Evidence map›Paper›PMID 33674706›Full record

ArticleCommunications biology2021

Mitochondrial movement during its association with chloroplasts in Arabidopsis thaliana.

Kazusato Oikawa, Takuto Imai, Chonprakun Thagun, Kiminori Toyooka, Takeshi Yoshizumi, Kazuya Ishikawa, Yutaka Kodama, Keiji Numata

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
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  7. Review
  8. Plastid Transient and Stable Interactions with Other Cell Compartments.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  9. Visualizing the dynamics of plant energy organelles.Biochemical Society transactions · 2023
    Article
  10. Mitochondrial signal transduction.Cell metabolism · 2022
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. 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

8 authors at 3 institutions in 1 country.

Kazusato OikawaDepartment of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan.
Takuto ImaiBiomacromolecules Research Team, RIKEN Center for Sustainable Resource Science, Saitama, Japan.
Chonprakun ThagunBiomacromolecules Research Team, RIKEN Center for Sustainable Resource Science, Saitama, Japan.
Kiminori ToyookaMass Spectrometry and Microscopy Unit, RIKEN Center for Sustainable Resource Science, Yokohama, Japan.ORCID 0000-0002-6414-5191
Takeshi YoshizumiBiomacromolecules Research Team, RIKEN Center for Sustainable Resource Science, Saitama, Japan.
Kazuya IshikawaCenter for Bioscience Research and Education, Utsunomiya University, Utsunomiya, Japan.
Yutaka KodamaBiomacromolecules Research Team, RIKEN Center for Sustainable Resource Science, Saitama, Japan. kodama@cc.utsunomiya-u.ac.jp.ORCID 0000-0002-4720-7311
Keiji NumataDepartment of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan. keiji.numata@riken.jp.ORCID 0000-0003-2199-7420
RIKEN Center for Sustainable Resource Science · JPKyoto University · JPUtsunomiya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant mitochondria move dynamically inside cells and this movement is classified into two types: directional movement, in which mitochondria travel long distances, and wiggling, in which mitochondria travel short distances. However, the underlying mechanisms and roles of both types of mitochondrial movement, especially wiggling, remain to be determined. Here, we used confocal laser-scanning microscopy to quantitatively characterize mitochondrial movement (rate and trajectory) in Arabidopsis thaliana mesophyll cells. Directional movement leading to long-distance migration occurred at high speed with a low angle-change rate, whereas wiggling leading to short-distance migration occurred at low speed with a high angle-change rate. The mean square displacement (MSD) analysis could separate these two movements. Directional movement was dependent on filamentous actin (F-actin), whereas mitochondrial wiggling was not, but slightly influenced by F-actin. In mesophyll cells, mitochondria could migrate by wiggling, and most of these mitochondria associated with chloroplasts. Thus, mitochondria migrate via F-actin-independent wiggling under the influence of F-actin during their association with chloroplasts in Arabidopsis.

Indexed as

MovementActin CytoskeletonActinsArabidopsisChloroplast Proton-Translocating ATPasesChloroplastsLuminescent ProteinsMesophyll CellsMicroscopy, ConfocalMicroscopy, VideoMitochondriaPlants, Genetically ModifiedRecombinant Fusion ProteinsTime FactorsTime-Lapse ImagingActinsChloroplast Proton-Translocating ATPasesLuminescent ProteinsRecombinant Fusion Proteins

Identifiers

PMID33674706
PMCPMC7935954
OpenAlexW3134635185

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.