Literature DB >> 15459968

Unmodified oligodeoxynucleotides require single-strandedness to induce targeted repair of a chromosomal EGFP gene.

Frank Radecke1, Sarah Radecke, Klaus Schwarz.   

Abstract

BACKGROUND: A number of genetic defects in humans are due to point mutations in a single, often tightly regulated gene. Genetic treatment of such defects is preferably done by correcting only the altered base pair at the endogenous locus rather than by a gene replacement strategy involving viral vectors. Promisingly high repair rates have been achieved in some systems with the non-viral approach of transfecting chimeric RNA/DNA oligonucleotides (chimeraplasts). However, since this technique does not yet perform robustly, several parameters thought to be important in oligonucleotide-mediated gene repair were examined.
METHODS: A series of transgenic HEK-293 cell clones has been established harboring high or low copy numbers of a point-mutated 'enhanced green fluorescent protein' (EGFP) gene as the target. At the level of single living cells, repair efficiencies were measured by fluorescence-activated cell sorting (FACS) regarding topology (single-stranded, double-stranded), exonuclease protection (four phosphorothioate linkages at both ends), polarity (sense, antisense), and length (13mer, 19mer, 35mer, 69mer) of the oligonucleotide.
RESULTS: When targeting chromosomal loci, up to 0.2% corrected cells were obtained with single-stranded unmodified oligodeoxynucleotides, whereas a chimeraplast, its DNA analogue, and double-stranded DNA fragments were practically non-functional. Correction efficiencies correlated with target gene copy numbers. Modifying exonuclease resistance, polarity or length of single-stranded oligodeoxynucleotides did not enhance repair efficacy above the sub-percentage range.
CONCLUSIONS: Successful chromosomal reporter gene repair in HEK-293 cells required an oligodeoxynucleotide to be single-stranded. In concert with the gene copy number correlation, functional interaction between the repair molecule and the target site seems to be one bottleneck in targeted gene repair.

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Year:  2004        PMID: 15459968     DOI: 10.1002/jgm.613

Source DB:  PubMed          Journal:  J Gene Med        ISSN: 1099-498X            Impact factor:   4.565


  13 in total

1.  Reporter system for the detection of in vivo gene conversion: changing colors from blue to green using GFP variants.

Authors:  Jeffrey R Sommer; Jon Alderson; Goetz Laible; Robert M Petters
Journal:  Mol Biotechnol       Date:  2006-06       Impact factor: 2.695

2.  Zinc-finger nuclease-induced gene repair with oligodeoxynucleotides: wanted and unwanted target locus modifications.

Authors:  Sarah Radecke; Frank Radecke; Toni Cathomen; Klaus Schwarz
Journal:  Mol Ther       Date:  2010-01-12       Impact factor: 11.454

Review 3.  Oligo/polynucleotide-based gene modification: strategies and therapeutic potential.

Authors:  R Geoffrey Sargent; Soya Kim; Dieter C Gruenert
Journal:  Oligonucleotides       Date:  2011-03-21

4.  A comparison of synthetic oligodeoxynucleotides, DNA fragments and AAV-1 for targeted episomal and chromosomal gene repair.

Authors:  Xavier Leclerc; Olivier Danos; Daniel Scherman; Antoine Kichler
Journal:  BMC Biotechnol       Date:  2009-04-20       Impact factor: 2.563

5.  Regulation of Gene Editing Activity Directed by Single-Stranded Oligonucleotides and CRISPR/Cas9 Systems.

Authors:  Pawel Bialk; Natalia Rivera-Torres; Bryan Strouse; Eric B Kmiec
Journal:  PLoS One       Date:  2015-06-08       Impact factor: 3.240

6.  Oligonucleotide-mediated gene targeting in human hepatocytes: implications of mismatch repair.

Authors:  Olga Igoucheva; Vitali Alexeev; Helen Anni; Emanuel Rubin
Journal:  Oligonucleotides       Date:  2008-06

7.  Genome-wide Mapping of Off-Target Events in Single-Stranded Oligodeoxynucleotide-Mediated Gene Repair Experiments.

Authors:  Sarah Radecke; Klaus Schwarz; Frank Radecke
Journal:  Mol Ther       Date:  2017-09-15       Impact factor: 11.454

8.  Selection-independent generation of gene knockout mouse embryonic stem cells using zinc-finger nucleases.

Authors:  Anna Osiak; Frank Radecke; Eva Guhl; Sarah Radecke; Nadine Dannemann; Fabienne Lütge; Silke Glage; Cornelia Rudolph; Tobias Cantz; Klaus Schwarz; Regine Heilbronn; Toni Cathomen
Journal:  PLoS One       Date:  2011-12-14       Impact factor: 3.240

9.  Combinatorial gene editing in mammalian cells using ssODNs and TALENs.

Authors:  Bryan Strouse; Pawel Bialk; Rohina A Niamat; Natalia Rivera-Torres; Eric B Kmiec
Journal:  Sci Rep       Date:  2014-01-21       Impact factor: 4.379

Review 10.  Emerging gene editing strategies for Duchenne muscular dystrophy targeting stem cells.

Authors:  Carmen Bertoni
Journal:  Front Physiol       Date:  2014-04-21       Impact factor: 4.566

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