Evidence map›Paper›PMID 18328707›Full record

ArticleCurrent biology : CB2008

Pom1 DYRK regulates localization of the Rga4 GAP to ensure bipolar activation of Cdc42 in fission yeast.

Hisashi Tatebe, Kentaro Nakano, Rachel Maximo, Kazuhiro Shiozaki

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

96 citing papers in PubMed, 189 citations in OpenAlex.

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  11. Patterning of the cell cortex by Rho GTPases.Nature reviews. Molecular cell biology · 2024
    Review
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  20. Genes · 2021
    Review

36 more citing papers are in PubMed but not listed here.

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 2 countries.

Hisashi TatebeSection of Microbiology, College of Biological Sciences, University of California, Davis, California 95616, USA.
Kentaro Nakano
Rachel Maximo
Kazuhiro Shiozaki
University of California, Davis · USUniversity of Tsukuba · JP

Funding

DISSECTION OF STRESS SIGNALING PATHWAYS TO A MAP KINASER01GM059788 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI SHIOZAKI, KAZUHIRO · 1999 to 2011
$3.0M
NIGMS NIH HHS GM59788NIGMS NIH HHS R01 GM059788
6 · The paper itself

Abstract

backgroundIn the fission yeast Schizosaccharomyces pombe, cell growth takes place exclusively at both ends of the cylindrical cell. During this highly polarized growth, microtubules are responsible for the placement of the cell-end marker proteins, the Tea1-Tea4/Wsh3 complex, which recruits the Pom1 DYRK-family protein kinase. Pom1 is required for proper positioning of growth sites, and the Deltapom1 mutation brings about monopolar cell growth.

resultsPom1 kinase physically interacts with Rga4, which has a GAP (GTPase-activating protein) domain for Rho-family GTPase. Genetic and biochemical evidence indicates that Rga4 functions as GAP for the Cdc42 GTPase, an evolutionarily conserved regulator of F-actin. CRIB (Cdc42/Rac interactive binding)-GFP microscopy has revealed that GTP-bound, active Cdc42 is concentrated to growing cell ends accompanied by developed F-actin structures, where the Rga4 GAP is excluded. The monopolar Deltapom1 mutant fails to eliminate Rga4 from the nongrowing cell end, resulting in monopolar distribution of GTP-Cdc42 to the growing cell end. However, mutational inactivation of Rga4 allows Cdc42 to be active at both ends of Deltapom1 cells, suggesting that mislocalization of Rga4 in the Deltapom1 mutant contributes to its monopolar phenotype.

conclusionsPom1 kinase recruited to cell ends by the Tea1-Tea4/Wsh3 complex is essential for proper localization of a GAP for Cdc42, Rga4, which ensures bipolar localization of GTP-bound, active Cdc42. Because of the established role of Cdc42 in F-actin formation, these observations provide a new insight into how the microtubule system achieves localized formation of F-actin to generate cell polarity.

Indexed as

Actinscdc42 GTP-Binding ProteinCell EnlargementCell PolarityCytoskeletonDyrk KinasesGTPase-Activating ProteinsMicrotubulesPhosphorylationProtein KinasesProtein Serine-Threonine KinasesProtein-Tyrosine KinasesSchizosaccharomycesSchizosaccharomyces pombe ProteinsActinscdc42 GTP-Binding ProteinDyrk KinasesGTPase-Activating ProteinsPom1 protein, S pombeProtein KinasesProtein Serine-Threonine KinasesProtein-Tyrosine KinasesRga4 protein, S pombeSchizosaccharomyces pombe Proteins

Identifiers

PMID18328707
PMCPMC2277499
OpenAlexW2101222380

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.