 20140242702A1 · Chen et al. · 2014 [cited by applicant]
US 20140242703A1 · Samuel et al. · 2014 [cited by applicant]
US 20140248702A1 · Zhang et al. · 2014 [cited by applicant]
US 20140256046A1 · Zhang et al. · 2014 [cited by applicant]
US 20140273231A1 · Zhang et al. · 2014 [cited by applicant]
US 20140273232A1 · Zhang et al. · 2014 [cited by applicant]
US 20140273234A1 · Zhang et al. · 2014 [cited by applicant]
US 20140273235A1 · Voytas · 2014 [cited by applicant]
US 20140310830A1 · Zhang et al. · 2014 [cited by applicant]
US 20140335620A1 · Zhang et al. · 2014 [cited by applicant]
US 20140342456A1 · Mali et al. · 2014 [cited by applicant]
US 20140357530A1 · Zhang et al. · 2014 [cited by applicant]
US 20140370558A1 · Mathis et al. · 2014 [cited by applicant]
US 20150020223A1 · Zhang et al. · 2015 [cited by applicant]
US 20150044191A1 · Liu et al. · 2015 [cited by applicant]
US 20150044772A1 · Zhao · 2015 [cited by applicant]
US 20150059010A1 · Cigan et al. · 2015 [cited by applicant]
US 20150067922A1 · Yang · 2015 [cited by examiner]
US 20150079681A1 · Zhang · 2015 [cited by applicant]
US 20150082478A1 · Cigan et al. · 2015 [cited by applicant]
US 20150167000A1 · Voytas et al. · 2015 [cited by applicant]
US 20150167009A1 · D'Halluin · 2015 [cited by applicant]
US 20150184171A1 · D'Halluin · 2015 [cited by applicant]
US 20150225734A1 · Voytas · 2015 [cited by examiner]
US 20150284727A1 · Kim et al. · 2015 [cited by applicant]
US 20150291967A1 · Mathis et al. · 2015 [cited by applicant]
US 20160024524A1 · Joung et al. · 2016 [cited by applicant]
US 20160032297A1 · Deschamps et al. · 2016 [cited by applicant]
US 20160145631A1 · Voytas et al. · 2016 [cited by applicant]
US 20160168592A1 · Church et al. · 2016 [cited by applicant]
US 20160201072A1 · Cigan et al. · 2016 [cited by applicant]
US 20160208271A1 · Cigan et al. · 2016 [cited by applicant]
US 20160208272A1 · Cigan et al. · 2016 [cited by applicant]
US 20160251667A1 · Cigan et al. · 2016 [cited by applicant]
US 20160289691A1 · Beetham et al. · 2016 [cited by applicant]
US 20160304846A1 · Liu et al. · 2016 [cited by applicant]
US 20160340746A1 · Makarov et al. · 2016 [cited by applicant]
US 20170022521A1 · Samuel et al. · 2017 [cited by applicant]
US 20170029880A1 · Fang et al. · 2017 [cited by applicant]
US 20170166912A1 · Brower-Toland et al. · 2017 [cited by applicant]
US 20170183677A1 · Gao et al. · 2017 [cited by applicant]
US 20180002715A1 · Cigan et al. · 2018 [cited by applicant]
US 20180057832A1 · Li · 2018 [cited by applicant]
US 20180087104A1 · Joung et al. · 2018 [cited by applicant]
US 20180142263A1 · May et al. · 2018 [cited by applicant]
US 20180163203A1 · Bennett et al. · 2018 [cited by applicant]
US 20180230476A1 · Cigan et al. · 2018 [cited by applicant]
US 20180258417A1 · Cigan et al. · 2018 [cited by applicant]
US 20180258438A1 · Chaky et al. · 2018 [cited by applicant]
US 20180273960A1 · Cigan et al. · 2018 [cited by applicant]
US 20180282763A1 · Cigan et al. · 2018 [cited by applicant]
US 20180327785A1 · Cigan et al. · 2018 [cited by applicant]
US 20180346895A1 · Cigan et al. · 2018 [cited by applicant]
US 20180371479A1 · Cigan et al. · 2018 [cited by applicant]
US 20190040405A1 · Cigan et al. · 2019 [cited by applicant]
US 20190100745A1 · Cigan et al. · 2019 [cited by applicant]
US 20190100762A1 · Cigan et al. · 2019 [cited by applicant]
US 20190136248A1 · Cigan et al. · 2019 [cited by applicant]
US 20190161742A1 · Cigan et al. · 2019 [cited by applicant]
US 20190264232A1 · Hou et al. · 2019 [cited by applicant]
US 20200157554A1 · Cigan et al. · 2020 [cited by applicant]
US 20220177900A1 · Cigan et al. · 2022 [cited by applicant]
US 20220364107A1 · Gao et al. · 2022 [cited by applicant]
US 20230193304A1 · Li et al. · 2023 [cited by applicant]
US 20230235345A1 · Cigan et al. · 2023 [cited by applicant]
CN 103667338A · 2014 [cited by applicant]
DE 102015006335A1 · 2016 [cited by applicant]
WO 2005049842A2 · 2005 [cited by applicant]
WO 2007025097A2 · 2007 [cited by applicant]
WO WO2007084294A2 · 2007 [cited by applicant]
WO 2009042164A1 · 2009 [cited by applicant]
WO 2010011961A3 · 2010 [cited by applicant]
WO WO2010011961A2 · 2010 [cited by applicant]
WO WO2010077319A1 · 2010 [cited by applicant]
WO WO2011143124A2 · 2011 [cited by applicant]
WO 2012129373A2 · 2012 [cited by applicant]
WO WO2012164565A1 · 2012 [cited by applicant]
WO WO2013019411A1 · 2013 [cited by applicant]
WO WO2013066423A2 · 2013 [cited by applicant]
WO WO2013066805A1 · 2013 [cited by applicant]
WO WO2013068845A2 · 2013 [cited by applicant]
WO 2013098244A1 · 2013 [cited by applicant]
WO WO2013112686A1 · 2013 [cited by applicant]
WO 2013142578A1 · 2013 [cited by applicant]
WO WO2013138363A2 · 2013 [cited by applicant]
WO WO2013141680A1 · 2013 [cited by applicant]
WO WO2013173535A2 · 2013 [cited by applicant]
WO WO2013176772A1 · 2013 [cited by applicant]
WO WO2014004487A1 · 2014 [cited by applicant]
WO WO2014018423A2 · 2014 [cited by applicant]
WO WO2014039872A1 · 2014 [cited by applicant]
WO 2014065596A1 · 2014 [cited by applicant]
WO WO2014071006A1 · 2014 [cited by applicant]
WO 2014093479A1 · 2014 [cited by applicant]
WO 2014093635A1 · 2014 [cited by applicant]
WO WO2014089290A1 · 2014 [cited by applicant]
WO WO2014093595A1 · 2014 [cited by applicant]
WO WO2014093694A1 · 2014 [cited by applicant]
WO WO2014093712A1 · 2014 [cited by applicant]
WO WO2014093768A1 · 2014 [cited by applicant]
WO 2014144155A1 · 2014 [cited by applicant]
WO WO2014144288A1 · 2014 [cited by applicant]
WO WO2014144761A2 · 2014 [cited by applicant]
WO WO2014150624A1 · 2014 [cited by applicant]
WO WO2014164466A1 · 2014 [cited by applicant]
WO WO2014165825A2 · 2014 [cited by applicant]
WO 2014186686A2 · 2014 [cited by applicant]
WO WO2014194190A1 · 2014 [cited by applicant]
WO WO2015006294A2 · 2015 [cited by applicant]
WO WO2015006747A2 · 2015 [cited by applicant]
WO WO2015026883A1 · 2015 [cited by applicant]
WO WO2015026885A1 · 2015 [cited by applicant]
WO WO2015026886A1 · 2015 [cited by applicant]
WO WO2015026887A1 · 2015 [cited by applicant]
WO WO2015070083A1 · 2015 [cited by applicant]
WO WO2015071474A2 · 2015 [cited by applicant]
WO WO2015112896A2 · 2015 [cited by applicant]
WO WO2015131101A1 · 2015 [cited by applicant]
WO WO2015112896A9 · 2015 [cited by applicant]
WO WO2015189693A1 · 2015 [cited by applicant]
WO WO2016007347A1 · 2016 [cited by applicant]
WO WO2016033298A1 · 2016 [cited by applicant]
WO WO2016040030A1 · 2016 [cited by applicant]
WO WO2016149352A1 · 2016 [cited by applicant]
WO WO2016186946A1 · 2016 [cited by applicant]
WO WO2017015015A1 · 2017 [cited by applicant]
WO WO2017034971A1 · 2017 [cited by applicant]
WO WO2017062855A1 · 2017 [cited by applicant]
WO WO2017066497A2 · 2017 [cited by applicant]
WO WO2017070032A1 · 2017 [cited by applicant]
WO WO2017117395A1 · 2017 [cited by applicant]
WO WO2017132239A1 · 2017 [cited by applicant]
WO WO2017155714A1 · 2017 [cited by applicant]
WO WO2017155715A1 · 2017 [cited by applicant]
WO WO2017155717A1 · 2017 [cited by applicant]
WO WO2017212264A1 · 2017 [cited by applicant]
WO WO2017218185A1 · 2017 [cited by applicant]
WO WO2018172556A1 · 2018 [cited by applicant]
WO WO2018197495A1 · 2018 [cited by applicant]
WO WO2018197520A1 · 2018 [cited by applicant]
WO WO2019074841A1 · 2019 [cited by applicant]
WO WO2019084148A1 · 2019 [cited by applicant]
WO WO2019089808A1 · 2019 [cited by applicant]
WO WO2019168953A1 · 2019 [cited by applicant]
WO WO2019177978A1 · 2019 [cited by applicant]
WO WO2019217354A1 · 2019 [cited by applicant]
WO WO2019217358A1 · 2019 [cited by applicant]
WO WO2019217816A1 · 2019 [cited by applicant]
Deng et al.. A novel method for induction of plant regeneration via somatic embryogenesis. Plant Science. vol. 177, Issue Jul. 1, 2009, pp. 43-48. (Year: 2009). [cited by examiner]
Srinivasan et al. Heterologous expression of the Baby Boom AP2/ERF transcription factor enhances the regeneration capacity of tobacco ( [cited by examiner]
Wang et al. Genes controlling plant architecture. Curr. Opin. Biotechnol. Apr. 2006; 17(2):123-9. (Year: 2006). [cited by examiner]
Farrell. The Regulation of Gene Expression in Plants and Animals. Chapter 1 pp. 1-38 In Regulation of Gene Expression in Plants, Edited by Carole L. Bassett., 2007, Springer. (Year: 2007). [cited by examiner]
Zhiyong Mao et al., Comparison of nonhomologous end joining and homologous recombination in human cells, DNA Repair, 2008, 7:1765-1771. [cited by applicant]
Biserka Relic et al., Interaction of the DNA modifying proteins VirD1 and VirD2 of Agrobacterium tumefaciens: Analysis by subcellular localization in mammalian cells, Proc Natl Acad Sci, 2008, 95:9105-9110. [cited by applicant]
Alicja Ziemienowicz, Import of Agrobacterium T-DNA into plant nuclei: two distinct functions of VirD2 and VirE2 proteins, The Plant Cell, 2001, 13:369-383. [cited by applicant]
Bassett et al. Highly efficient targeted mutagenesis of Drosophila with the CRISPR/Cas9 system. Cell Rep. Jul. 11, 2013 ;4(1 ):220-8. Epub Jul. 1, 2013. (Year: 2013). [cited by applicant]
Cai et al. Optimizing the codon usage of synthetic gene with QPSO algorithm. J. Theor. Biol. Sep. 7, 2008;254(1):123-7. Epub May 17, 2008. (Year: 2008). [cited by applicant]
Dale et al. Intra- and intermolecular site-specific recombination in plant cells mediated by bacteriophage P1 recombinase. Gene. Jul. 2, 1990;91(1):79-85. (Year: 1990). [cited by applicant]
Damm et al. Efficient transformation of Arabidopsis thaliana using direct gene transfer to protoplasts. Mol. Gen. Genet. May 1989; 217(1):6-12. (Year: 1989). [cited by applicant]
Durai et al. Zinc finger nucleases: custom-designed molecular scissors for genome engineering of plant and mammalian cells. Nucleic Acids Res. 2005; 33(18): 5978-5990. (Year: 2005). [cited by applicant]
Dudas et al. DNA double-strand break repair by homologous recombination Mu tat. Res. Mar. 2004,566(2): 131-67. (Year: 2004). [cited by applicant]
Friedland et al. Heritable genome editing in C.elegans via a CRISPR-Cas9 system. Nat. Methods. Aug. 2013; 10 (8):741-3. Epub Jun. 3, 20130. (Year: 2013). [cited by applicant]
Gordon-Kamm et al. Transformation of Maize Cells and Regeneration of Fertile Transgenic Plants. The Plant Cell. Jul. 1990;2(7): 603-618. (Year: 1990). [cited by applicant]
Guerineau et al. Effect of two consensus sequences preceding the translation initiator codon on gene expression in blant protoplasts. Plant Mol. Biol. Feb. 1992;18(4):815-8. (Year: 1992). [cited by applicant]
Hiei et al. Efficient transformation of rice ( [cited by applicant]
Horsch et al. Inheritance of functional foreign genes in plants. Science. Feb. 3, 1984;223(4635):496-8. (Year: 1984). [cited by applicant]
Jiang et al. Successful transient expression of Cas9 and single guide RNA genes in Chlamydomonas reinhardtii. Eukaryot. Cell. Nov. 2014;13(11):1465-9. Epub Sep. 19, 2014. (Year: 2014). [cited by applicant]
Kilby et al. Plant J. FLP recombinase in transgenic plants: constitutive activity in stably transformed tobacco and generation of marked cell clones in [cited by applicant]
Klee et al. Agrobacterium-mediated plant transformation and its further applications to plant biology. Ann. Rev. Plant Physiol. 1987. 38:467-86. (Year: 1987). [cited by applicant]
Klein et al. High-velocity microprojectiles for delivering nucleic acids into living cells. Nature 327, 70-73 (1987). (Year: 1987). [cited by applicant]
Li et al. High-efficiency TALEN-based gene editing produces disease-resistant rice. Nat Biotechnol. May 7, 2012;30 (5):390-2, supplementary information. (Year: 2012). [cited by applicant]
Li et al. An improved rice transformation system using the biolistic method. Plant Cell Reports 12, 250-255 (1993). (Year: 1993). [cited by applicant]
Lloyd et al. Functional expression of the yeast FLP/FRT site-specific recombination system in Nicotiana tabacum. Mol. Gen Gent. Mar. 1994;242(6):653-7. (Year: 1994). [cited by applicant]
Luo et al. 'GM-gene-deletor': fused IoxP-FRT recognition sequences dramatically improve the efficiency of FLP or CRE recombinase on transgene excision from pollen and seed of tobacco plants. Plant Biotechnol. J. Mar. 20… [cited by applicant]
Lyznik et al. Activity of yeast FLP recombinase in maize and rice protoplasts. Nucleic Acids Res. Feb. 25, 1993;21(4):969-75). (Year: 1993). [cited by applicant]
Maeser et al. The Gin recombinase of phage Mu can catalyse site-specific recombination in plant protoplasts. Mol. Gen. Genet. Nov. 1991;230(1-2):170-6. (Year: 1991). [cited by applicant]
Onouchi et al. Operation of an efficient site-specific recombination system of Zygosaccharomyces rouxii in tobacco cells. Nucleic Acids Res. Dec. 11, 1991;19(23):6373-8. (Year: 1991). [cited by applicant]
Puchta et al. Two different but related mechanisms are used in plants for the repair of genomic double-strand breaks by homologous recombination. Proc. Natl. Acad. Sci. U.S.A. May 14, 1996;93(10):5055-60. (Year: 1996). [cited by applicant]
Puchta et al. A transient assay in plant cells reveals a positive correlation between extrachromosomal recombination rates and length of homologous overlap. Nucleic Acids Research, vol. 19, Issue 10, May 11, 1991, pp. 2… [cited by applicant]
Puchta et al. Homologous recombination in plant cells is enhanced by in vivo induction of double strand breaks into DNA by a site-specific endonuclease. Nucleic Acids Res. Nov. 11, 1993 ;21 (22):5034-40. (Year: 1993). [cited by applicant]
Shukla et al. Precise genome modification in the crop species [cited by applicant]
Sugita et al. A transformation vector for the production of marker-free transgenic plants containing a single copy transgene at high frequency. Plant J. Jun. 2000;22(5):461-9. (Year: 2000). [cited by applicant]
Zhang et al. Transcription activator-like effector nucleases enable efficient plant genome engineering. Plant Physiol. Jan. 2013; 161 (1):20-7. Epub Nov. 2, 2012. (Year: 2013). [cited by applicant]
Zhang et al. A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes. Plant Methods. Sep. 30, 2011;7(1):30. (Year: 2011). [cited by applicant]
Li, Xueyuan; et al.: “Efficient Protoplast Regeneration Protocol and CRISPR/Cas9-Mediated Editing of Glucosinolate Transporter (GTR) Genes in Rapeseed ( [cited by applicant]
Mao, et al.: “Letter to the Editor; Application of the CRISPR-Cas System for Efficient Genome Engineering in Plants,” Molecular Plant, Nov. 2013 (Nov. 2013), vol. 6, No. 6, pp. 2008-2011. [cited by applicant]
Nekrasov, et al.: “Targeted mutagenesis in the model plant Nicotiana benthamiana using Cas9 RNA-guided endonuclease,” Nature Biotechnology, Aug. 2013 (Aug. 2013), vol. 31, No. 8, pp. 691-693. [cited by applicant]
Rodolphe Barrangou et al., CRISPR PRovides Acquired Resistance Against Viruses in Prokaryotes, Science, 2007, pp. 1709-1712, vol. 315. [cited by applicant]
Rodolphe Barrangou et al., RNA-mediated programmable DNA cleavage, Nature Biotechnology, Sep. 2012, pp. 836-838, vol. 30, No. 9. [cited by applicant]
Rodolphe Barrangou et al., CRISPR-Cas sytems and RNA-guided interference, WIREs RNA, 2013, pp. 267-278, vol. 4. [cited by applicant]
Khaoula Belhaj et al., Plant genome editing made easy: targeted mutagenesis in model and crop plants using the CRISPR/Cas system, Plant Methods, 2013, pp. 39-48, vol. 9. [cited by applicant]
Nannan Chang et al., Genome editing with RNA-guided Cas9 nuclease in Zebrafish embryos, Cell Research, 2013, pp. 465-472, vol. 23. [cited by applicant]
Seung Woo Cho et al., Targeted genome engineering in human cells with the Cas9 RNA-guided endonuclease, Nature Biotechnology, Mar. 2013, pp. 230-232, vol. 31, No. 3. [cited by applicant]
Krzysztof Chylinski et al., The tracrRNA and Cas9 families of type II CRISPR-Cas immunity systems, RNA Biology, May 2013, pp. 726-737, vol. 10, No. 10. [cited by applicant]
Le Cong et al., Multiplex Genome Engineering Using CRISPR/Cas Systems, Sciencexpress Reports, Jan. 3, 2013, pp. 1-7, vol. 1. [cited by applicant]
Elitza Deltcheva et al., CRISPR RNA maturation by trans-encoded small RNA and host factor RNase III, Nature, Mar. 31, 2011, pp. 602-607, vol. 471. [cited by applicant]
Kathleen D'Halluin et al., Targeted molecular trait stacking in cotton through targeted double-strand break induction, Plant Biotechnology Journal, pp. 933-941, vol. 11. [cited by applicant]
James E. Dicarlo et al., Genome engineering in [cited by applicant]
Zhengyan Feng et al., Efficient genome editing in plants using a CRISPR/Cas system, Cell Research, 2013, pp. 1229-1232, vol. 23. [cited by applicant]
Yanfang Fu et al., Improving CRISPR-Cas nuclease specificity using truncated guide RNAs, Nature Biotechnology, Mar. 2014, vol. 32, No. 3. [cited by applicant]
Todd Funke et al., Structural Basis of Glyphosate Resistance Resulting from the Double Mutation Thr [cited by applicant]
Thomas Gaj et al., ZFN, Talen and CRISPR/Cas-based methods for genome engineering, Trends Biotechnology, Jul. 2013, pp. 397-405, vol. 31(7). [cited by applicant]
Josiane E. Garneau et al., The CRISPR/Cas bacterial immune system cleaves bacteriophase and plasmid DNA, Nature, 2010, pp. 67-71, vol. 468. [cited by applicant]
Giedrius Gasiunas et al., Cas9-crRNA ribonucleoprotein complex mediates specific DNA cleavage for adaptive immunity in bacteria, PNAS, Sep. 4, 2012, e2579-2586. [cited by applicant]
Luke A Gilbert et al., CRISPR-Mediated Modular RNA-Guided Regulation of Transcription in Eukaryotes, Cell, Jul. 18, 2013, pp. 442-451, vol. 154(2). [cited by applicant]
Scott J. Gratz et al., Genome Engineering of Drosophila with the CRISPR RNA-Guided Cas9 Nuclease, Aug. 2013, Genetics, pp. 1029-1035, vol. 194. [cited by applicant]
Daniel H. Haft et al., A Guild of 45 CRISPR-Associated (Cas) Protein Families and Multiple CRISPR/Cas Subtypes Exist in Prokaryotic Genomes, PLoS Computational Biology, Nov. 2005, pp. 474-483, vol. 1, Issue 6. [cited by applicant]
Caryn R. Hale et al. , RNA-Guided RNA Cleavage by a CRISPR RNA-Cas Protein Complex, Cell, Nov. 25, 2009, pp. 945-956, vol. 139. [cited by applicant]
Rachel E. Haurwitz et al., Sequence- and Structure-Specific RNA Processing by a CRISPR Endonuclease, Science, Sep. 10, 2010, pp. 1355-1358, vol. 329. [cited by applicant]
Philippe Horvath et al., Diversity, Activity, and Evolution of CRISPR Loci in [cited by applicant]
Philippe Horvath et al., CRISPR/Cas, the Immune System of Bacteria and Archaea, Science, Jan. 8, 2010, pp. 167-170, vol. 327. [cited by applicant]
Zhonggang Hou et al., Efficient genome engineering in human pluripotent stem cells using Cas9 from Neisseria meningitides, PNAS, Sep. 24, 2013, pp. 15644-15649, vol. 110, No. 39. [cited by applicant]
Patrick D. Hsu et al., DNA targeting specificity of RNA-guided Cas9 nucleases, Nature Biotechnology, Sep. 2013, pp. 827-834, vol. 31, No. 9. [cited by applicant]
Woong Y. Hwang et al., Efficient In Vivo Genome Editing Using RNA-Guided Nucleases, Nature Biotech, Mar. 2013, pp. 227-229, vol. 31, No. 3. [cited by applicant]
Kyle Jacoby et al., Expanding LAGLIDADG endonuclease scaffold diversity by rapidly surveying evolutionary sequence space, Nucleic Acids Research, Feb. 2012, pp. 4954-4964, vol. 40, No. 11. [cited by applicant]
Wenyan Jiang et al., RNA-guided editing of bacterial genomes using CRISPR-Cas systems, Nature Biotechnology, Mar. 2013, pp. 233, vol. 31, No. 3. [cited by applicant]
Martin Jinek et al., A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity, Science, Aug. 17, 2012, pp. 816-821, vol. 337. [cited by applicant]
Martin Jinek et al., RNA-programmed genome editing in human cells, eLife, 2013, e00471, pp. 1-9. [cited by applicant]
Ross A. Johnson et al., A rapid assay to quantify the cleavage efficiency of custom-designed nucleases in planta, Plant Mol Biol, 2013, pp. 207-221, vol. 82. [cited by applicant]
Eugene V. Koonin et al., CRISPR-CAS Evolution of an RNA-based adaptive immunity system in prokaryotes, RNA Biology, May 2013, pp. 679-686, vol. 10:5. [cited by applicant]
Jian-Feng Li et al., Multiplex and homologous recombination-mediated genome editing in Arabidopsis and Nicotiana benthamiana using guide RNA and Cas9, Nature Biotechnology, Aug. 2013, pp. 688-691, vol. 31, No. 8. [cited by applicant]
Michael R. Lieber et al., The Mechanism of Double-Strand DNA Break Repair by the Nonhomologous DNA End Joining Pathway, Annu Rev Biochem, 2010, pp. 181-211, vol. 79. [cited by applicant]
Ming Ma et al., A Guide RNA Sequence Design Platform for the CRISPR/Cas9 System for Model Organism Genomes, BioMed Research International, 2013, 4 pages, Article ID 270805. [cited by applicant]
Morgan L. Maeder et al., CRISPR RNA-guided activation of endogenous human genes, Nature Methods, Oct. 2013, pp. 977-979, vol. 10, No. 10. [cited by applicant]
Kira S. Makarova et al., Evolution and classification of the CRISPR-Cas systems, Nat Rev Microbiol, Jun. 2011, pp. 467-477, vol. 9(6). [cited by applicant]
Prashant Mali et al., RNA-Guided Human Genome Engineering via Cas9, Sciencexpress, Feb. 15, 2013, pp. 823-826, vol. 15, 339(6121). [cited by applicant]
Yanfei Mao et al., Application of the CRISPR-Cas System for Efficient Genome Engineering in Plants, Molecular Plant, Nov. 2013, pp. 2008-2011, vol. 6, No. 6. [cited by applicant]
Luciano A. Marraffini et al., CRISPR Interference Limits Horizontal Gene Transfer in Staphylococci by Targeting DNA, Science, Dec. 19, 2008, pp. 1843-1845, vol. 322(5909). [cited by applicant]
Luciano A. Marraffini et al., CRISPR interference: RNA-directed adaptive immunity in bacteria and archaea, Nat Rev Genet, Mar. 2010, pp. 181-190, vol. 11(3). [cited by applicant]
Jin Miao et al., Targeted mutagenesis in rice using CRISPR-Cas System, Cell Research, 2013, pp. 1233-1236, vol. 23. [cited by applicant]
Jeffrey C. Miller et al., A Tale nuclease architecture for efficient genome editing, Nature Biotechnology, Feb. 2011, pp. 143-148, vol. 29. [cited by applicant]
F. J. Mojica et al., Biological significance of a family of regularly spaced repeats in the genomes of Archaea, Bacteria and mitochondria, Molecular Microbiology, May 2000, pp. 244-246, vol. 36. [cited by applicant]
Vladimir Nekrasov et al., Targeted mutagenesis in the model plant [cited by applicant]
Nancy Podevin et al., Site-directed nucleases: a paradigm shift in predictable, knowledge-based plant breeding, Trends in Biotechnology, Jun. 2013, pp. 375-383, vol. 31, No. 6. [cited by applicant]
Lei S. Qi et al., Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression, Cell, Feb. 28, 2013, pp. 1173-1183, vol. 152(5). [cited by applicant]
Sivaprakash Ramalingam et al., A CRISPR way to engineer the human genome, Genome Biology, 2013, 4 pages, vol. 14:107. [cited by applicant]
Paul D. Sadowski, Site-specific genetic recombination: hops, flips, and flops, FASEB, 1993, pp. 760-767, vol. 7. [cited by applicant]
Neville E. Sanjana et al., A Transcription Activator-Like Effector (TALE) Toolbox for Genome Engineering, Nat. Protoc, 2012, pp. 171-192, vol. 7(1). [cited by applicant]
Rimantas Sapranauskas et al., The [cited by applicant]
Brian Sauer, Site-specific recombination: developments and applications, Current Opinion in Biotechnology, 1994, pp. 521-527, vol. 5. [cited by applicant]
Qiwei Shan et al., Targeted genome modification of crop plants using a CRISPR-Cas system, Nature Biotechnology, Aug. 2013, pp. 686-688, vol. 31, No. 8. [cited by applicant]
Bin Shen et al., Generation of gene-modified mice via Cas9/RNA-mediated gene targeting, Cell Research, May 2013, pp. 720-723, vol. 23, No. 5. [cited by applicant]
Bruno Tinland et al., The T-DNA-linked VirD2 protein contains two distinct functional nuclear localization signals, Proc. Natl. Acad. Sci, Aug. 1992, pp. 7442-7446, vol. 89. [cited by applicant]
John Van Der Oost, New Tool for Genome Surgery, Science, Feb. 15, 2013, pp. 768-770, vol. 339. [cited by applicant]
Daniel F. Voytas, Plant Genome Engineering with Sequence-Specific Nucleases, Annual Review of Plant Biology, pp. 327-350, vol. 64. [cited by applicant]
Jianbin Wang et al., Targeted gene addition to a predetermined site in the human genome using a ZFN-based nicking enzyme, Genome Research, 2012, pp. 1316-1326. [cited by applicant]
Haoyi Wang et al., One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering, Cell, May 9, 2013, pp. 910-918, vol. 153(4). [cited by applicant]
Blake Wiedenheft et al., RNA-guided genetic silencing systems in bacteria and archaea, Nature, Feb. 16, 2012, pp. 331-338, vol. 482. [cited by applicant]
Kabin Xie et al., RNA-Guided Genome Editing in Plants Using a CRISPR-Cas System, Nov. 2013, Molecular Plant, pp. 1975-1983, vol. 6, No. 6. [cited by applicant]
Peter R. Beetham, A tool for functional plant genomics: Chimeric RNA/DNA oligonucleotides cause in vivo gene-specific mutations, Proc. Natl., Acad. Sci USA, Plant Biology, Jul. 1999, pp. 8774-8778, vol. 96. [cited by applicant]
Prashant Mali et al., CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering, Nat. Biotechnol., Sep. 2013, pp. 833-838, vol. 31(9). [cited by applicant]
International Search Report and Written Opinion—PCT/US2014/051778—mailed Dec. 3, 2014. [cited by applicant]
International Search Report and Written Opinion—PCT/US2014/051780—mailed Dec. 9, 2014. [cited by applicant]
Xu R., et al., “Gene Targeting Using the Agrobacterium Tumefaciens-Mediated CRISPR-Cas System in Rice,” Rice, May 2014, vol. 7, No. 1, pp. 1-4. [cited by applicant]
Abler M.L., et al., “Control of mRNA Stability in Higher Plants,” Plant Molecular Biology, 1996, vol. 32, pp. 63-78. [cited by applicant]
Ainley W.M., et al., “Trait Stacking via Targeted Genome Editing,” Plant Biotechnology Journal, Aug. 19, 2013, vol. 11, No. 9, pp. 1126-1134, DOI:10.1111/pbi.12107, ISSN 1467-7644, XP055218224. [cited by applicant]
Ali Z., et al., “Efficient Virus-Mediated Genome Editing in Plants using the CRISPR/Cas9 system,” Molecular Plant, Aug. 2015, vol. 8, pp. 1288-1291. [cited by applicant]
Anders C., et al., “Structural Basis of PAM-Dependent Target DNA Recognition by the Cas9 Endonuclease,” Nature, Sep. 25, 2014, vol. 513, pp. 569-573. [cited by applicant]
Anonymous, “CRISPR-Cas9 Genome Engineering with Dharmacon Tm Edit-RTM Inducible Lentiviral Cas9 Nuclease,” Horizon technical manual, Apr. 2014, pp. 1-18, XP055967783. [cited by applicant]
Anonymous: “Hypothetical Protein [Lactobacillus reuteri]: NCBI Reference Sequence: WP_019251774.1,” Ncbi Protein, Jun. 29, 2013, 1 Page, XP055291687, [Retrieved on Jul. 27, 2016] Retrieved from URL: http://www.ncbi.nlm.… [cited by applicant]
Anonymous: “Lactobacillus Reuteri TD1, Complete Genome, NCBI Reference Sequence: NC_021872.1,” NCBI Nucleotide, Feb. 8, 2015, 592 Pages, XP055291935, [Retrieved on Jul. 28, 2016] Retrieved from URL: http://www.ncbi.nlm.… [cited by applicant]
Application Forum: “A Streamlined Method for the Production, Screening, and Application of sgRNAs for CRISPR/Cas9 Gene Editing,” Sponsored Paper, BioTechniques, 2014, vol. 57, No. 3, p. 157. [cited by applicant]
Avila-Garcia W.V., et al., “Target site Mutation Associated with Glufosinate resistance in Italian Ryegrass ( [cited by applicant]
Bae S., et al., “Cas-OFFinder: A Fast and Versatile Algorithm that Searches for Potential Off-Target sites of Cas9 RNA-Guided Endonucleases,” Bioinformatics, 2014, vol. 30, No. 10, pp. 1473-1475. [cited by applicant]
Baltes N.J., et al., “DNA Replicons for Plant Genome Engineering,” The Plant Cell, Jan. 2014, vol. 26, No. 1, pp. 151-163. [cited by applicant]
Barrangou R., et al., “CRISPR-Cas Systems: Prokaryotes Upgrade to Adaptive Immunity,” Molecular Cell, Apr. 24, 2014, vol. 54, pp. 234-244. [cited by applicant]
Barrett C.M., et al., “Unlocking Access to DNA in Chromatin,” Chemical Engineering Progress, Sep. 2018, vol. 114, No. 9, pp. 55-62. [cited by applicant]
Begemann M.B., et al., “Precise Insertion and Guided Editing of Higher Plant Genomes using Cpf1 CRISPR Nucleases,” BioRxiv, 2017, 16 Pages, DOI: http://dx.doi.orgi/10.1101/109983. [cited by applicant]
Beurdeley M., et al., “Compact Designer TALENs for Efficient Genome Engineering,” Nature Communications, Apr. 23, 2013, vol. 4, No. 1762, pp. 1-8. [cited by applicant]
Bollen Y., et al.: “How to Create State-of-The-Art Genetic Model Systems: Strategies for Optimal CRISPR-Mediated Genome Editing,” Nucleic Acids Research, 2018, vol. 46, No., 13, pp. 6435-6454. [cited by applicant]
Bolotin A., et al., “Clustered Regularly Interspaced Short Palindrome Repeats (CRISPRs) have Spacers of Extrachromosomal Origin,” Microbiology, Accepted on May 30, 2005, vol. 151, pp. 2551-2561. [cited by applicant]
Bolotin A., et al., “Complete Sequence and Comparative Genome Analysis of the Dairy Bacterium [cited by applicant]
Bondy-Denomy J., et al., “To Acquire or Resist: the Complex Biological Effects of CRISPR-Cas Systems,” Trends in Microbiology, Epub Feb. 26, 2014, Apr. 2014, vol. 22, No. 4, pp. 218-225. [cited by applicant]
Bortesi L., et al., “The CRISPR/Cas9 System for Plant Genome Editing and Beyond,” Biotechnology Advances, Jan. 1, 2015, vol. 33, No. 1, pp. 41-52, XP055217852. [cited by applicant]
Brief for Appellees for Appeal No. 2017-1907 submitted to the United States Court of Appeals for the Federal Circuit on Oct. 25, 2017, 80 pages. [cited by applicant]
Briner A.E., et al., “Guide RNA Functional Modules Direct Cas9 Activity and Orthogonality,” Molecular Cell, Oct. 23, 2014, vol. 56, No. 2, 16, pp. 333-339, 17 Pages, Supplemental Information. [cited by applicant]
Briner A.E., et al., “Guide RNA Functional Modules Direct Cas9 Activity and Orthogonality,” Molecular Cell, Oct. 23, 2014, vol. 56, No. 2, pp. 333-339. [cited by applicant]
Burstein D., et al., “New CRISPR-Cas Systems from Uncultivated Microbes,” Nature, Feb. 9, 2017, vol. 542, pp. 237-241 (plus supplementary material). [cited by applicant]
Byrum J.R., et al., “N_Geneseq Database,” Accession No. ARD65600, US 20070083945, Apr. 12, 2007, SEQ ID No. 147296. [cited by applicant]
Carte J., et al., “Cas6 is an Endoribonuclease that Generates Guide RNAs for Invader Defense in Prokaryotes,” Genes and Development, 2008, vol. 22, pp. 3489-3496. [cited by applicant]
Cenik E.S., et al., “Argonaute Proteins,” Current Biology, 2011, vol. 21, No. 12, pp. R446-R449. [cited by applicant]
Cermak T., et al., “A Multipurpose Toolkit to Enable Advanced Genome Engineering in Plants,” The Plant Cell, Jun. 2017, vol. 29, pp. 1196-1217. [cited by applicant]
Chai R., et al., “B-Glucan Synthase Gene Overexpression and B-glucans Overproduction in Pleurotus Ostreatus Using Poromoter Swapping,” PLoS One, Apr. 24, 2013, vol. 8, Issue 4, e61693. [cited by applicant]
Chang Y-J., et al., “Complete Genome Sequence of Acidaminococcus Fermentans Type Strain (VR4T),” Standards in Genomic Sciences, 2010, vol. 3, pp. 1-14. [cited by applicant]
Chen H., et al., “Promise and Issues of Genetically Modified Crops,” Current Opinion in Plant Biology, May 1, 2013, vol. 16, No. 2, pp. 255-260, DOI:10.1016/j.pbi.2013.03.007, ISSN 1369-5266, XP055070912. [cited by applicant]
Chen J.S., et al., “CRISPR-Cas12a Target Binding Unleashes Indiscriminate Single-Stranded DNase Activity,” Science, Apr. 27, 2018, vol. 360, pp. 436-439. [cited by applicant]
Chen S., et al., “Highly Efficient Mouse Genome Editing by CRISPR Ribonucleoprotein Electroporation of Zygotes,” The Journal of Biological Chemistry, US, Jul. 8, 2016, vol. 291, No. 28, pp. 14457-14467, DOI:10.1074/jbc.… [cited by applicant]
Cheng A.W., et al., “Multiplexed Activation of Endogenous Genes by CRISPR-on, an RNA-Guided Transcriptional Activator System,” Cell Research, Oct. 2013, vol. 23, No. 10, pp. 1163-1171. [cited by applicant]
Cho S.W., et al., “Analysis of Off-Target Effects of CRISPR/Cas-Derived RNA-Guided Endonucleases and Nickases,” Genome Research, 2014, vol. 24, pp. 132-141. [cited by applicant]
Christou P., et al., “Stable Transformation of Soybean Callus by DNA-Coated Gold Particles,” Plant Physiology, 1988, vol. 87, pp. 671-674. [cited by applicant]
Chylinski K., et al., “Classification and Evolution of Type II CRISPR-Cas Systems,” Nucleic Acids Research, Published on Apr. 11, 2014, vol. 42, No. 10, pp. 6091-6105. [cited by applicant]
Claesson M.J., et al., “Multireplicon Genome Architecture of Lactobacillus Salivarius,” Proceedings of the National Academy of Sciences, Apr. 25, 2006, vol. 103 No. 17, pp. 6718-6723. [cited by applicant]
Communication of a Notice of European Opposition & Opponents Submissions for European Application No. 14761478.8, Ref No. 417331 EPAXB/CX, dated Oct. 24, 2022, 31 Pages. [cited by applicant]
Database: “Cas9-CRISPR-Associated Endonuclease CAs9, Bacillus Cereus VD131—Cas9 Gene & Protein”, UniProt Database Entry: R8LDU5, Apr. 15, 2019, 3 Pages. [cited by applicant]
Database: “CRISPR-Associated Endonuclease Cas9, Lactobacillus Salivarius (Strain UCC118): Q1WVK1_LACS1”, UniProt, May 2, 2006, 2 Pages. [cited by applicant]
Database ENA: “Brevibacillus Laterosporus GI-9 Hnh Endonuclease Family Protein,” Database Accession No. CCF15452, 2012, XP002788584, Retrieved from EBI. [cited by applicant]
Database: “Using Cpf1 for CRISPR,” Benchling, Jan. 1, 2015, 4 Pages, Retrieved from URL: https://benchling.com/pub/cpf1, XP55396832. [cited by applicant]
Decision of EP Opposition Decision for EP3036327, Feb. 2020, 8 Pages. [cited by applicant]
Deyle D.R., et al., “Adeno-Associated Virus Vector Integration,” Current Opinion in Molecular Therapeutics, Aug. 2009, vol. 11, No. 4, pp. 442-447. [cited by applicant]
Djukanovic V., et al.,“Male-Sterile Maize Plants Produced by Targeted Mutagenesis of the Cytochrome P450-like Gene (MS26) Using a Re-Designed I-Crel Homing Endonuclease,” The Plant Journal, Nov. 5, 2013, vol. 76, No. 5,… [cited by applicant]
Djukic M., et al., “Genome Seqence of Brevibacillus Laterosporus LMG 15441, a Pathogen of Invertebrates, ”Journal of Bacteriology, American Society for Micorbiology, US, Oct. 2011, vol. 193, No. 19, pp. 5535-5536. [cited by applicant]
Dong D., et al., “The Crystal Structure of Cpf1 in complex with Crispr Rna,” Nature, 2016, 16 pages, doi:10.1038/nature17944. [cited by applicant]
Dong O.X., et al., “Targeted DNA Insertion in Plants,” The Proceedings of the National Academy of Sciences, Apr. 30, 2021, vol. 118 No. 22, e2004834117, 9 Pages. [cited by applicant]
Doudna J.A., et al., “The New Frontier of Genome Engineering with CRISPR-Cas9,” Science, Nov. 24, 2014, vol. 346, No. 6213, 11 Pages. [cited by applicant]
Dow L.E., et al., “Inducible in Vivo Genome Editing with CRISPR-Cas9,” Nature Biotechnology, Apr. 2005, vol. 33, No. 4, pp. 390-394, EPublished on Feb. 18, 2015. [cited by applicant]
Ellegaard K.M., et al., “Extensive Intra-phylotype Diversity in Lactobacilli and Bifidobacteria from the Honeybee Gut,” BMC Genomics, Apr. 2015, vol. 16, No. 1, Article No. 284, 22 pages. [cited by applicant]
Endo A., et al., “Efficient Targeted Mutagenesis of Rice and Tobacco Genomes Using Cpf1 From Francisella Novicida,” Nature Scientific Reports, 2016, vol. 6, 38169, 9 pages. [cited by applicant]