Evidence map›Paper›PMID 27811079›Full record

ArticleJournal of experimental botany2016

Visualization of specific repetitive genomic sequences with fluorescent TALEs in Arabidopsis thaliana.

Satoru Fujimoto, Shigeo S Sugano, Keiko Kuwata, Keishi Osakabe, Sachihiro Matsunaga

Open access · hybridAbstract read
In one paragraph

Article in Journal of experimental botany, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
12.3field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  7. Review
  8. Article
  9. 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
  10. Kleptoprotein bioluminescence:Science advances · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Fluorescence in situ hybridization in plants: recent developments and future applications.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2019
    Review
  15. Article
  16. Article
  17. Live-cell CRISPR imaging in plants reveals dynamic telomere movements.The Plant journal : for cell and molecular biology · 2017
    Article
  18. Article
  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

5 authors at 4 institutions in 1 country.

Satoru FujimotoDepartment of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Shigeo S SuganoGraduate School of Science, Kyoto University, Kyoto 606-8502, Japan.
Keiko KuwataInstitute of Transformative Bio-Molecules, Nagoya University, Nagoya 464-8601, Japan.
Keishi OsakabeFaculty of Bioscience and Bioindustry, Tokushima University, Tokushima 770-8513, Japan.
Sachihiro MatsunagaDepartment of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Noda, Chiba 278-8510, Japan sachi@rs.tus.ac.jp.
Tokyo University of Science · JPKyoto University · JPNagoya University · JPTokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Live imaging of the dynamics of nuclear organization provides the opportunity to uncover the mechanisms responsible for four-dimensional genome architecture. Here, we describe the use of fluorescent protein (FP) fusions of transcription activator-like effectors (TALEs) to visualize endogenous genomic sequences in Arabidopsis thaliana. The ability to engineer sequence-specific TALEs permits the investigation of precise genomic sequences. We could detect TALE-FP signals associated with centromeric, telomeric, and rDNA repeats and the signal distribution was consistent with that observed by fluorescent in situ hybridization. TALE-FPs are advantageous because they permit the observation of intact tissues. We used our TALE-FP method to investigate the nuclei of several multicellular plant tissues including roots, hypocotyls, leaves, and flowers. Because TALE-FPs permit live-cell imaging, we successfully observed the temporal dynamics of centromeres and telomeres in plant organs. Fusing TALEs to multimeric FPs enhanced the signal intensity when observing telomeres. We found that the mobility of telomeres was different in sub-nuclear regions. Transgenic plants stably expressing TALE-FPs will provide new insights into chromatin organization and dynamics in multicellular organisms.

Indexed as

ArabidopsisGenome, PlantGreen Fluorescent ProteinsImmunoprecipitationIn Situ Hybridization, FluorescenceRepetitive Sequences, Nucleic AcidTranscription Activator-Like EffectorsGreen Fluorescent ProteinsTranscription Activator-Like EffectorsCentromerechromatinfluorescent proteingenome editinglive cell imagingrDNAtelomeretranscription activator-like effector.

Identifiers

PMID27811079
PMCPMC5100022
OpenAlexW2529352483

What OpenQuestion holds

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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.