DOE Patents title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Multiplex RNA-guided genome engineering

Abstract

Methods of multiplex genome engineering in cells using Cas9 is provided which includes a cycle of steps of introducing into the cell a first foreign nucleic acid encoding one or more RNAs complementary to the target DNA and which guide the enzyme to the target DNA, wherein the one or more RNAs and the enzyme are members of a co-localization complex for the target DNA, and introducing into the cell a second foreign nucleic acid encoding one or more donor nucleic acid sequences, and wherein the cycle is repeated a desired number of times to multiplex DNA engineering in cells.

Inventors:
;
Issue Date:
Research Org.:
Harvard Univ., Cambridge, MA (United States)
Sponsoring Org.:
USDOE; National Science Foundation (NSF)
OSTI Identifier:
1986637
Patent Number(s):
11459585
Application Number:
14/903,719
Assignee:
President and Fellows of Harvard College (Cambridge, MA)
Patent Classifications (CPCs):
C - CHEMISTRY C12 - BIOCHEMISTRY C12N - MICROORGANISMS OR ENZYMES
DOE Contract Number:  
0540879; FG02-02ER63445
Resource Type:
Patent
Resource Relation:
Patent File Date: 07/08/2014
Country of Publication:
United States
Language:
English

Citation Formats

Church, George M., and Dicarlo, James. Multiplex RNA-guided genome engineering. United States: N. p., 2022. Web.
Church, George M., & Dicarlo, James. Multiplex RNA-guided genome engineering. United States.
Church, George M., and Dicarlo, James. Tue . "Multiplex RNA-guided genome engineering". United States. https://www.osti.gov/servlets/purl/1986637.
@article{osti_1986637,
title = {Multiplex RNA-guided genome engineering},
author = {Church, George M. and Dicarlo, James},
abstractNote = {Methods of multiplex genome engineering in cells using Cas9 is provided which includes a cycle of steps of introducing into the cell a first foreign nucleic acid encoding one or more RNAs complementary to the target DNA and which guide the enzyme to the target DNA, wherein the one or more RNAs and the enzyme are members of a co-localization complex for the target DNA, and introducing into the cell a second foreign nucleic acid encoding one or more donor nucleic acid sequences, and wherein the cycle is repeated a desired number of times to multiplex DNA engineering in cells.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {2022},
month = {10}
}

Works referenced in this record:

High efficiency gene transfer into mamalian cells by a double transfection protocol
journal, January 1992


Positive And Negative Selectable Markers For Use In Thermophilic Organisms
patent-application, February 2013


A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity
journal, June 2012


Target DNA interference with crRNA
patent-application, March 2010


CRISPR adaptive immunity systems of prokaryotes
journal, April 2012


Safeguarding CRISPR-Cas9 gene drives in yeast
journal, November 2015


Functional Genomics Using CRISPR-Cas Systems, Compositions, Methods, Knock Out Libraries and Applications Thereof
patent-application, December 2014


Multiplex Genome Engineering Using CRISPR/Cas Systems
journal, January 2013


Yeast Oligo-Mediated Genome Engineering (YOGE)
journal, November 2013


RNA-guided editing of bacterial genomes using CRISPR-Cas systems
journal, January 2013


Highly Efficient Genome Modifications Mediated by CRISPR/Cas9 in Drosophila
journal, July 2013


Programming cells by multiplex genome engineering and accelerated evolution
journal, July 2009


One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering
journal, May 2013


Genome Engineering of Drosophila with the CRISPR RNA-Guided Cas9 Nuclease
journal, May 2013


Methods And Compositions For Rna-Directed Target Dna Modification And For Rna-Directed Modulation Of Transcription
patent-application, March 2014