Evidence map›Paper›PMID 25416475›Full record

ArticlePlant physiology2015

In planta processing and glycosylation of a nematode CLAVATA3/ENDOSPERM SURROUNDING REGION-like effector and its interaction with a host CLAVATA2-like receptor to promote parasitism.

Shiyan Chen, Ping Lang, Demosthenis Chronis, Sheng Zhang, Walter S De Jong, Melissa G Mitchum, Xiaohong Wang

Open access · greenAbstract read
In one paragraph

Article in Plant physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
10.3field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Article
  8. Plant immunity: Rice XA21-mediated resistance to bacterial infection.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
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  16. Article
  17. Signal Transduction in Plant⁻Nematode Interactions.International journal of molecular sciences · 2018
    Review
  18. Review
  19. Article
  20. Article
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

7 authors at 2 institutions in 2 countries.

Shiyan ChenDepartment of Plant Pathology and Plant-Microbe Biology (S.C., P.L., X.W.), Proteomics and Mass Spectrometry Facility, Institute of Biotechnology and Life Science Technologies (S.Z.), and Department of Plant Breeding and Genetics (W.S.D.J.), Cornell University, Ithaca, New York 14853;Robert W. Holley Center for Agriculture and Health, United States Department of Agriculture, Agricultural Research Service, Ithaca, New York 14853 (D.C., X.W.); andDivision of Plant Sciences and Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211 (M.G.M.).
Ping LangDepartment of Plant Pathology and Plant-Microbe Biology (S.C., P.L., X.W.), Proteomics and Mass Spectrometry Facility, Institute of Biotechnology and Life Science Technologies (S.Z.), and Department of Plant Breeding and Genetics (W.S.D.J.), Cornell University, Ithaca, New York 14853;Robert W. Holley Center for Agriculture and Health, United States Department of Agriculture, Agricultural Research Service, Ithaca, New York 14853 (D.C., X.W.); andDivision of Plant Sciences and Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211 (M.G.M.).
Demosthenis ChronisDepartment of Plant Pathology and Plant-Microbe Biology (S.C., P.L., X.W.), Proteomics and Mass Spectrometry Facility, Institute of Biotechnology and Life Science Technologies (S.Z.), and Department of Plant Breeding and Genetics (W.S.D.J.), Cornell University, Ithaca, New York 14853;Robert W. Holley Center for Agriculture and Health, United States Department of Agriculture, Agricultural Research Service, Ithaca, New York 14853 (D.C., X.W.); andDivision of Plant Sciences and Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211 (M.G.M.).
Sheng ZhangDepartment of Plant Pathology and Plant-Microbe Biology (S.C., P.L., X.W.), Proteomics and Mass Spectrometry Facility, Institute of Biotechnology and Life Science Technologies (S.Z.), and Department of Plant Breeding and Genetics (W.S.D.J.), Cornell University, Ithaca, New York 14853;Robert W. Holley Center for Agriculture and Health, United States Department of Agriculture, Agricultural Research Service, Ithaca, New York 14853 (D.C., X.W.); andDivision of Plant Sciences and Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211 (M.G.M.).
Walter S De JongDepartment of Plant Pathology and Plant-Microbe Biology (S.C., P.L., X.W.), Proteomics and Mass Spectrometry Facility, Institute of Biotechnology and Life Science Technologies (S.Z.), and Department of Plant Breeding and Genetics (W.S.D.J.), Cornell University, Ithaca, New York 14853;Robert W. Holley Center for Agriculture and Health, United States Department of Agriculture, Agricultural Research Service, Ithaca, New York 14853 (D.C., X.W.); andDivision of Plant Sciences and Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211 (M.G.M.).
Melissa G MitchumDepartment of Plant Pathology and Plant-Microbe Biology (S.C., P.L., X.W.), Proteomics and Mass Spectrometry Facility, Institute of Biotechnology and Life Science Technologies (S.Z.), and Department of Plant Breeding and Genetics (W.S.D.J.), Cornell University, Ithaca, New York 14853;Robert W. Holley Center for Agriculture and Health, United States Department of Agriculture, Agricultural Research Service, Ithaca, New York 14853 (D.C., X.W.); andDivision of Plant Sciences and Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211 (M.G.M.).
Xiaohong WangDepartment of Plant Pathology and Plant-Microbe Biology (S.C., P.L., X.W.), Proteomics and Mass Spectrometry Facility, Institute of Biotechnology and Life Science Technologies (S.Z.), and Department of Plant Breeding and Genetics (W.S.D.J.), Cornell University, Ithaca, New York 14853;Robert W. Holley Center for Agriculture and Health, United States Department of Agriculture, Agricultural Research Service, Ithaca, New York 14853 (D.C., X.W.); andDivision of Plant Sciences and Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211 (M.G.M.) xw57@cornell.edu.ORCID http://orcid.org/0000-0003-1790-4084
Cornell University · USUnited States Department of Agriculture · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Like other biotrophic plant pathogens, plant-parasitic nematodes secrete effector proteins into host cells to facilitate infection. Effector proteins that mimic plant CLAVATA3/ENDOSPERM SURROUNDING REGION-related (CLE) proteins have been identified in several cyst nematodes, including the potato cyst nematode (PCN); however, the mechanistic details of this cross-kingdom mimicry are poorly understood. Plant CLEs are posttranslationally modified and proteolytically processed to function as bioactive ligands critical to various aspects of plant development. Using ectopic expression coupled with nanoliquid chromatography-tandem mass spectrometry analysis, we show that the in planta mature form of proGrCLE1, a multidomain CLE effector secreted by PCN during infection, is a 12-amino acid arabinosylated glycopeptide (named GrCLE1-1Hyp4,7g) with striking structural similarity to mature plant CLE peptides. This glycopeptide is more resistant to hydrolytic degradation and binds with higher affinity to a CLAVATA2-like receptor (StCLV2) from potato (Solanum tuberosum) than its nonglycosylated forms. We further show that StCLV2 is highly up-regulated at nematode infection sites and that transgenic potatoes with reduced StCLV2 expression are less susceptible to PCN infection, indicating that interference of the CLV2-mediated signaling pathway confers nematode resistance in crop plants. These results strongly suggest that phytonematodes have evolved to utilize host cellular posttranslational modification and processing machinery for the activation of CLE effectors following secretion into plant cells and highlight the significance of arabinosylation in regulating nematode CLE effector activity. Our finding also provides evidence that multidomain CLEs are modified and processed similarly to single-domain CLEs, adding new insight into CLE maturation in plants.

Indexed as

AnimalsGlycopeptidesGlycosylationNematodaPlant DiseasesPlant ProteinsSignal TransductionSolanum tuberosumGlycopeptidesPlant Proteins

Identifiers

PMID25416475
PMCPMC4281011
OpenAlexW2000338836

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.