Evidence map›Paper›PMID 25862728›Full record

ArticleMolecular & cellular proteomics : MCP2015

A Novel Function for Arabidopsis CYCLASE1 in Programmed Cell Death Revealed by Isobaric Tags for Relative and Absolute Quantitation (iTRAQ) Analysis of Extracellular Matrix Proteins.

Sarah J Smith, Johan T M Kroon, William J Simon, Antoni R Slabas, Stephen Chivasa

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.2field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  7. In vitro selection of blackberry (Plant biotechnology (Tokyo, Japan) · 2022
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  8. EspF of EnterohemorrhagicFrontiers in microbiology · 2022
    Article
  9. Article
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  11. Review
  12. Glycosylphosphatidylinositol-Anchored Proteins inFrontiers in plant science · 2019
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Regulatory Proteolysis in Arabidopsis-Pathogen Interactions.International journal of molecular sciences · 2015
    Review
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

5 authors at 1 institution in 1 country.

Sarah J SmithFrom the ‡School of Biological and Biomedical Sciences, Durham University, Durham DH1 3LE, United Kingdom.
Johan T M KroonFrom the ‡School of Biological and Biomedical Sciences, Durham University, Durham DH1 3LE, United Kingdom.
William J SimonFrom the ‡School of Biological and Biomedical Sciences, Durham University, Durham DH1 3LE, United Kingdom.
Antoni R SlabasFrom the ‡School of Biological and Biomedical Sciences, Durham University, Durham DH1 3LE, United Kingdom.
Stephen ChivasaFrom the ‡School of Biological and Biomedical Sciences, Durham University, Durham DH1 3LE, United Kingdom stephen.chivasa@durham.ac.uk.
Durham University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H000283/1
6 · The paper itself

Abstract

Programmed cell death is essential for plant development and stress adaptation. A detailed understanding of the signal transduction pathways that regulate plant programmed cell death requires identification of the underpinning protein networks. Here, we have used a protagonist and antagonist of programmed cell death triggered by fumonisin B1 as probes to identify key cell death regulatory proteins in Arabidopsis. Our hypothesis was that changes in the abundance of cell death-regulatory proteins induced by the protagonist should be blocked or attenuated by concurrent treatment with the antagonist. We focused on proteins present in the mobile phase of the extracellular matrix on the basis that they are important for cell-cell communications during growth and stress-adaptive responses. Salicylic acid, a plant hormone that promotes programmed cell death, and exogenous ATP, which can block fumonisin B1-induced cell death, were used to treat Arabidopsis cell suspension cultures prior to isobaric-tagged relative and absolute quantitation analysis of secreted proteins. A total of 33 proteins, whose response to salicylic acid was suppressed by ATP, were identified as putative cell death-regulatory proteins. Among these was CYCLASE1, which was selected for further analysis using reverse genetics. Plants in which CYCLASE1 gene expression was knocked out by insertion of a transfer-DNA sequence manifested dramatically increased cell death when exposed to fumonisin B1 or a bacterial pathogen that triggers the defensive hypersensitive cell death. Although pathogen inoculation altered CYCLASE1 gene expression, multiplication of bacterial pathogens was indistinguishable between wild type and CYCLASE1 knockout plants. However, remarkably severe chlorosis symptoms developed on gene knockout plants in response to inoculation with either a virulent bacterial pathogen or a disabled mutant that is incapable of causing disease in wild type plants. These results show that CYCLASE1, which had no known function hitherto, is a negative regulator of cell death and regulates pathogen-induced symptom development in Arabidopsis.

Indexed as

Adenosine TriphosphateArabidopsisArabidopsis ProteinsCell DeathExtracellular Matrix ProteinsFumonisinsProteomicsPseudomonas syringaeSalicylic AcidAdenosine TriphosphateArabidopsis ProteinsExtracellular Matrix Proteinsfumonisin B1FumonisinsSalicylic Acid

Identifiers

PMID25862728
PMCPMC4458720
OpenAlexW2255979074

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.