Evidence map›Paper›PMID 26232921›Full record

ArticlePlanta2015

Quantitative proteomics analysis reveals that S-nitrosoglutathione reductase (GSNOR) and nitric oxide signaling enhance poplar defense against chilling stress.

Tielong Cheng, Jinhui Chen, Abd Allah Ef, Pengkai Wang, Guangping Wang, Xiangyang Hu, Jisen Shi

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Planta, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
16.0field-weighted citation impact, top 1% 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

26 citing papers in PubMed, 69 citations in OpenAlex.

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  10. Hydrogen Sulfide Signaling ProtectsFrontiers in plant science · 2020
    Article
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  13. Review
  14. Elevated COProtoplasma · 2019
    Article
  15. Article
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  17. Review
  18. Overexpression of E3 Ubiquitin Ligase GeneFrontiers in plant science · 2017
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Tielong ChengKey Laboratory of Forest Genetics & Biogeography, Ministry of Education, Nanjing Forest University, Nanjing, 210037, China.
Jinhui ChenKey Laboratory of Forest Genetics & Biogeography, Ministry of Education, Nanjing Forest University, Nanjing, 210037, China.
Abd Allah EfDepartment of Plant Production, Faculty of Food & Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Pengkai WangKey Laboratory of Forest Genetics & Biogeography, Ministry of Education, Nanjing Forest University, Nanjing, 210037, China.
Guangping WangKey Laboratory of Forest Genetics & Biogeography, Ministry of Education, Nanjing Forest University, Nanjing, 210037, China.
Xiangyang HuKey Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming, 650201, China. huxiangyang@mail.kib.ac.cn.
Jisen ShiKey Laboratory of Forest Genetics & Biogeography, Ministry of Education, Nanjing Forest University, Nanjing, 210037, China. jshi@njfu.edu.cn.
Nanjing Forestry University · CNAcademia Sinica · TWKing Saud University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MAIN

conclusionNO acts as the essential signal to enhance poplar tolerance to chilling stress via antioxidant enzyme activities and protein S -nitrosylation modification, NO signal is also strictly controlled by S -nitrosoglutathione reductase and nitrate reductase to avoid the over-accumulation of reactive nitrogen species. Poplar (Populus trichocarpa) are fast growing woody plants with both ecological and economic value; however, the mechanisms by which poplar adapts to environmental stress are poorly understood. In this study, we used isobaric tags for relative and absolute quantification proteomic approach to characterize the response of poplar exposed to cold stress. We identified 114 proteins that were differentially expressed in plants exposed to cold stress. In particular, some of the proteins are involved in reactive oxygen species (ROS) and reactive nitrogen species (RNS) metabolism. Further physiological analysis showed that nitric oxide (NO) signaling activated a series of downstream defense responses. We further demonstrated that NO activated antioxidant enzyme activities and S-nitrosoglutathione reductase (GSNOR) activities, which would reduce ROS and RNS toxicity and thereby enhance poplar tolerance to cold stress. Suppressing NO accumulation or GSNOR activity aggravated cold damage to poplar leaves. Moreover, our results showed that RNS can suppress the activities of GSNOR and NO nitrate reductase (NR) by S-nitrosylation to fine-tune the NO signal and modulate ROS levels by modulating the S-nitrosylation of ascorbate peroxidase protein. Hence, our data demonstrate that NO signaling activates multiple pathways that enhance poplar tolerances to cold stress, and that NO signaling is strictly controlled through protein post-translational modification by S-nitrosylation.

Indexed as

Cold TemperatureProteomicsAldehyde OxidoreductasesNitric OxidePopulusReactive Nitrogen SpeciesSignal TransductionStress, PhysiologicalAldehyde Oxidoreductasesformaldehyde dehydrogenase, glutathione-independentNitric OxideReactive Nitrogen SpeciesCold stressNitric oxidePoplarProteomeS-Nitrosoglutathione reductase

Identifiers

PMID26232921
OpenAlexW1037789279

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.