Search for authorsSearch for similar articles
5
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Are the current gRNA ranking prediction algorithms useful for genome editing in plants?

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Introducing a new trait into a crop through conventional breeding commonly takes decades, but recently developed genome sequence modification technology has the potential to accelerate this process. One of these new breeding technologies relies on an RNA-directed DNA nuclease (CRISPR/Cas9) to cut the genomic DNA, in vivo, to facilitate the deletion or insertion of sequences. This sequence specific targeting is determined by guide RNAs (gRNAs). However, choosing an optimum gRNA sequence has its challenges. Almost all current gRNA design tools for use in plants are based on data from experiments in animals, although many allow the use of plant genomes to identify potential off-target sites. Here, we examine the predictive uniformity and performance of eight different online gRNA-site tools. Unfortunately, there was little consensus among the rankings by the different algorithms, nor a statistically significant correlation between rankings and in vivo effectiveness. This suggests that important factors affecting gRNA performance and/or target site accessibility, in plants, are yet to be elucidated and incorporated into gRNA-site prediction tools.

          Related collections

          Most cited references13

          • Record: found
          • Abstract: found
          • Article: not found

          Plant genome editing made easy: targeted mutagenesis in model and crop plants using the CRISPR/Cas system

          Targeted genome engineering (also known as genome editing) has emerged as an alternative to classical plant breeding and transgenic (GMO) methods to improve crop plants. Until recently, available tools for introducing site-specific double strand DNA breaks were restricted to zinc finger nucleases (ZFNs) and TAL effector nucleases (TALENs). However, these technologies have not been widely adopted by the plant research community due to complicated design and laborious assembly of specific DNA binding proteins for each target gene. Recently, an easier method has emerged based on the bacterial type II CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated) immune system. The CRISPR/Cas system allows targeted cleavage of genomic DNA guided by a customizable small noncoding RNA, resulting in gene modifications by both non-homologous end joining (NHEJ) and homology-directed repair (HDR) mechanisms. In this review we summarize and discuss recent applications of the CRISPR/Cas technology in plants.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Cas-Designer: a web-based tool for choice of CRISPR-Cas9 target sites.

            We present Cas-Designer, a user-friendly program to aid researchers in choosing appropriate target sites in a gene of interest for type II CRISPR/Cas-derived RNA-guided endonucleases, which are now widely used for biomedical research and biotechnology. Cas-Designer rapidly provides the list of all possible guide RNA sequences in a given input DNA sequence and their potential off-target sites including bulge-type sites in a genome of choice. In addition, the program assigns an out-of-frame score to each target site to help users choose appropriate sites for gene knockout. Cas-Designer shows the results in an interactive table and provides user-friendly filter functions.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Initiation and maintenance of virus-induced gene silencing

              The phytoene desaturase (PDS) gene of Nicotiana benthamiana was silenced in plants infected with potato virus X (PVX) vectors carrying PDS inserts, and a green fluorescent protein (GFP) transgene was silenced in plants infected with PVX-GFP. This virus-induced gene silencing (VIGS) is post-transcriptional and cytoplasmic because it is targeted against exons rather than introns of PDS RNA and against viral RNAs. Although PDS and GFP RNAs are most likely targeted through the same mechanism, the VIGS phenotypes differed in two respects. PDS mRNA was targeted by VIGS in all green tissue of the PVX-PDS-infected plant, whereas PVX-PDS was not affected. In contrast, VIGS of the GFP was targeted against PVX-GFP. Initially, VIGS of the GFP was initiated in all green tissues, as occurred with PDS VIGS. However, after 30 days of infection, the GFP VIGS was no longer initiated in newly emerging leaves, although it was maintained in tissue in which it had already been initiated. Based on these analyses, we propose a model for VIGS in which the initiation of VIGS is dependent on the virus and maintenance of it is virus independent.
                Bookmark

                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: InvestigationRole: MethodologyRole: Project administrationRole: SupervisionRole: ValidationRole: Writing – original draftRole: Writing – review & editing
                Role: Data curationRole: InvestigationRole: Validation
                Role: Data curationRole: Formal analysisRole: InvestigationRole: Validation
                Role: Data curationRole: Formal analysisRole: InvestigationRole: Validation
                Role: Data curationRole: Formal analysis
                Role: InvestigationRole: Project administrationRole: Supervision
                Role: Data curationRole: Formal analysisRole: InvestigationRole: Methodology
                Role: ConceptualizationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: SupervisionRole: Writing – original draftRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                24 January 2020
                2020
                : 15
                : 1
                : e0227994
                Affiliations
                [1 ] Centre for Tropical Crops and Biocommodities, Science and Engineering Faculty, Queensland University of Technology, Brisbane, Queensland, Australia
                [2 ] Centre for Crop and Disease Management, School of Molecular and Life Sciences, Curtin University, Bentley, Western Australia, Australia
                [3 ] School of BioSciences, The University of Melbourne, Melbourne, Victoria, Australia
                [4 ] School of Mathematical Sciences, Science and Engineering Faculty, Queensland University of Technology, Brisbane, Queensland, Australia
                West China Hospital, Sichuan University, CHINA
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0001-8451-1104
                http://orcid.org/0000-0002-2812-3753
                Article
                PONE-D-19-29653
                10.1371/journal.pone.0227994
                6980586
                31978124
                ead0878e-c248-43c7-8c0c-d459cc0fdfa4
                © 2020 Naim et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 24 October 2019
                : 3 January 2020
                Page count
                Figures: 4, Tables: 0, Pages: 12
                Funding
                Funded by: ARC
                Award ID: FL160100155
                Award Recipient :
                FL160100155 awarded to PMW funded by Australian Research Council, The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and life sciences
                Biochemistry
                Nucleic acids
                RNA
                Guide RNA
                Biology and Life Sciences
                Plant Science
                Plant Anatomy
                Leaves
                Biology and Life Sciences
                Molecular Biology
                Molecular Biology Techniques
                Artificial Gene Amplification and Extension
                Polymerase Chain Reaction
                Research and Analysis Methods
                Molecular Biology Techniques
                Artificial Gene Amplification and Extension
                Polymerase Chain Reaction
                Research and Analysis Methods
                Database and Informatics Methods
                Bioinformatics
                Sequence Analysis
                Sequence Motif Analysis
                Biology and life sciences
                Biochemistry
                Proteins
                DNA-binding proteins
                Nucleases
                Biology and Life Sciences
                Biochemistry
                Enzymology
                Enzymes
                Hydrolases
                Nucleases
                Biology and Life Sciences
                Biochemistry
                Proteins
                Enzymes
                Hydrolases
                Nucleases
                Biology and Life Sciences
                Bioengineering
                Synthetic Bioengineering
                Genome Engineering
                Synthetic Genome Editing
                Crispr
                Engineering and Technology
                Bioengineering
                Synthetic Bioengineering
                Genome Engineering
                Synthetic Genome Editing
                Crispr
                Biology and Life Sciences
                Synthetic Biology
                Synthetic Bioengineering
                Genome Engineering
                Synthetic Genome Editing
                Crispr
                Engineering and Technology
                Synthetic Biology
                Synthetic Bioengineering
                Genome Engineering
                Synthetic Genome Editing
                Crispr
                Biology and Life Sciences
                Synthetic Biology
                Synthetic Genomics
                Synthetic Genome Editing
                Crispr
                Engineering and Technology
                Synthetic Biology
                Synthetic Genomics
                Synthetic Genome Editing
                Crispr
                Biology and Life Sciences
                Genetics
                Genomics
                Plant Genomics
                Plant Genomes
                Biology and Life Sciences
                Bioengineering
                Biotechnology
                Plant Biotechnology
                Plant Genomics
                Plant Genomes
                Engineering and Technology
                Bioengineering
                Biotechnology
                Plant Biotechnology
                Plant Genomics
                Plant Genomes
                Biology and Life Sciences
                Plant Science
                Plant Biotechnology
                Plant Genomics
                Plant Genomes
                Biology and Life Sciences
                Genetics
                Plant Genetics
                Plant Genomics
                Plant Genomes
                Biology and Life Sciences
                Plant Science
                Plant Genetics
                Plant Genomics
                Plant Genomes
                Biology and Life Sciences
                Computational Biology
                Genome Analysis
                Sequence Assembly Tools
                Biology and Life Sciences
                Genetics
                Genomics
                Genome Analysis
                Sequence Assembly Tools
                Custom metadata
                All relevant data are within the paper and its Supporting Information files.

                Uncategorized
                Uncategorized

                Comments

                Comment on this article