Evidence map›Paper›PMID 39264953›Full record

ArticlePLoS genetics2024

Subfunctionalization of NRC3 altered the genetic structure of the Nicotiana NRC network.

Ching-Yi Huang, Yu-Seng Huang, Yu Sugihara, Hung-Yu Wang, Lo-Ting Huang, Juan Carlos Lopez-Agudelo, Yi-Feng Chen, Kuan-Yu Lin, Bing-Jen Chiang, AmirAli Toghani and 4 more

Abstract read
In one paragraph

Article in PLoS genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

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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

4 citing papers in PubMed.

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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

14 authors.

Ching-Yi HuangInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.ORCID https://orcid.org/0009-0000-0002-5716
Yu-Seng HuangInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.ORCID https://orcid.org/0009-0005-2578-4299
Yu SugiharaThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich, United Kingdom.ORCID https://orcid.org/0000-0001-6042-1091
Hung-Yu WangInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
Lo-Ting HuangInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.ORCID https://orcid.org/0009-0001-8280-893X
Juan Carlos Lopez-AgudeloInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.ORCID https://orcid.org/0009-0000-2152-3853
Yi-Feng ChenInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
Kuan-Yu LinInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
Bing-Jen ChiangInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
AmirAli ToghaniThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich, United Kingdom.
Jiorgos KourelisThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich, United Kingdom.ORCID https://orcid.org/0000-0002-9007-1333
Chun-Hsiung WangInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.ORCID https://orcid.org/0000-0003-2242-7200
Lida DerevninaCrop Science Center, Department of Plant Sciences, University of Cambridge, Cambridge, United Kingdom.
Chih-Hang WuInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.ORCID https://orcid.org/0000-0003-1616-1872

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleotide-binding domain and leucine-rich repeat (NLR) proteins play crucial roles in immunity against pathogens in both animals and plants. In solanaceous plants, activation of several sensor NLRs triggers their helper NLRs, known as NLR-required for cell death (NRC), to form resistosome complexes to initiate immune responses. While the sensor NLRs and downstream NRC helpers display diverse genetic compatibility, molecular evolutionary events leading to the complex network architecture remained elusive. Here, we showed that solanaceous NRC3 variants underwent subfunctionalization after the divergence of Solanum and Nicotiana, altering the genetic architecture of the NRC network in Nicotiana. Natural solanaceous NRC3 variants form three allelic groups displaying distinct compatibilities with the sensor NLR Rpi-blb2. Ancestral sequence reconstruction and analyses of natural and chimeric variants identified six key amino acids involved in sensor-helper compatibility. These residues are positioned on multiple surfaces of the resting NRC3 homodimer, collectively contributing to their compatibility with Rpi-blb2. Upon activation, Rpi-blb2-compatible NRC3 variants form membrane-associated punctate and high molecular weight complexes, and confer resistance to the late blight pathogen Phytophthora infestans. Our findings revealed how mutations in NRC alleles lead to subfunctionalization, altering sensor-helper compatibility and contributing to the increased complexity of the NRC network.

Indexed as

NicotianaNLR ProteinsPlant ProteinsAllelesDisease ResistanceEvolution, MolecularPhytophthora infestansPlant DiseasesPlant ImmunitySolanumNLR ProteinsPlant Proteins

Identifiers

PMID39264953
PMCPMC11421798

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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.