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

Title: Methods of introducing nucleic acids into cellular DNA

Abstract

A method of introducing a nucleic acid sequence into a cell is provided where the cell has impaired or inhibited or disrupted DnaG primase activity or impaired or inhibited or disrupted DnaB helicase activity, or larger or increased gaps or distance between Okazaki fragments or lowered or reduced frequency of Okazaki fragment initiation, or the cell has increased single stranded DNA (ssDNA) on the lagging strand of the replication fork including transforming the cell through recombination with a nucleic acid oligomer.

Inventors:
; ; ;
Issue Date:
Research Org.:
Harvard Univ., Cambridge, MA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1632604
Patent Number(s):
10570400
Application Number:
15/426,527
Assignee:
President and Fellows of Harvard College (Cambridge, MA)
Patent Classifications (CPCs):
C - CHEMISTRY C12 - BIOCHEMISTRY C12N - MICROORGANISMS OR ENZYMES
DOE Contract Number:  
FG02-02ER63445
Resource Type:
Patent
Resource Relation:
Patent File Date: 02/07/2017
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; 59 BASIC BIOLOGICAL SCIENCES

Citation Formats

Lajoie, Marc J., Gregg, Christopher J., Mosberg, Joshua A., and Church, George M. Methods of introducing nucleic acids into cellular DNA. United States: N. p., 2020. Web.
Lajoie, Marc J., Gregg, Christopher J., Mosberg, Joshua A., & Church, George M. Methods of introducing nucleic acids into cellular DNA. United States.
Lajoie, Marc J., Gregg, Christopher J., Mosberg, Joshua A., and Church, George M. Tue . "Methods of introducing nucleic acids into cellular DNA". United States. https://www.osti.gov/servlets/purl/1632604.
@article{osti_1632604,
title = {Methods of introducing nucleic acids into cellular DNA},
author = {Lajoie, Marc J. and Gregg, Christopher J. and Mosberg, Joshua A. and Church, George M.},
abstractNote = {A method of introducing a nucleic acid sequence into a cell is provided where the cell has impaired or inhibited or disrupted DnaG primase activity or impaired or inhibited or disrupted DnaB helicase activity, or larger or increased gaps or distance between Okazaki fragments or lowered or reduced frequency of Okazaki fragment initiation, or the cell has increased single stranded DNA (ssDNA) on the lagging strand of the replication fork including transforming the cell through recombination with a nucleic acid oligomer.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Tue Feb 25 00:00:00 EST 2020},
month = {Tue Feb 25 00:00:00 EST 2020}
}

Works referenced in this record:

Conformational Adaptability of Redβ during DNA Annealing and Implications for Its Structural Relationship with Rad52
journal, August 2009


Rescue of arrested replication forks by homologous recombination
journal, July 2001


Mechanism of DNA chain growth. I. Possible discontinuity and unusual secondary structure of newly synthesized chains.
journal, February 1968


Multiplex automated genome engineering
patent, April 2012


Allelic exchange in Escherichia coli using the Bacillus subtilis sacB gene and a temperature-sensitive pSC101 replicon
journal, June 1991


Modified bases enable high-efficiency oligonucleotide-mediated allelic replacement via mismatch repair evasion
journal, May 2011


Genome-scale promoter engineering by coselection MAGE
journal, April 2012


Emergent Properties of Reduced-Genome Escherichia coli
journal, May 2006


Strand invasion promoted by recombination protein β of coliphage λ
journal, December 2004


Simple and highly efficient BAC recombineering using galK selection
journal, February 2005


Mutations in the Escherichia coli dnaG gene suggest coupling between DNA replication and chromosome partitioning
journal, February 1991


A nucleoside kinase as a dual selector for genetic switches and circuits
journal, November 2010


Identification of factors influencing strand bias in oligonucleotide‐mediated recombination in Escherichia coli
journal, November 2003


Single-stranded heteroduplex intermediates in λ Red homologous recombination
journal, January 2010


Single-molecule studies of fork dynamics in Escherichia coli DNA replication
journal, January 2008


High efficiency mutagenesis, repair, and engineering of chromosomal DNA using single-stranded oligonucleotides
journal, May 2001


The promiscuous primase
journal, October 2005


The Interaction between Helicase and Primase Sets the Replication Fork Clock
journal, August 1996


Precise Manipulation of Chromosomes in Vivo Enables Genome-Wide Codon Replacement
journal, July 2011


Crystal and Solution Structures of the Helicase-binding Domain of Escherichia coli Primase
journal, January 2005


Lambda Red Recombineering in Escherichia coli Occurs Through a Fully Single-Stranded Intermediate
journal, September 2010


The Extreme C Terminus of Primase Is Required for Interaction with DnaB at the Replication Fork
journal, August 1996


Improvement of recombination efficiency by mutation of Red proteins
journal, June 2005


Regulation of bacterial priming and daughter strand synthesis through helicase-primase interactions
journal, August 2006


Single-molecule analysis reveals that the lagging strand increases replisome processivity but slows replication fork progression
journal, August 2009


Enhanced levels of λ Red-mediated recombinants in mismatch repair mutants
journal, December 2003


Generating a synthetic genome by whole genome assembly: φX174 bacteriophage from synthetic oligonucleotides
journal, December 2003


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


Polymerase Exchange During Okazaki Fragment Synthesis Observed in Living Cells
journal, December 2011