Evidence map›Paper›PMID 35039546›Full record

ArticleScientific reports2022

Analysis of NIA and GSNOR family genes and nitric oxide homeostasis in response to wheat-leaf rust interaction.

Deepak T Hurali, Ramesh Bhurta, Sandhya Tyagi, Lekshmy Sathee, Adavi B Sandeep, Dalveer Singh, Niharika Mallick, Vinod, Shailendra K Jha

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Effect ofInternational journal of molecular sciences · 2022
    Article
  5. 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

9 authors at 1 institution in 1 country.

Deepak T Hurali *Division of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
Ramesh Bhurta *Division of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
Sandhya TyagiDivision of Plant Physiology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
Lekshmy SatheeDivision of Plant Physiology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India. lekshmyrnair@gmail.com.
Adavi B SandeepDivision of Plant Physiology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
Dalveer SinghDivision of Plant Physiology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
Niharika MallickDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
VinodDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
Shailendra K JhaDivision of Genetics, ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India. jhashail78@gmail.com.
Indian Agricultural Research Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nitric oxide (NO) modulates plant response to biotic and abiotic stresses by S-nitrosylation-mediated protein post-translational modification. Nitrate reductase (NR) and S-nitrosoglutathione reductase (GSNOR) enzymes are essential for NO synthesis and the maintenance of Nitric oxide/S-nitroso glutathione (NO/GSNO) homeostasis, respectively. S-nitrosoglutathione, formed by the S-nitrosylation reaction of NO with glutathione, plays a significant physiological role as the mobile reservoir of NO. The genome-wide analysis identified nine NR (NIA) and three GSNOR genes in the wheat genome. Phylogenic analysis revealed that the nine NIA genes +were clustered into four groups and the 3 GSNORs into two groups. qRT-PCR expression profiling of NIAs and GSNORs was done in Chinese spring (CS), a leaf rust susceptible wheat line showing compatible interaction, and Transfer (TR), leaf rust-resistant wheat line showing incompatible interaction, post-inoculation with leaf rust pathotype 77-5 (121-R-63). All the NIA genes showed upregulation during incompatible interaction in comparison with the compatible reaction. The GSNOR genes showed a variable pattern of expression: the TaGSNOR1 showed little change, whereas TaGSNOR2 showed higher expression during the incompatible response. TaGSNOR3 showed a rise of expression both in compatible and incompatible reactions. Before inoculation and after 72 h of pathogen inoculation, NO localization was studied in both compatible and incompatible reactions. The S-nitrosothiol accumulation, NR, and glutathione reductase activity showed a consistent increase in the incompatible interactions. The results demonstrate that both NR and GSNOR plays significant role in defence against the leaf rust pathogen in wheat by modulating NO homeostasis or signalling.

Indexed as

Aldehyde OxidoreductasesGene Expression Regulation, PlantGenome, PlantHomeostasisNitrate ReductaseNitric OxidePlant DiseasesProtein Processing, Post-TranslationalSignal TransductionStress, PhysiologicalTriticumAldehyde Oxidoreductasesformaldehyde dehydrogenase, glutathione-independentNitrate ReductaseNitric Oxide

Identifiers

PMID35039546
PMCPMC8764060
OpenAlexW4205149735

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.