Evidence map›Paper›PMID 20375144›Full record

ArticleMolecular biology of the cell2010

Involvement of the cytoskeleton in controlling leading-edge function during chemotaxis.

Susan Lee, Zhouxin Shen, Douglas N Robinson, Steven Briggs, Richard A Firtel

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Article
  2. Queue Gaps Among the IQGAPs inInternational journal of molecular sciences · 2026
    Review
  3. Review
  4. Article
  5. Signaling and actin waves at a glance.Journal of cell science · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Microtopographical guidance of macropinocytic signaling patches.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Article
  13. Review
  14. IQGAP-related protein IqgC suppresses Ras signaling during large-scale endocytosis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Article
  16. 14-3-3 proteins tune non-muscle myosin II assembly.The Journal of biological chemistry · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. Novel protein Callipygian defines the back of migrating cells.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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.

Susan LeeDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093-0380, USA.
Zhouxin Shen
Douglas N Robinson
Steven Briggs
Richard A Firtel

Funding

SIGNALLING PROCESSES IN DICTYOSTELIUMR01GM037830 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRTEL, RICHARD A · 1986 to 2015
$8.5M
The Biochemical Basis for the Mechanics of CytokinesisR01GM066817 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ROBINSON, DOUGLAS N · 2003 to 2025
$7.3M
Quantitative Analysis of Chemotactic Motility Cycle of Ameboid CellsR01GM084227 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEL ALAMO, JUAN CARLOS, FIRTEL, RICHARD A · 2010 to 2018
$2.7M
NIGMS NIH HHS GM066817NIGMS NIH HHS R01 GM037830NIGMS NIH HHS R01 GM066817NIGMS NIH HHS R01 GM084227
6 · The paper itself

Abstract

In response to directional stimulation by a chemoattractant, cells rapidly activate a series of signaling pathways at the site closest to the chemoattractant source that leads to F-actin polymerization, pseudopod formation, and directional movement up the gradient. Ras proteins are major regulators of chemotaxis in Dictyostelium; they are activated at the leading edge, are required for chemoattractant-mediated activation of PI3K and TORC2, and are one of the most rapid responders, with activity peaking at approximately 3 s after stimulation. We demonstrate that in myosin II (MyoII) null cells, Ras activation is highly extended and is not restricted to the site closest to the chemoattractant source. This causes elevated, extended, and spatially misregulated activation of PI3K and TORC2 and their effectors Akt/PKB and PKBR1, as well as elevated F-actin polymerization. We further demonstrate that disruption of specific IQGAP/cortexillin complexes, which also regulate cortical mechanics, causes extended activation of PI3K and Akt/PKB but not Ras activation. Our findings suggest that MyoII and IQGAP/cortexillin play key roles in spatially and temporally regulating leading-edge activity and, through this, the ability of cells to restrict the site of pseudopod formation.

Indexed as

AnimalsChemotaxisCyclic AMPCytoskeletonDictyosteliumMicrofilament ProteinsMyosin Type IIPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProtozoan ProteinsPseudopodiarac1 GTP-Binding Proteinras GTPase-Activating Proteinsras ProteinsRecombinant Fusion ProteinsSignal TransductionctxA protein, Dictyostelium discoideumctxB protein, Dictyostelium discoideumCyclic AMPIQ motif containing GTPase activating protein 1Microfilament ProteinsMyosin Type IIPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProtozoan Proteinsrac1 GTP-Binding Proteinras GTPase-Activating Proteinsras ProteinsRecombinant Fusion Proteins

Identifiers

PMID20375144
PMCPMC2877640

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.