Evidence map›Paper›PMID 24914891›Full record

ArticlePloS one2014

The hnRNP-Q protein LIF2 participates in the plant immune response.

Clémentine Le Roux, Stefania Del Prete, Stéphanie Boutet-Mercey, François Perreau, Claudine Balagué, Dominique Roby, Mathilde Fagard, Valérie Gaudin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.1field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 68 citations in OpenAlex.

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  10. LeafamineInternational journal of molecular sciences · 2022
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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

8 authors at 2 institutions in 1 country.

Clémentine Le RouxINRA-AgroParisTech, UMR1318, Institut J.-P. Bourgin, Centre de Versailles-Grignon, Versailles, France.
Stefania Del PreteINRA-AgroParisTech, UMR1318, Institut J.-P. Bourgin, Centre de Versailles-Grignon, Versailles, France.
Stéphanie Boutet-MerceyINRA-AgroParisTech, UMR1318, Institut J.-P. Bourgin, Centre de Versailles-Grignon, Versailles, France.
François PerreauINRA-AgroParisTech, UMR1318, Institut J.-P. Bourgin, Centre de Versailles-Grignon, Versailles, France.
Claudine BalaguéINRA, Laboratoire des Interactions Plantes-Microorganismes (LIPM), UMR441, Castanet-Tolosan, France; CNRS, Laboratoire des Interactions Plantes-Microorganismes (LIPM), UMR2594, Castanet-Tolosan, France.
Dominique RobyINRA, Laboratoire des Interactions Plantes-Microorganismes (LIPM), UMR441, Castanet-Tolosan, France; CNRS, Laboratoire des Interactions Plantes-Microorganismes (LIPM), UMR2594, Castanet-Tolosan, France.
Mathilde FagardINRA-AgroParisTech, UMR1318, Institut J.-P. Bourgin, Centre de Versailles-Grignon, Versailles, France.
Valérie GaudinINRA-AgroParisTech, UMR1318, Institut J.-P. Bourgin, Centre de Versailles-Grignon, Versailles, France.
Institut Jean-Pierre Bourgin · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eukaryotes have evolved complex defense pathways to combat invading pathogens. Here, we investigated the role of the Arabidopsis thaliana heterogeneous nuclear ribonucleoprotein (hnRNP-Q) LIF2 in the plant innate immune response. We show that LIF2 loss-of-function in A. thaliana leads to changes in the basal expression of the salicylic acid (SA)- and jasmonic acid (JA)- dependent defense marker genes PR1 and PDF1.2, respectively. Whereas the expression of genes involved in SA and JA biosynthesis and signaling was also affected in the lif2-1 mutant, no change in SA and JA hormonal contents was detected. In addition, the composition of glucosinolates, a class of defense-related secondary metabolites, was altered in the lif2-1 mutant in the absence of pathogen challenge. The lif2-1 mutant exhibited reduced susceptibility to the hemi-biotrophic pathogen Pseudomonas syringae and the necrotrophic ascomycete Botrytis cinerea. Furthermore, the lif2-1 sid2-2 double mutant was less susceptible than the wild type to P. syringae infection, suggesting that the lif2 response to pathogens was independent of SA accumulation. Together, our data suggest that lif2-1 exhibits a basal primed defense state, resulting from complex deregulation of gene expression, which leads to increased resistance to pathogens with various infection strategies. Therefore, LIF2 may function as a suppressor of cell-autonomous immunity. Similar to its human homolog, NSAP1/SYNCRIP, a trans-acting factor involved in both cellular processes and the viral life cycle, LIF2 may regulate the conflicting aspects of development and defense programs, suggesting that a conserved evolutionary trade-off between growth and defense pathways exists in eukaryotes.

Indexed as

Plant ImmunityArabidopsisArabidopsis ProteinsBotrytisCyclopentanesGene Expression Regulation, PlantGene OntologyGlucosinolatesHeterogeneous-Nuclear RibonucleoproteinsModels, BiologicalMutationOxylipinsPlant DiseasesPseudomonas syringaeRNA-Binding ProteinsSalicylic AcidArabidopsis ProteinsCyclopentanesGlucosinolatesHeterogeneous-Nuclear Ribonucleoproteinsjasmonic acidLIF2 protein, ArabidopsisOxylipinsRNA-Binding ProteinsSalicylic Acid

Identifiers

PMID24914891
PMCPMC4051675
OpenAlexW1986985324

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.