Evidence map›Paper›PMID 19509299›Full record

ArticleThe Journal of biological chemistry2009

Heteromeric AtKC1{middle dot}AKT1 channels in Arabidopsis roots facilitate growth under K+-limiting conditions.

Dietmar Geiger, Dirk Becker, Daniel Vosloh, Franco Gambale, Klaus Palme, Marion Rehers, Uta Anschuetz, Ingo Dreyer, Jörg Kudla, Rainer Hedrich

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
17.7field-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

63 citing papers in PubMed, 175 citations in OpenAlex.

  1. A Salt-ResponsiveInternational journal of molecular sciences · 2026
    Article
  2. Article
  3. Article
  4. The Potassium Utilization Gene Network inInternational journal of molecular sciences · 2025
    Article
  5. Review
  6. Arabidopsis HAK5 under low KNature communications · 2024
    Article
  7. Research Progress on Plant Shaker KPlants (Basel, Switzerland) · 2024
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Identification and Characterization of Shaker KFrontiers in plant science · 2022
    Article
  14. Article
  15. Sugar perception in honeybees.Frontiers in physiology · 2022
    Article
  16. Review
  17. Adjustment of KInternational journal of molecular sciences · 2021
    Review
  18. Article
  19. Article
  20. Article

3 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

10 authors at 5 institutions in 5 countries.

Dietmar GeigerJulius-von-Sachs-Institute, Molecular Plant Physiology and Biophysics, University of Wuerzburg, Julius-von-Sachs-Platz 2, D-97082 Wuerzburg, Germany.
Dirk Becker
Daniel Vosloh
Franco Gambale
Klaus Palme
Marion Rehers
Uta Anschuetz
Ingo Dreyer
Jörg Kudla
Rainer Hedrich
Leibniz Association · DEInstitute of Botany · AZInstitute of Plant Biology and Biotechnology · KZInstituto Biofisika · ESUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant growth and development is driven by osmotic processes. Potassium represents the major osmotically active cation in plants cells. The uptake of this inorganic osmolyte from the soil in Arabidopsis involves a root K(+) uptake module consisting of the two K(+) channel alpha-subunits, AKT1 and AtKC1. AKT1-mediated potassium absorption from K(+)-depleted soil was shown to depend on the calcium-sensing proteins CBL1/9 and their interacting kinase CIPK23. Here we show that upon activation by the CBL.CIPK complex in low external potassium homomeric AKT1 channels open at voltages positive of E(K), a condition resulting in cellular K(+) leakage. Although at submillimolar external potassium an intrinsic K(+) sensor reduces AKT1 channel cord conductance, loss of cytosolic potassium is not completely abolished under these conditions. Depending on channel activity and the actual potassium gradients, this channel-mediated K(+) loss results in impaired plant growth in the atkc1 mutant. Incorporation of the AtKC1 subunit into the channel complex, however, modulates the properties of the K(+) uptake module to prevent K(+) loss. Upon assembly of AKT1 and AtKC1, the activation threshold of the root inward rectifier voltage gate is shifted negative by approximately -70 mV. Additionally, the channel conductance gains a hypersensitive K(+) dependence. Together, these two processes appear to represent a safety strategy preventing K(+) loss through the uptake channels under physiological conditions. Similar growth retardation phenotypes of akt1 and atkc1 loss-of-function mutants in response to limiting K(+) supply further support such functional interdependence of AKT1 and AtKC1. Taken together, these findings suggest an essential role of AtKC1-like subunits for root K(+) uptake and K(+) homeostasis when plants experience conditions of K(+) limitation.

Indexed as

Gene Expression Regulation, PlantArabidopsisArabidopsis ProteinsBiophysicsElectrophysiologyHomeostasisModels, BiologicalMutationPlant Physiological PhenomenaPlant RootsPotassiumPotassium ChannelsProtein SubunitsTwo-Hybrid System TechniquesAKT1 protein, ArabidopsisArabidopsis ProteinsPotassiumPotassium ChannelsProtein Subunits

Identifiers

PMID19509299
PMCPMC2755853
OpenAlexW1506282373

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.