Evidence map›Paper›PMID 28698366›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

NLR network mediates immunity to diverse plant pathogens.

Chih-Hang Wu, Ahmed Abd-El-Haliem, Tolga O Bozkurt, Khaoula Belhaj, Ryohei Terauchi, Jack H Vossen, Sophien Kamoun

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 195 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
195citing papers in PubMed, 1 pooled it
88.2field-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

195 citing papers in PubMed, 1 synthesis or guideline pooled it, 472 citations in OpenAlex.

  1. Pooled it
  2. Article
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Structure-informed engineering of plant-microbe interactions.The Plant journal : for cell and molecular biology · 2026
    Review
  9. Article
  10. Article
  11. Plant NLRs are getting into higher-order architectures.The Plant journal : for cell and molecular biology · 2026
    Review
  12. Review
  13. Subcellular calcium dynamics and organelle perturbations in resistosome-mediated cell death.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  14. Article
  15. Review
  16. Molecular mechanisms of plant NLR activation and signalling.The Plant journal : for cell and molecular biology · 2026
    Review
  17. Article
  18. Article
  19. Article
  20. Article

135 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Chih-Hang WuThe Sainsbury Laboratory, Norwich Research Park, Norwich NR4 7UH, United Kingdom.
Ahmed Abd-El-HaliemPlant Breeding, Wageningen University and Research, Wageningen 6708 PB, The Netherlands.
Tolga O BozkurtThe Sainsbury Laboratory, Norwich Research Park, Norwich NR4 7UH, United Kingdom.
Khaoula BelhajThe Sainsbury Laboratory, Norwich Research Park, Norwich NR4 7UH, United Kingdom.
Ryohei TerauchiDivision of Genomics and Breeding, Iwate Biotechnology Research Center, Iwate 024-0003, Japan.
Jack H VossenPlant Breeding, Wageningen University and Research, Wageningen 6708 PB, The Netherlands.
Sophien KamounThe Sainsbury Laboratory, Norwich Research Park, Norwich NR4 7UH, United Kingdom; sophien.kamoun@tsl.ac.uk.ORCID 0000-0002-0290-0315
Norwich Research Park · GBWageningen University & Research · NLKyoto University · JP

Funding

Biotechnology and Biological Sciences Research Council
6 · The paper itself

Abstract

Both plants and animals rely on nucleotide-binding domain and leucine-rich repeat-containing (NLR) proteins to respond to invading pathogens and activate immune responses. An emerging concept of NLR function is that "sensor" NLR proteins are paired with "helper" NLRs to mediate immune signaling. However, our fundamental knowledge of sensor/helper NLRs in plants remains limited. In this study, we discovered a complex NLR immune network in which helper NLRs in the NRC (NLR required for cell death) family are functionally redundant but display distinct specificities toward different sensor NLRs that confer immunity to oomycetes, bacteria, viruses, nematodes, and insects. The helper NLR NRC4 is required for the function of several sensor NLRs, including Rpi-blb2, Mi-1.2, and R1, whereas NRC2 and NRC3 are required for the function of the sensor NLR Prf. Interestingly, NRC2, NRC3, and NRC4 redundantly contribute to the immunity mediated by other sensor NLRs, including Rx, Bs2, R8, and Sw5. NRC family and NRC-dependent NLRs are phylogenetically related and cluster into a well-supported superclade. Using extensive phylogenetic analysis, we discovered that the NRC superclade probably emerged over 100 Mya from an NLR pair that diversified to constitute up to one-half of the NLRs of asterids. These findings reveal a complex genetic network of NLRs and point to a link between evolutionary history and the mechanism of immune signaling. We propose that this NLR network increases the robustness of immune signaling to counteract rapidly evolving plant pathogens.

Indexed as

Plant ImmunityEvolution, MolecularGene Regulatory NetworksNicotianaNLR ProteinsPlant DiseasesNLR Proteinsevolutionhost–microbe interactionsimmunity

Identifiers

PMID28698366
PMCPMC5544293
OpenAlexW2736049245

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.