Evidence map›Paper›PMID 12796292›Full record

ArticleEukaryotic cell2003

RacB regulates cytoskeletal function in Dictyostelium spp.

Eunkyung Lee, David J Seastone, Ed Harris, James A Cardelli, David A Knecht

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Convergence of Ras- and Rac-regulated formin pathways is pivotal for phagosome formation and particle uptake inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  3. Article
  4. Review
  5. Function of small GTPases in Dictyostelium macropinocytosis.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Review
  6. Article
  7. Article
  8. Involvement of Membrane Blebbing in Immunological Disorders and Cancer.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2016
    Review
  9. Article
  10. Cell motility through plasma membrane blebbing.The Journal of cell biology · 2008
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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 at 3 institutions in 1 country.

Eunkyung LeeDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut 06269, USA.
David J Seastone
Ed Harris
James A Cardelli
David A Knecht
Louisiana State University · USUniversity Hospital and Clinics · USUniversity Medical Center · US

Funding

Molecular Genetics of the CytoskeletonR01GM040599 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI KNECHT, DAVID A · 1988 to 2009
$1.8M
TARGETING OF LYSOSOMAL ENZYMES IN DICTYOSTELIUMR01DK039232 · NIDDK · LOUISIANA STATE UNIV HSC SHREVEPORT · PI CARDELLI, JAMES · 1992 to 2001
$365k
TARGETING O LYSOSOMAL ENZYMES IN DICTYOSTELIUM DISCOIDEUR29DK039232 · NIDDK · LOUISIANA STATE UNIV HSC SHREVEPORT · PI CARDELLI, JAMES · 1988 to 1990
–
NIDDK NIH HHS DK 39232NIGMS NIH HHS GM40599NIGMS NIH HHS R01 GM040599
6 · The paper itself

Abstract

Thus far, 14 homologues of mammalian Rac proteins have been identified in Dictyostelium. It is unclear whether each of these genes has a unique function or to what extent they play redundant roles in actin cytoskeletal organization. To investigate the specific function of RacB, we have conditionally expressed wild-type (WT-RacB), dominant negative (N17-RacB), and constitutively activated (V12-RacB) versions of the protein. On induction, cells expressing V12-RacB stopped growing, detached from the surface, and formed numerous spherical surface protrusions while cells overexpressing WT-RacB became flattened on the surface. In contrast, cells overexpressing N17-RacB did not show any significant morphological abnormalities. The surface protrusions seen in V12-RacB cells appear to be actin-driven protrusions because they were enriched in F-actin and were inhibitable by cytochalasin A treatment. The protrusions in V12-RacB cells did not require myosin II activity, which distinguishes them from blebs formed by wild-type cells under stress. Finally, we examined the functional consequences of expression of wild-type and mutant RacB. Phagocytosis, endocytosis, and fluid phase efflux rates were reduced in all cell lines expressing RacB proteins but the greatest decrease was observed for cells expressing V12-RacB. From these results, we conclude that like other members of the Rho family, RacB induces polymerization of actin but the consequences of activation appear to be different from other Dictyostelium Rac proteins so far investigated, resulting in different morphological and functional changes in cells.

Indexed as

ActinsAnimalsCells, CulturedCytochalasinsCytoskeletonDictyosteliumMutagenesisOximesPseudopodiarac GTP-Binding ProteinsTransformation, GeneticActinscytochalasin ACytochalasinsOximesrac GTP-Binding Proteins

Identifiers

PMID12796292
PMCPMC161455
OpenAlexW2170959283

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.