Evidence map›Paper›PMID 9742151›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1998

Expression of the mitotic motor protein Eg5 in postmitotic neurons: implications for neuronal development.

L Ferhat, C Cook, M Chauviere, M Harper, M Kress, G E Lyons, P W Baas

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.4field-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

36 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
  2. Review
  3. RSC advances · 2023
    Article
  4. IncreasediScience · 2022
    Article
  5. Article
  6. KIFC1 Regulates the Trajectory of Neuronal Migration.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  7. Review
  8. Review
  9. Mitotic Motor KIFC1 Is an Organizer of Microtubules in the Axon.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  10. Cancer drug therapy and stochastic modeling of "nano-motors".International journal of nanomedicine · 2018
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Ciliobrevins as tools for studying dynein motor function.Frontiers in cellular neuroscience · 2015
    Review
  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

7 authors at 2 institutions in 3 countries.

L FerhatDepartment of Anatomy, The University of Wisconsin Medical School, Madison, Wisconsin 53706, USA.
C Cook
M Chauviere
M Harper
M Kress
G E Lyons
P W Baas
University of Wisconsin–Madison · USLaboratoire d'études sur les monothéismes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well established that the microtubules of the mitotic spindle are organized by a variety of motor proteins, and it appears that the same motors or closely related variants organize microtubules in the postmitotic neuron. Specifically, cytoplasmic dynein and the kinesin-related motor known as CHO1/MKLP1 are used within the mitotic spindle, and recent studies suggest that they are also essential for the establishment of the axonal and dendritic microtubule arrays of the neuron. Other motors are required to tightly regulate microtubule behaviors in the mitotic spindle, and it is attractive to speculate that these motors might also help to regulate microtubule behaviors in the neuron. Here we show that a homolog of the mitotic kinesin-related motor known as Eg5 continues to be expressed in rodent neurons well after their terminal mitotic division. In neurons, Eg5 is directly associated with the microtubule array and is enriched within the distal regions of developing processes. This distal enrichment is transient, and typically lost after a process has been clearly defined as an axon or a dendrite. Strong expression can resume later in development, and if so, the protein concentrates within newly forming sprouts at the distal tips of dendrites. We suggest that Eg5 generates forces that help to regulate microtubule behaviors within the distal tips of developing axons and dendrites.

Indexed as

Xenopus ProteinsAnimalsAxonsBlotting, NorthernCell DifferentiationCloning, MolecularDendritesFluorescent Antibody TechniqueGene ExpressionHippocampusIn Situ HybridizationKinesinsMiceMice, Inbred C3HMicrotubulesMitosisKIF11 protein, XenopusKinesinsRNA, MessengerXenopus Proteins

Identifiers

PMID9742151
PMCPMC6793023
OpenAlexW2121307506

What OpenQuestion holds

Textmetadata
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.