Repositorium

What is a repositorium?

The repositorium is a searchable database that provides data on relevant articles from journals, company web pages and web pages of governmental agencies about studies/applications of genome-editing in model plants and agricultural crops in the period January 1996 to May 2018. Search options are article type, technique, plant, traits or free text. The repositorium is based on the systematic map of Dominik Modrzejewski et al., published in the journal environmental evidence. (Download article PDF).

Oligonucleotide-Mediated Genome Editing Provides Precision and Function to Engineered Nucleases and Antibiotics in Plants


Typ / Jahr

Journal Article / 2017

Autoren

Sauer, Noel J.; Narváez-Vásquez, Javier; Mozoruk, Jerry; Miller, Ryan B.; Warburg, Zachary J.; Woodward, Melody J.; Mihiret, Yohannes A.; Lincoln, Tracey A.; Segami, Rosa E.; Sanders, Steven L.; Walker, Keith A.; Beetham, Peter R.; Schöpke, Christian R.; Gocal, Greg F. W.

Abstract

Here, we report a form of oligonucleotide-directed mutagenesis for precision genome editing in plants that uses single-stranded oligonucleotides (ssODNs) to precisely and efficiently generate genome edits at DNA strand lesions made by DNA double strand break reagents. Employing a transgene model in Arabidopsis (Arabidopsis thaliana), we obtained a high frequency of precise targeted genome edits when ssODNs were introduced into protoplasts that were pretreated with the glycopeptide antibiotic phleomycin, a nonspecific DNA double strand breaker. Simultaneous delivery of ssODN and a site-specific DNA double strand breaker, either transcription activator-like effector nucleases (TALENs) or clustered, regularly interspaced, short palindromic repeats (CRISPR/Cas9), resulted in a much greater targeted genome-editing frequency compared with treatment with DNA double strand-breaking reagents alone. Using this site-specific approach, we applied the combination of ssODN and CRISPR/Cas9 to develop an herbicide tolerance trait in flax (Linum usitatissimum) by precisely editing the 5'-ENOLPYRUVYLSHIKIMATE-3-PHOSPHATE SYNTHASE (EPSPS) genes. EPSPS edits occurred at sufficient frequency that we could regenerate whole plants from edited protoplasts without employing selection. These plants were subsequently determined to be tolerant to the herbicide glyphosate in greenhouse spray tests. Progeny (C1) of these plants showed the expected Mendelian segregation of EPSPS edits. Our findings show the enormous potential of using a genome-editing platform for precise, reliable trait development in crop plants.

Keywords
3-Phosphoshikimate 1-Carboxyvinyltransferase/genetics; Adaptation, Physiological/drug effects; Alleles; Anti-Bacterial Agents/pharmacology; Arabidopsis/drug effects/genetics; Base Sequence; CRISPR-Cas Systems/genetics; Endonucleases/metabolism; Flax/genetics; gene editing; genetic engineering; Genetic Loci; Genome, Plant; Glycine/analogs & derivatives/toxicity; Glycopeptides/pharmacology; Green Fluorescent Proteins/metabolism; Oligonucleotides/metabolism; Plants, Genetically Modified; Protoplasts/drug effects/metabolism; Transcription Activator-Like Effector Nucleases/metabolism
Periodical
Plant physiology
Periodical Number
4
Page range
1917–1928
Volume
170
DOI
10.1104/pp.15.01696

Techniques

ID Corresponding Author
Country
Plant Species GE Technique
Sequence Identifier
Trait
Type of Alteration
Progress in Research
Key Topic
402 Gocal, Greg F.W.
USA
Arabidopsis thaliana Oligonucleotide-directed mutagenesis
BFP
blue fluorescent protein
PM
Basic research
Basic research
403 Gocal, Greg F.W.
USA
Arabidopsis thaliana TALENs
BFP
blue fluorescent protein
SDN1
Basic research
Basic research
404 Gocal, Greg F.W.
USA
Arabidopsis thaliana CRISPR/Cas9
BFP
blue fluorescent protein
SDN1
Basic research
Basic research
405 Gocal, Greg F.W.
USA
Linum usitatissimum CRISPR/Cas9
EPSPS
herbicide tolerance
SDN1
Market-oriented
Herbicide tolerance