Evidence map›Paper›PMID 30787279›Full record

ArticleNature communications2019

The companion of cellulose synthase 1 confers salt tolerance through a Tau-like mechanism in plants.

Christopher Kesten, Arndt Wallmann, René Schneider, Heather E McFarlane, Anne Diehl, Ghazanfar Abbas Khan, Barth-Jan van Rossum, Edwin R Lampugnani, Witold G Szymanski, Nils Cremer and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
16.6field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 96 citations in OpenAlex.

  1. Abiotic Stress in Crop Production.International journal of molecular sciences · 2023
    Pooled it
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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

17 authors at 4 institutions in 3 countries.

Christopher KestenDepartment of Biology, ETH Zurich, 8092, Zurich, Switzerland.
Arndt WallmannLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), NMR-supported Structural Biology, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
René SchneiderSchool of Biosciences, University of Melbourne, Parkville, 3010, Victoria, Australia.
Heather E McFarlaneSchool of Biosciences, University of Melbourne, Parkville, 3010, Victoria, Australia.
Anne DiehlLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), NMR-supported Structural Biology, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
Ghazanfar Abbas KhanSchool of Biosciences, University of Melbourne, Parkville, 3010, Victoria, Australia.
Barth-Jan van RossumLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), NMR-supported Structural Biology, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
Edwin R LampugnaniSchool of Biosciences, University of Melbourne, Parkville, 3010, Victoria, Australia.
Witold G SzymanskiMax-Planck-Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam-Golm, Germany.
Nils CremerLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), NMR-supported Structural Biology, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
Peter SchmiederLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), NMR-supported Structural Biology, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
Kristina L FordSchool of Biosciences, University of Melbourne, Parkville, 3010, Victoria, Australia.
Florian SeiterLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), NMR-supported Structural Biology, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
Joshua L HeazlewoodSchool of Biosciences, University of Melbourne, Parkville, 3010, Victoria, Australia.
Clara Sanchez-RodriguezDepartment of Biology, ETH Zurich, 8092, Zurich, Switzerland.
Hartmut OschkinatLeibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), NMR-supported Structural Biology, Robert-Rössle-Str. 10, 13125, Berlin, Germany. oschkinat@fmp-berlin.de.
Staffan PerssonSchool of Biosciences, University of Melbourne, Parkville, 3010, Victoria, Australia. Staffan.persson@unimelb.edu.au.
Leibniz-Forschungsinstitut für Molekulare Pharmakologie · DEUniversity of Melbourne · AUMax Planck Institute of Molecular Plant Physiology · DEETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microtubules are filamentous structures necessary for cell division, motility and morphology, with dynamics critically regulated by microtubule-associated proteins (MAPs). Here we outline the molecular mechanism by which the MAP, COMPANION OF CELLULOSE SYNTHASE1 (CC1), controls microtubule bundling and dynamics to sustain plant growth under salt stress. CC1 contains an intrinsically disordered N-terminus that links microtubules at evenly distributed points through four conserved hydrophobic regions. By NMR and live cell analyses we reveal that two neighboring residues in the first hydrophobic binding motif are crucial for the microtubule interaction. The microtubule-binding mechanism of CC1 is reminiscent to that of the prominent neuropathology-related protein Tau, indicating evolutionary convergence of MAP functions across animal and plant cells.

Indexed as

ArabidopsisArabidopsis ProteinsCelluloseGlucosyltransferasesHydrophobic and Hydrophilic InteractionsMicrotubule-Associated ProteinsMicrotubulesSalt ToleranceSeedlingstau ProteinsArabidopsis ProteinsCC1 protein, ArabidopsisCellulosecellulose synthaseGlucosyltransferasesMicrotubule-Associated Proteinstau Proteins

Identifiers

PMID30787279
PMCPMC6382854
OpenAlexW2917111827

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.