Evidence map›Paper›PMID 31729398›Full record

ArticleScientific reports2019

Deciphering signalling network in broad spectrum Near Isogenic Lines of rice resistant to Magnaporthe oryzae.

Priyanka Jain, Himanshu Dubey, Pankaj Kumar Singh, Amolkumar U Solanke, Ashok K Singh, T R Sharma

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Roles of maizeFrontiers in plant science · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Understanding the Dynamics of Blast Resistance in Rice-Journal of fungi (Basel, Switzerland) · 2022
    Review
  8. Article
  9. Recent Progress in Rice Broad-Spectrum Disease Resistance.International journal of molecular sciences · 2021
    Review
  10. Review
  11. Understanding Rice-Genes · 2021
    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

6 authors at 3 institutions in 1 country.

Priyanka JainICAR-National Institute for Plant Biotechnology, Pusa Campus, New Delhi, 110012, India.
Himanshu DubeyICAR-National Institute for Plant Biotechnology, Pusa Campus, New Delhi, 110012, India.
Pankaj Kumar SinghICAR-National Institute for Plant Biotechnology, Pusa Campus, New Delhi, 110012, India.
Amolkumar U SolankeICAR-National Institute for Plant Biotechnology, Pusa Campus, New Delhi, 110012, India.
Ashok K SinghICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
T R SharmaICAR-National Institute for Plant Biotechnology, Pusa Campus, New Delhi, 110012, India. trsharma@nabi.res.in.
National Research Centre on Plant Biotechnology · INIndian Agricultural Research Institute · INNational Agri-Food Biotechnology Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease resistance (R) genes like Pi9, Pita, Pi21, Pi54 are playing important role for broad spectrum blast resistance in rice. Development of near isogenic lines (NILs) using these type of broad spectrum genes and understanding their signalling networks is essential to cope up with highly evolving Magnaporthe oryzae strains for longer duration. Here, transcriptional-level changes were studied in three near-isogenic lines (PB1 + Pi1, PB1 + Pi9 and PB1 + Pi54) of rice resistant to blast infection, to find the loci that are unique to resistant lines developed in the background of Pusa Basmati 1 (PB1). The pathway analysis of loci, unique to resistant NILs compared to susceptible control revealed that plant secondary metabolite synthesis was the common mechanism among all NILs to counter against M. oryzae infection. Comparative transcriptome analysis helped to find out common clusters of co-expressed significant differentially expressed loci (SDEL) in both PB1 + Pi9 and PB1 + Pi54 NILs. SDELs from these clusters were involved in the synthesis and degradation of starch; synthesis and elongation of fatty acids; hydrolysis of phospholipids; synthesis of phenylpropanoid; and metabolism of ethylene and jasmonic acid. Through detailed analysis of loci specific to each resistant NIL, we identified a network of signalling pathways mediated by each blast resistance gene. The study also offers insights into transcriptomic dynamics, points to a set of important candidate genes that serve as module to regulate the changes in resistant NILs. We suggest that pyramiding of the blast resistance gene Pi9 with Pi54 will lead to maximum broad spectrum resistance to M. oryzae.

Indexed as

MagnaportheSignal TransductionComputational BiologyDisease ResistanceGene Expression Regulation, PlantGene OntologyGene Regulatory NetworksGenes, PlantHost-Pathogen InteractionsMolecular Sequence AnnotationOryzaPlant DiseasesPlants, Genetically Modified

Identifiers

PMID31729398
PMCPMC6858299
OpenAlexW2989134461

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Registered trials

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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.