Evidence map›Paper›PMID 30847946›Full record

ArticleThe New phytologist2019

RNA-guided endonuclease - in situ labelling (RGEN-ISL): a fast CRISPR/Cas9-based method to label genomic sequences in various species.

Takayoshi Ishii, Veit Schubert, Solmaz Khosravi, Steven Dreissig, Janina Metje-Sprink, Thorben Sprink, Jörg Fuchs, Armin Meister, Andreas Houben

Open access · hybridAbstract read
In one paragraph

Article in The New phytologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. CRISPR-CISH: an in situ chromogenic DNA repeat detection system for research and life science education.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Article
  6. Article
  7. Review
  8. CRISPR-FISH: A CRISPR/Cas9-Based In Situ Labeling Method.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  9. Article
  10. Article
  11. FISH Going Meso-Scale: A Microscopic Search for Chromatin Domains.Frontiers in cell and developmental biology · 2021
    Review
  12. Article
  13. Application and prospects of CRISPR/Cas9-based methods to trace defined genomic sequences in living and fixed plant cells.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2020
    Review
  14. Article
  15. Review
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

9 authors at 2 institutions in 2 countries.

Takayoshi IshiiLeibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Seeland, D-06466, Germany.ORCID 0000-0001-6370-3289
Veit SchubertLeibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Seeland, D-06466, Germany.ORCID 0000-0002-3072-0485
Solmaz KhosraviLeibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Seeland, D-06466, Germany.ORCID 0000-0002-7781-1085
Steven DreissigLeibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Seeland, D-06466, Germany.ORCID 0000-0002-4766-9698
Janina Metje-SprinkJulius Kühn-Institute, Institute of Biosafety in Plant Biotechnology, Quedlinburg, D-06484, Germany.
Thorben SprinkJulius Kühn-Institute, Institute of Biosafety in Plant Biotechnology, Quedlinburg, D-06484, Germany.ORCID 0000-0002-0423-5128
Jörg FuchsLeibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Seeland, D-06466, Germany.ORCID 0000-0003-4171-5371
Armin MeisterLeibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Seeland, D-06466, Germany.
Andreas HoubenLeibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Seeland, D-06466, Germany.ORCID 0000-0003-3419-239X
Leibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK) · DEJulius Kühn-Institut · DE

Funding

CSIRODeutsche Forschungsgemeinschaft Ho1779/28-1
6 · The paper itself

Abstract

Visualising the spatio-temporal organisation of the genome will improve our understanding of how chromatin structure and function are intertwined. We developed a tool to visualise defined genomic sequences in fixed nuclei and chromosomes based on a two-part guide RNA with a recombinant Cas9 endonuclease complex. This method does not require any special construct or transformation method. In contrast to classical fluorescence in situ hybridiaztion, RGEN-ISL (RNA-guided endonuclease - in situ labelling) does not require DNA denaturation, and therefore permits a better structural chromatin preservation. The application of differentially labelled trans-activating crRNAs allows the multiplexing of RGEN-ISL. Moreover, this technique is combinable with immunohistochemistry. Real-time visualisation of the CRISPR/Cas9-mediated DNA labelling process revealed the kinetics of the reaction. The broad range of adaptability of RGEN-ISL to different temperatures and combinations of methods has the potential to advance the field of chromosome biology.

Indexed as

GenomicsStaining and LabelingBase SequenceCentromereCRISPR-Associated Protein 9CRISPR-Cas SystemsEndonucleasesRNA, Guide, CRISPR-Cas SystemsSpecies SpecificityCRISPR-Associated Protein 9EndonucleasesRNA, Guide, CRISPR-Cas SystemscentromereCRISPR/Cas9FISHimmunostainingin situ labellingtelomere

Identifiers

PMID30847946
PMCPMC6593734
OpenAlexW2920913887

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.