Evidence map›Paper›PMID 30568723›Full record

ArticlePlant methods2018

A simple and efficient CRISPR/Cas9 platform for induction of single and multiple, heritable mutations in barley (

Sebastian Gasparis, Maciej Kała, Mateusz Przyborowski, Leszek A Łyżnik, Wacław Orczyk, Anna Nadolska-Orczyk

Abstract read
In one paragraph

Article in Plant methods, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed.

  1. Article
  2. Article
  3. Rapid development of naked malting barley germplasm through targeted mutagenesis.Molecular breeding : new strategies in plant improvement · 2025
    Article
  4. Beyond a few bases: methods for large DNA insertion and gene targeting in plants.The Plant journal : for cell and molecular biology · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. International journal of molecular sciences · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. CRISPR-Cas technology a new era in genomic engineering.Biotechnology reports (Amsterdam, Netherlands) · 2022
    Review
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sebastian Gasparis1Department of Functional Genomics, Plant Breeding and Acclimatization Institute - National Research Institute, 05-870 Radzików, Błonie, Poland.ORCID 0000-0003-0521-086X
Maciej Kała1Department of Functional Genomics, Plant Breeding and Acclimatization Institute - National Research Institute, 05-870 Radzików, Błonie, Poland.
Mateusz Przyborowski1Department of Functional Genomics, Plant Breeding and Acclimatization Institute - National Research Institute, 05-870 Radzików, Błonie, Poland.
Leszek A Łyżnik2Department of Plant Genetics, Breeding and Biotechnology, Warsaw University of Life Sciences (SGGW), 02-776 Warsaw, Poland.
Wacław Orczyk3Department of Genetic Engineering, Plant Breeding and Acclimatization Institute - National Research Institute, 05-870 Radzików, Błonie, Poland.
Anna Nadolska-Orczyk1Department of Functional Genomics, Plant Breeding and Acclimatization Institute - National Research Institute, 05-870 Radzików, Błonie, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenome editing of monocot plants can be accomplished by using the components of the CRISPR/Cas9 (clustered regularly interspaced short palindromic repeat/CRISPR associated Cas9) technology specifically optimized for these types of plants. Here, we present the development of RNA-guided Cas9 system for simplex and multiplex genome editing in barley.

resultsWe developed a set of customizable RNA-guided Cas9 binary vectors and sgRNA modules for simplex and multiplex editing in barley. To facilitate the design of RNA-guided Cas9 constructs, the pBract derived binary vectors were adapted to Gateway cloning and only one restriction enzyme was required for construction of the sgRNA. We designed a synthetic, codon optimized Cas9 gene containing the N terminal SV40 nuclear localization signal and the UBQ10

conclusionsWe demonstrated the effectiveness of an optimized RNA-guided Cas9 system that can be used for generating homozygous knockout mutants in the progeny of transgenic barely plants. This is also the first report of successful multiplex editing in barley using a tRNA processing system.

Indexed as

BarleyCKX genesCRISPR/Cas9Genome editingPTG

Identifiers

PMID30568723
PMCPMC6297969

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.