Evidence map›Paper›PMID 32286394›Full record

ArticleScientific reports2020

OsNPR3.3-dependent salicylic acid signaling is involved in recessive gene xa5-mediated immunity to rice bacterial blight.

Guanghuai Jiang, Dedong Yin, Yue Shi, Zhuangzhi Zhou, Chunrong Li, Pengcheng Liu, Yanfeng Jia, Yanyan Wang, Zhenzhen Liu, Minxiang Yu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
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

13 authors at 3 institutions in 1 country.

Guanghuai Jiang *Center for Molecular Agrobiology,Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Dedong Yin *State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Yue ShiCenter for Molecular Agrobiology,Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Zhuangzhi ZhouState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Chunrong LiCenter for Molecular Agrobiology,Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Pengcheng LiuCenter for Molecular Agrobiology,Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Yanfeng JiaCenter for Molecular Agrobiology,Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Yanyan WangCenter for Molecular Agrobiology,Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Zhenzhen LiuCenter for Molecular Agrobiology,Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Minxiang YuState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Xianghong WuState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Wenxue ZhaiCenter for Molecular Agrobiology,Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China. wxzhai@genetics.ac.cn.
Lihuang ZhuState Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China. lhzhu@genetics.ac.cn.
Chinese Academy of Sciences · CNInstitute of Genetics and Developmental Biology · CNState Key Laboratory of Plant Genomics · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Salicylic acid (SA) is a key natural component that mediates local and systemic resistance to pathogens in many dicotyledonous species. However, its function is controversial in disease resistance in rice plants. Here, we show that the SA signaling is involved in both pathogen-associated-molecular-patterns triggered immunity (PTI) and effector triggered immunity (ETI) to Xanthomonas oryzae pv. Oryzae (Xoo) mediated by the recessive gene xa5, in which OsNPR3.3 plays an important role through interacting with TGAL11. Rice plants containing homozygous xa5 gene respond positively to exogenous SA, and their endogenous SA levels are also especially induced upon infection by the Xoo strain, PXO86. Depletion of endogenous SA can significantly attenuate plant resistance to PXO86, even to 86∆HrpXG (mutant PXO86 with a damaged type III secretion system). These results indicated that SA plays an important role in disease resistance in rice plants, which can be clouded by high levels of endogenous SA and the use of particular rice varieties.

Indexed as

Bacterial ProteinsDisease ResistanceGene Expression Regulation, PlantGenes, PlantGenes, RecessiveHost-Pathogen InteractionsMutationOryzaPlant DiseasesPlant ProteinsProtein IsoformsSalicylic AcidSeedlingsSignal TransductionTranscription FactorsXanthomonasBacterial ProteinsHrpX protein, BacteriaPlant ProteinsProtein IsoformsSalicylic AcidTranscription Factors

Identifiers

PMID32286394
PMCPMC7156675
OpenAlexW3015474085

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.