Evidence map›Paper›PMID 17353263›Full record

ArticleMolecular and cellular biology2007

MEK1 and protein phosphatase 4 coordinate Dictyostelium development and chemotaxis.

Michelle C Mendoza, Ezgi O Booth, Gad Shaulsky, Richard A Firtel

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The principles of directed cell migration.Nature reviews. Molecular cell biology · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Review
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  13. Article
  14. Global transcriptional responses to cisplatin in Dictyostelium discoideum identify potential drug targets.Proceedings of the National Academy of Sciences of the United States of America · 2007
    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

4 authors at 2 institutions in 1 country.

Michelle C MendozaNatural Sciences Building, Room 6316, University of California-San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0380, USA.
Ezgi O Booth
Gad Shaulsky
Richard A Firtel
Baylor College of Medicine · USUniversity of California, San Diego · US

Funding

PROJECT III - Computational Analysis of Phenotypes andP01HD039691 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI SUCGANG, RICHARD · 2001 to 2016
$14.4M
Training Program in Basic Clinical GeneticsT32GM008666 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMILTON, BRUCE A · 1998 to 2021
$8.6M
SIGNALLING PROCESSES IN DICTYOSTELIUMR01GM037830 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRTEL, RICHARD A · 1986 to 2015
$8.5M
Role of Rac and Rac Effectors in Controlling ChemotaxisR01GM062847 · NIGMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI FIRTEL, RICHARD A · 2002 to 2005
$920k
NICHD NIH HHS P01 HD039691NICHD NIH HHS P01 HD 39691NIGMS NIH HHS GM 024727 9NIGMS NIH HHS GM 037830NIGMS NIH HHS GM 062847NIGMS NIH HHS R01 GM037830NIGMS NIH HHS R01 GM062847NIGMS NIH HHS T32 GM008666NIGMS NIH HHS T32 GM 08666-08
6 · The paper itself

Abstract

The MEK and extracellular signal-regulated kinase/mitogen-activated protein kinase proteins are established regulators of multicellular development and cell movement. By combining traditional genetic and biochemical assays with a statistical analysis of global gene expression profiles, we discerned a genetic interaction between Dictyostelium discoideum mek1, smkA (named for its role in the suppression of the mek1(-) mutation), and pppC (the protein phosphatase 4 catalytic subunit gene). We found that during development and chemotaxis, both mek1 and smkA regulate pppC function. In other organisms, the protein phosphatase 4 catalytic subunit, PP4C, functions in a complex with the regulatory subunits PP4R2 and PP4R3 to control recovery from DNA damage. Here, we show that catalytically active PP4C is also required for development, chemotaxis, and the expression of numerous genes. The product of smkA (SMEK) functions as the Dictyostelium PP4R3 homolog and positively regulates a subset of PP4C's functions: PP4C-mediated developmental progression, chemotaxis, and the expression of genes specifically involved in cell stress responses and cell movement. We also demonstrate that SMEK does not control the absolute level of PP4C activity and suggest that SMEK regulates PP4C by controlling its localization to the nucleus. These data define a novel genetic pathway in which mek1 functions upstream of pppC-smkA to control multicellular development and chemotaxis.

Indexed as

AnimalsChemotaxisDictyosteliumEpistasis, GeneticGene Expression ProfilingMAP Kinase Kinase 1Oligonucleotide Array Sequence AnalysisPhosphoprotein PhosphatasesProtein SubunitsProtozoan ProteinsSignal TransductionMAP Kinase Kinase 1Phosphoprotein Phosphatasesprotein phosphatase 4Protein SubunitsProtozoan Proteins

Identifiers

PMID17353263
PMCPMC1899987
OpenAlexW2166378755

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.