Evidence map›Paper›PMID 37936321›Full record

ArticlePlant physiology2024

DOMAIN OF UNKNOWN FUNCTION581-9 negatively regulates SnRK1 kinase activity.

Jennifer Bortlik, Jost Lühle, Saleh Alseekh, Christoph Weiste, Alisdair R Fernie, Wolfgang Dröge-Laser, Frederik Börnke

Open access · hybridAbstract read
In one paragraph

Article in Plant physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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 4 institutions in 2 countries.

Jennifer BortlikPlant Metabolism Group, Department of Plant Adaptation, Leibniz-Institute of Vegetable and Ornamental Crops (IGZ), Großbeeren 14979, Germany.ORCID 0000-0002-1612-8733
Jost LühlePlant Metabolism Group, Department of Plant Adaptation, Leibniz-Institute of Vegetable and Ornamental Crops (IGZ), Großbeeren 14979, Germany.ORCID 0000-0002-1524-5911
Saleh AlseekhDepartment Root Biology and Symbiosis, Max-Planck-Institute of Molecular Plant Physiology, Am Mühlenberg 1, Potsdam-Golm 14476, Germany.ORCID 0000-0003-2067-5235
Christoph WeisteDepartment of Pharmaceutical Biology, Julius-von-Sachs-Institut, Biozentrum, Julius-Maximilians-Universität Würzburg, Würzburg 97082, Germany.ORCID 0000-0003-1894-7924
Alisdair R FernieDepartment Root Biology and Symbiosis, Max-Planck-Institute of Molecular Plant Physiology, Am Mühlenberg 1, Potsdam-Golm 14476, Germany.ORCID 0000-0001-9000-335X
Wolfgang Dröge-LaserCenter for Plant Systems Biology and Biotechnology, Plovdiv 4000, Bulgaria.ORCID 0000-0003-4066-8024
Frederik BörnkePlant Metabolism Group, Department of Plant Adaptation, Leibniz-Institute of Vegetable and Ornamental Crops (IGZ), Großbeeren 14979, Germany.ORCID 0000-0003-3558-0482
Center of Plant Systems Biology and Biotechnology · BGLeibniz Institute of Vegetable and Ornamental Crops · DEUniversity of Potsdam · DEUniversity of Würzburg · DE

Funding

Union's Horizon 2020 Research and Innovation Program 664621
6 · The paper itself

Abstract

In plants, sucrose nonfermenting 1 (SNF1)-related protein kinase 1 (SnRK1) is a key energy sensor that orchestrates large-scale transcriptional reprograming to maintain cellular homeostasis under energy deficit. SnRK1 activity is under tight negative control, although the exact mechanisms leading to its activation are not well understood. We show that the Arabidopsis (Arabidopsis thaliana) DOMAIN OF UNKNOWN FUNCTION (DUF581) protein DUF581-9/FCS-like zinc finger 3 binds to the catalytic SnRK1.1 α subunit (KIN10) to inhibit its activation by geminivirus rep-interacting kinase (GRIK)-dependent T-loop phosphorylation. Overexpression of DUF581-9 in Arabidopsis dampens SnRK1 signaling and interferes with adaptation to dark-induced starvation. The presence of DUF581-9 significantly reduced SnRK1 activity in protoplasts and in vitro. This was accompanied by a reduction in T175 T-loop phosphorylation and also diminished KIN10 auto-phosphorylation. Furthermore, DUF581-9 reduced binding of the upstream activating kinase GRIK2 to KIN10, explaining the reduced KIN10 T-loop phosphorylation. Ectopically expressed DUF581-9 protein was rapidly turned over by the proteasome when Arabidopsis plants were subjected to starvation treatment, likely releasing its inhibitory activity on the SnRK1 complex. Taken together, our results support a model in which DUF581-9 negatively regulates SnRK1 activity under energy sufficient conditions. Turnover of the protein provides a rapid way for SnRK1 activation under energy deficit without the need of de novo protein synthesis.

Indexed as

ArabidopsisArabidopsis ProteinsCatalysisCatalytic DomainCytoplasmPhosphorylationProtein Serine-Threonine KinasesArabidopsis ProteinsAt3g01090 protein, ArabidopsisProtein Serine-Threonine Kinases

Identifiers

PMID37936321
PMCPMC10904321
OpenAlexW4388496232

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.