Evidence map›Paper›PMID 26601946›Full record

ArticleThe Journal of biological chemistry2016

The Tomato Nucleotide-binding Leucine-rich Repeat Immune Receptor I-2 Couples DNA-binding to Nucleotide-binding Domain Nucleotide Exchange.

Stepan Fenyk, Christopher H Dixon, William H Gittens, Philip D Townsend, Gary J Sharples, Lars-Olof Pålsson, Frank L W Takken, Martin J Cann

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
6.7field-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

8 citing papers in PubMed, 23 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

8 authors at 2 institutions in 2 countries.

Stepan FenykFrom the School of Biological and Biomedical Sciences, the Biophysical Sciences Institute, and.
Christopher H DixonFrom the School of Biological and Biomedical Sciences, the Biophysical Sciences Institute, and.
William H GittensFrom the School of Biological and Biomedical Sciences, the Biophysical Sciences Institute, and.
Philip D TownsendFrom the School of Biological and Biomedical Sciences, the Biophysical Sciences Institute, and.
Gary J SharplesFrom the School of Biological and Biomedical Sciences, the Biophysical Sciences Institute, and.
Lars-Olof Pålssonthe Department of Chemistry, Durham University, South Road, Durham DH1 3LE, United Kingdom and.
Frank L W Takkenthe Molecular Plant Pathology, Swammerdam Institute for Life Sciences, University of Amsterdam, 1098 XH, Amsterdam, The Netherlands.
Martin J CannFrom the School of Biological and Biomedical Sciences, the Biophysical Sciences Institute, and m.j.cann@durham.ac.uk.
Durham University · GBUniversity of Amsterdam · NL

Funding

Biotechnology and Biological Sciences Research Council BB/M007405/1
6 · The paper itself

Abstract

Plant nucleotide-binding leucine-rich repeat (NLR) proteins enable plants to recognize and respond to pathogen attack. Previously, we demonstrated that the Rx1 NLR of potato is able to bind and bend DNA in vitro. DNA binding in situ requires its genuine activation following pathogen perception. However, it is unknown whether other NLR proteins are also able to bind DNA. Nor is it known how DNA binding relates to the ATPase activity intrinsic to NLR switch function required to immune activation. Here we investigate these issues using a recombinant protein corresponding to the N-terminal coiled-coil and nucleotide-binding domain regions of the I-2 NLR of tomato. Wild type I-2 protein bound nucleic acids with a preference of ssDNA ≈ dsDNA > ssRNA, which is distinct from Rx1. I-2 induced bending and melting of DNA. Notably, ATP enhanced DNA binding relative to ADP in the wild type protein, the null P-loop mutant K207R, and the autoactive mutant S233F. DNA binding was found to activate the intrinsic ATPase activity of I-2. Because DNA binding by I-2 was decreased in the presence of ADP when compared with ATP, a cyclic mechanism emerges; activated ATP-associated I-2 binds to DNA, which enhances ATP hydrolysis, releasing ADP-bound I-2 from the DNA. Thus DNA binding is a general property of at least a subset of NLR proteins, and NLR activation is directly linked to its activity at DNA.

Indexed as

Models, MolecularAdenosine DiphosphateAdenosine TriphosphatasesAdenosine TriphosphateAmino Acid SubstitutionBinding SitesDNA-Binding ProteinsDNA, Single-StrandedElectrophoretic Mobility Shift AssayHydrolysisLeucine-Rich Repeat ProteinsMutationNucleotide Transport ProteinsPeptide FragmentsPlant ImmunityPlant ProteinsAdenosine DiphosphateAdenosine TriphosphatasesAdenosine TriphosphateDNA-Binding ProteinsDNA, Single-StrandedLeucine-Rich Repeat ProteinsNucleotide Transport ProteinsPeptide FragmentsPlant ProteinsProteinsRecombinant ProteinsRNAATPases associated with diverse cellular activities (AAA)cellular immune responseDNA binding proteinNod-like receptor (NLR)nucleotideplant biochemistry

Identifiers

PMID26601946
PMCPMC4714197
OpenAlexW2239088618

What OpenQuestion holds

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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.