Evidence map›Paper›PMID 19050080›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

A PIIB-type Ca2+-ATPase is essential for stress adaptation in Physcomitrella patens.

Enas Qudeimat, Alexander M C Faltusz, Glen Wheeler, Daniel Lang, Hauke Holtorf, Colin Brownlee, Ralf Reski, Wolfgang Frank

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
  2. Review
  3. OsACA9, an Autoinhibited CaInternational journal of molecular sciences · 2024
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  14. Tonoplast-localized CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. ABA-Induced Vegetative Diaspore Formation inFrontiers in plant science · 2019
    Article
  16. Simultaneous imaging and functional studies reveal a tight correlation between calcium and actin networks.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 5 countries.

Enas QudeimatPlant Biotechnology, Institute of Biology II, Faculty of Biology, University of Freiburg, Schänzlestrasse 1, 79104 Freiburg, Germany.
Alexander M C Faltusz
Glen Wheeler
Daniel Lang
Hauke Holtorf
Colin Brownlee
Ralf Reski
Wolfgang Frank
Biotechnology Institute · USMarine Biological Association of the United Kingdom · GBPlant Biotechnology Institute · CAUniversity of Freiburg · DE

Funding

Biotechnology and Biological Sciences Research Council REI20579
6 · The paper itself

Abstract

Transient cytosolic Ca(2+) ([Ca(2+)](cyt)) elevations are early events in plant signaling pathways including those related to abiotic stress. The restoration of [Ca(2+)](cyt) to prestimulus levels involves ATP-driven Ca(2+) pumps, but direct evidence for an essential role of a plant Ca(2+)-ATPase in abiotic stress adaptation is missing. Here, we report on a stress-responsive Ca(2+)-ATPase gene (PCA1) from the moss Physcomitrella patens. Functional analysis of PCA1 in a Ca(2+) transport-deficient yeast mutant suggests that PCA1 encodes a P(IIB)-type Ca(2+)-ATPase harboring an N-terminal autoinhibitory domain. In vivo localizations identified membranes of small vacuoles as the integration site for a PCA1:GFP fusion protein. PCA1 mRNA levels are up-regulated by dehydration, NaCl, and abscisic acid, and PCA1 loss-of-function mutants (DeltaPCA1) exhibit an enhanced susceptibility to salt stress. The DeltaPCA1 lines show sustained elevated [Ca(2+)](cyt) in response to salt treatment in contrast to WT that shows transient Ca(2+) elevations, indicating a direct role for PCA1 in the restoration of prestimulus [Ca(2+)](cyt). The altered Ca(2+) response of the DeltaPCA1 mutant lines correlates with altered expression levels of stress-induced genes, suggesting disturbance of a stress-associated signaling pathway. We propose that PCA1 is an essential component for abiotic stress adaptation in Physcomitrella involved in the generation of a specific salt-induced Ca(2+) signature.

Indexed as

Abscisic AcidBryopsidaCalciumCalcium SignalingCalcium-Transporting ATPasesDesiccationGene Expression Regulation, EnzymologicGene Expression Regulation, PlantMolecular Sequence DataMutagenesisOsmotic PressurePlants, Genetically ModifiedSaccharomyces cerevisiaeSaltsSalt ToleranceStress, PhysiologicalAbscisic AcidCalciumCalcium-Transporting ATPasesSalts

Identifiers

PMID19050080
PMCPMC2614799
OpenAlexW2109297550

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.