Evidence map›Paper›PMID 9168476›Full record

ArticleMolecular biology of the cell1997

Role of Dictyostelium racE in cytokinesis: mutational analysis and localization studies by use of green fluorescent protein.

D A Larochelle, K K Vithalani, A De Lozanne

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.2field-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

30 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Functional integrity of the contractile actin cortex is safeguarded by multiple Diaphanous-related formins.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  6. Article
  7. Article
  8. Rho GTPases orient directional sensing in chemotaxis.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  9. Cytokinesis through biochemical-mechanical feedback loops.Seminars in cell & developmental biology · 2010
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Balance of actively generated contractile and resistive forces controls cytokinesis dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  15. Article
  16. Article
  17. Signal transduction pathways regulated by Rho GTPases in Dictyostelium.Journal of muscle research and cell motility · 2002
    Review
  18. Dictyostelium cytokinesis: from molecules to mechanics.Journal of muscle research and cell motility · 2002
    Review
  19. Article
  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

3 authors at 1 institution in 1 country.

D A LarochelleDepartment of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.
K K Vithalani
A De Lozanne
Duke University · US

Funding

MOLECULAR ANALYSIS OF CYTOKINESIS IN DICTYOSTELIUMR01GM048745 · NIGMS · UNIVERSITY OF TEXAS AUSTIN · PI DE LOZANNE, ARTURO · 1998 to 2006
$1.9M
MOLECULAR ANALYSIS OF CYTOKINESIS IN DICTYOSTELIUMR29GM048745 · NIGMS · DUKE UNIVERSITY · PI DE LOZANNE, ARTURO · 1993 to 1997
–
NIGMS NIH HHS GM 48745
6 · The paper itself

Abstract

The small GTPase racE is essential for cytokinesis in Dictyostelium but its precise role in cell division is not known. To determine the molecular mechanism of racE function, we undertook a mutational analysis of racE. The exogenous expression of either wild-type racE or a constitutively active V20racE mutant effectively rescues the cytokinesis deficiency of racE null cells. In contrast, a constitutively inactive N25racE mutant fails to rescue the cytokinesis deficiency. Thus, cytokinesis requires only the activation of racE by GTP and not the inactivation of racE by hydrolysis of GTP. To determine the spatial distribution of racE, we created a fusion protein with GFP at the amino terminus of racE. Remarkably, GFP-racE fusion protein was fully competent to rescue the phenotype of racE null cells and, therefore, must reside in the same location as native racE. We found that GFP-racE localized to the plasma membrane of the cell throughout the entire cell cycle. Furthermore, constitutively active and inactive GFP-racE fusion proteins also localized to the plasma membrane. We mapped the domain required for plasma membrane localization to the carboxyl-terminal 40 amino acids of racE. This domain, however, is not sufficient to confer racE function onto a closely related GTPase. Taken together, these results suggest that racE functions at the cell cortex but it is not involved in determining the timing or placement of the contractile ring.

Indexed as

rac GTP-Binding ProteinsAnimalsCell DivisionCell MembraneDictyosteliumEnzyme ActivationGene ExpressionGreen Fluorescent ProteinsGTP-Binding ProteinsLuminescent ProteinsPhenotypeRecombinant Fusion ProteinsGreen Fluorescent ProteinsGTP-Binding ProteinsLuminescent ProteinsRacE protein, Dictyostelium discoideumrac GTP-Binding ProteinsRecombinant Fusion Proteins

Identifiers

PMID9168476
PMCPMC276139
OpenAlexW2096945586

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.