Evidence map›Paper›PMID 15657426›Full record

ArticleMolecular and cellular biology2005

Regulation of Rho and Rac signaling to the actin cytoskeleton by paxillin during Drosophila development.

Guang-Chao Chen, Brian Turano, Paul J Ruest, Margit Hagel, Jeffrey Settleman, Sheila M Thomas

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 65 citations in OpenAlex.

  1. Decoding Rho GTPase signalling networks in directed cell migration.Frontiers in cell and developmental biology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Epithelial morphogenesis in theFrontiers in cell and developmental biology · 2022
    Article
  8. Article
  9. Article
  10. Paxillin: a crossroad in pathological cell migration.Journal of hematology & oncology · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
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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

6 authors at 3 institutions in 1 country.

Guang-Chao ChenMassachusetts General Hospital Cancer Center and Harvard Medical School, 149 13th Street, Charlestown, MA 02129, USA.
Brian Turano
Paul J Ruest
Margit Hagel
Jeffrey Settleman
Sheila M Thomas
Harvard University · USBeth Israel Deaconess Medical Center · USMassachusetts General Hospital · US

Funding

RHO GTPASE SIGNALING IN EMBRYO MORPHOGENESISR01GM060466 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI SETTLEMAN, JEFFREY E · 2000 to 2003
$1.1M
SIGNALING THROUGH THE CYTOSKELETAL PROTEIN, PAXILLINR01CA075621 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI THOMAS, SHEILA M · 1997 to 2001
$520k
NCI NIH HHS R01 CA 75621NIGMS NIH HHS R01 GM060466NIGMS NIH HHS R01 GM 60466
6 · The paper itself

Abstract

Paxillin is a prominent focal adhesion docking protein that regulates cell adhesion and migration. Although numerous paxillin-binding proteins have been identified and paxillin is required for normal embryogenesis, the precise mechanism by which paxillin functions in vivo has not yet been determined. We identified an ortholog of mammalian paxillin in Drosophila (Dpax) and have undertaken a genetic analysis of paxillin function during development. Overexpression of Dpax disrupted leg and wing development, suggesting a role for paxillin in imaginal disc morphogenesis. These defects may reflect a function for paxillin in regulation of Rho family GTPase signaling as paxillin interacts genetically with Rac and Rho in the developing eye. Moreover, a gain-of-function suppressor screen identified a genetic interaction between Dpax and cdi in wing development. cdi belongs to the cofilin kinase family, which includes the downstream Rho target, LIM kinase (LIMK). Significantly, strong genetic interactions were detected between Dpax and Dlimk, as well as downstream effectors of Dlimk. Supporting these genetic data, biochemical studies indicate that paxillin regulates Rac and Rho activity, positively regulating Rac and negatively regulating Rho. Taken together, these data indicate the importance of paxillin modulation of Rho family GTPases during development and identify the LIMK pathway as a critical target of paxillin-mediated Rho regulation.

Indexed as

Actin Depolymerizing FactorsActinsAmino Acid SequenceAnimalsCytoskeletal ProteinsCytoskeletonDrosophilaDrosophila ProteinsEmbryo, NonmammalianLim KinasesMicrofilament ProteinsMolecular Sequence DataPaxillinPhosphoproteinsProtein Kinasesrac GTP-Binding ProteinsActin Depolymerizing FactorsActinsCytoskeletal ProteinsDrosophila ProteinsLim KinasesMicrofilament ProteinsPaxillinPax protein, DrosophilaPhosphoproteinsProtein Kinasesrac GTP-Binding Proteinsrho GTP-Binding Proteins

Identifiers

PMID15657426
PMCPMC544021
OpenAlexW2170984431

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.