Evidence map›Paper›PMID 12446741›Full record

ArticleThe Journal of cell biology2002

Cytoplasmic linker proteins promote microtubule rescue in vivo.

Yulia A Komarova, Anna S Akhmanova, Shin-Ichiro Kojima, Niels Galjart, Gary G Borisy

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

109 citing papers in PubMed, 245 citations in OpenAlex.

  1. Article
  2. CLASP2 promotes repair of kinesin-1 damage to the microtubule lattice.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
  5. Autophagy initiation triggers p150Cellular and molecular life sciences : CMLS · 2024
    Article
  6. Article
  7. Phase separation of +TIP networks regulates microtubule dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Article
  9. Article
  10. Microtubule detyrosination drives symmetry breaking to polarize cells for directed cell migration.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  11. Review
  12. Article
  13. Article
  14. Persistent growth of microtubules at low density.Molecular biology of the cell · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Microtubules in cell migration.Essays in biochemistry · 2019
    Review

49 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Yulia A KomarovaDepartment of Cell and Molecular Biology, N University Medical School, Chicago, IL 60611, USA. y-komarova@northwestern.edu
Anna S Akhmanova
Shin-Ichiro Kojima
Niels Galjart
Gary G Borisy
Northwestern University · USErasmus University Rotterdam · NL

Funding

MECHANISM AND CONTROL OF MICROTUBULE ASSEMBLYR01GM025062 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI BORISY, GARY G · 1985 to 2003
$1.9M
MECHANISM AND CONTROL OF MICROTUBULE ASSEMBLYR37GM025062 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI BORISY, GARY G · 1989 to 1998
–
NIGMS NIH HHS GM 25062NIGMS NIH HHS R01 GM025062NIGMS NIH HHS R37 GM025062
6 · The paper itself

Abstract

The role of plus end-tracking proteins in regulating microtubule (MT) dynamics was investigated by expressing a dominant negative mutant that removed endogenous cytoplasmic linker proteins (CLIPs) from MT plus ends. In control CHO cells, MTs exhibited asymmetric behavior: MTs persistently grew toward the plasma membrane and displayed frequent fluctuations of length near the cell periphery. In the absence of CLIPs, the microtubule rescue frequency was reduced by sevenfold. MT behavior became symmetrical, consisting of persistent growth and persistent shortening. Removal of CLIPs also caused loss of p150Glued but not CLIP-associating protein (CLASP2) or EB1. This result raised the possibility that the change in dynamics was a result of the loss of either CLIPs or p150Glued. To distinguish between these possibilities, we performed rescue experiments. Normal MT dynamics were restored by expression of the CLIP-170 head domain, but p150Glued was not recruited back to MT plus ends. Expression of p150Glued head domain only partially restored MT dynamics. We conclude that the CLIP head domain is sufficient to alter MT dynamics either by itself serving as a rescue factor or indirectly by recruiting a rescue factor. By promoting a high rescue frequency, CLIPs provide a mechanism by which MT plus ends may be concentrated near the cell margin.

Indexed as

AnimalsCHO CellsCOS CellsCricetinaeDynactin ComplexHumansMicrotubule-Associated ProteinsMicrotubulesNeoplasm ProteinsRatsRecombinant Fusion Proteinscytoplasmic linker protein 170Dynactin ComplexEB1 microtubule binding proteinsMicrotubule-Associated ProteinsNeoplasm ProteinsRecombinant Fusion Proteins

Identifiers

PMID12446741
PMCPMC2173097
OpenAlexW2021135236

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.