Evidence map›Paper›PMID 19536333›Full record

ArticlePloS one2009

Actin turnover is required for myosin-dependent mitochondrial movements in Arabidopsis root hairs.

Maozhong Zheng, Martina Beck, Jens Müller, Tong Chen, Xiaohua Wang, Feng Wang, Qinli Wang, Yuqing Wang, Frantisek Baluska, David C Logan and 2 more

Abstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

30 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Visualizing the dynamics of plant energy organelles.Biochemical Society transactions · 2023
    Article
  7. Article
  8. Plants (Basel, Switzerland) · 2023
    Article
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  11. Article
  12. Article
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4 · The record

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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

12 authors.

Maozhong ZhengKey Laboratory of Photosynthesis and Molecular Environmental Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing, China.
Martina Beck
Jens Müller
Tong Chen
Xiaohua Wang
Feng Wang
Qinli Wang
Yuqing Wang
Frantisek Baluska
David C Logan
Jozef Samaj
Jinxing Lin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies have shown that plant mitochondrial movements are myosin-based along actin filaments, which undergo continuous turnover by the exchange of actin subunits from existing filaments. Although earlier studies revealed that actin filament dynamics are essential for many functions of the actin cytoskeleton, there are little data connecting actin dynamics and mitochondrial movements. METHODOLOGY/PRINCIPAL

findingsWe addressed the role of actin filament dynamics in the control of mitochondrial movements by treating cells with various pharmaceuticals that affect actin filament assembly and disassembly. Confocal microscopy of Arabidopsis thaliana root hairs expressing GFP-FABD2 as an actin filament reporter showed that mitochondrial distribution was in agreement with the arrangement of actin filaments in root hairs at different developmental stages. Analyses of mitochondrial trajectories and instantaneous velocities immediately following pharmacological perturbation of the cytoskeleton using variable-angle evanescent wave microscopy and/or spinning disk confocal microscopy revealed that mitochondrial velocities were regulated by myosin activity and actin filament dynamics. Furthermore, simultaneous visualization of mitochondria and actin filaments suggested that mitochondrial positioning might involve depolymerization of actin filaments on the surface of mitochondria. CONCLUSIONS/SIGNIFICANCE: Base on these results we propose a mechanism for the regulation of mitochondrial speed of movements, positioning, and direction of movements that combines the coordinated activity of myosin and the rate of actin turnover, together with microtubule dynamics, which directs the positioning of actin polymerization events.

Indexed as

Actin CytoskeletonActinsArabidopsisArabidopsis ProteinsCytoskeletonGreen Fluorescent ProteinsMicroscopy, ConfocalMicrotubulesMitochondriaModels, BiologicalModels, StatisticalMyosinsPlant RootsPlasmidsActinsArabidopsis ProteinsGreen Fluorescent ProteinsMyosins

Identifiers

PMID19536333
PMCPMC2694364

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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.