Evidence map›Paper›PMID 27010942›Full record

ArticlePLoS genetics2016

The DenA/DEN1 Interacting Phosphatase DipA Controls Septa Positioning and Phosphorylation-Dependent Stability of Cytoplasmatic DenA/DEN1 during Fungal Development.

Josua Schinke, Miriam Kolog Gulko, Martin Christmann, Oliver Valerius, Sina Kristin Stumpf, Margarita Stirz, Gerhard H Braus

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. 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
2.1field-weighted citation impact, top 13% 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. Review
  2. Article
  3. Fungal COP9 signalosome assembly requires connection of two trimeric intermediates for integration of intrinsic deneddylase.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  7. HJournal of fungi (Basel, Switzerland) · 2021
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  10. Review
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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

7 authors at 1 institution in 1 country.

Josua SchinkeDepartment of Molecular Microbiology and Genetics, Göttingen Center for Molecular Biosciences (GZMB), and Georg-August-University, Göttingen, Germany.
Miriam Kolog GulkoDepartment of Molecular Microbiology and Genetics, Göttingen Center for Molecular Biosciences (GZMB), and Georg-August-University, Göttingen, Germany.
Martin ChristmannDepartment of Molecular Microbiology and Genetics, Göttingen Center for Molecular Biosciences (GZMB), and Georg-August-University, Göttingen, Germany.
Oliver ValeriusDepartment of Molecular Microbiology and Genetics, Göttingen Center for Molecular Biosciences (GZMB), and Georg-August-University, Göttingen, Germany.
Sina Kristin StumpfDepartment of Molecular Microbiology and Genetics, Göttingen Center for Molecular Biosciences (GZMB), and Georg-August-University, Göttingen, Germany.
Margarita StirzDepartment of Molecular Microbiology and Genetics, Göttingen Center for Molecular Biosciences (GZMB), and Georg-August-University, Göttingen, Germany.
Gerhard H BrausDepartment of Molecular Microbiology and Genetics, Göttingen Center for Molecular Biosciences (GZMB), and Georg-August-University, Göttingen, Germany.
University of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DenA/DEN1 and the COP9 signalosome (CSN) represent two deneddylases which remove the ubiquitin-like Nedd8 from modified target proteins and are required for distinct fungal developmental programmes. The cellular DenA/DEN1 population is divided into a nuclear and a cytoplasmatic subpopulation which is especially enriched at septa. DenA/DEN1 stability control mechanisms are different for the two cellular subpopulations and depend on different physical interacting proteins and the C-terminal DenA/DEN1 phosphorylation pattern. Nuclear DenA/DEN1 is destabilized during fungal development by five of the eight CSN subunits which target nuclear DenA/DEN1 for degradation. DenA/DEN1 becomes stabilized as a phosphoprotein at S243/S245 during vegetative growth, which is necessary to support further asexual development. After the initial phase of development, the newly identified cytoplasmatic DenA/DEN1 interacting phosphatase DipA and an additional developmental specific C-terminal phosphorylation site at serine S253 destabilize DenA/DEN1. Outside of the nucleus, DipA is co-transported with DenA/DEN1 in the cytoplasm between septa and nuclei. Deletion of dipA resulted in increased DenA/DEN1 stability in a strain which is unresponsive to illumination. The mutant strain is dysregulated in cytokinesis and impaired in asexual development. Our results suggest a dual phosphorylation-dependent DenA/DEN1 stability control with stabilizing and destabilizing modifications and physical interaction partner proteins which function as control points in the nucleus and the cytoplasm.

Indexed as

Protein Processing, Post-TranslationalAspergillus nidulansCell NucleusCytokinesisCytoplasmEndopeptidasesEscherichia coliFungal ProteinsGene Expression Regulation, FungalMultiprotein ComplexesPhosphoric Monoester HydrolasesPhosphorylationProtein BindingProtein SubunitsUbiquitinUbiquitinsDEN1 protein, Aspergillus nidulansDipA protein, Aspergillus nidulansEndopeptidasesFungal ProteinsMultiprotein ComplexesPhosphoric Monoester HydrolasesProtein SubunitsUbiquitinUbiquitins

Identifiers

PMID27010942
PMCPMC4806917
OpenAlexW2310985167

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.