Evidence map›Paper›PMID 36971909›Full record

ArticleMolecular biology reports2023

Proteomics analysis of a tobacco variety resistant to brown spot disease and functional characterization of NbMLP423 in Nicotiana benthamiana.

Yu Zhang, Jie Wang, Yong Xiao, Caihong Jiang, Lirui Cheng, Shiping Guo, Chenggang Luo, Yuanying Wang, Haijiang Jia

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Comprehensive analysis of theForestry research · 2026
    Article
  3. 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

9 authors at 4 institutions in 1 country.

Yu ZhangTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, 266101, People's Republic of China.
Jie WangTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, 266101, People's Republic of China.
Yong XiaoSichuan Tobacco Company, Chengdu, 610000, People's Republic of China.
Caihong JiangTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, 266101, People's Republic of China.
Lirui ChengTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, 266101, People's Republic of China.
Shiping GuoSichuan Tobacco Company, Chengdu, 610000, People's Republic of China.
Chenggang LuoTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, 266101, People's Republic of China. wangjetby@163.com.
Yuanying WangTobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, 266101, People's Republic of China. wangyuanying@caas.cn.
Haijiang JiaRaw Material Technology Center of Guangxi Tobacco, Nanning, 530000, China. jia053@163.com.
Chinese Academy of Agricultural Sciences · CNChina Tobacco · CNTobacco Research Institute · CNChina Tobacco Guangxi Industrial (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTobacco brown spot disease is an important disease caused by Alternaria alternata that affects tobacco production and quality worldwide. Planting resistant varieties is the most economical and effective way to control this disease. However, the lack of understanding of the mechanism of tobacco resistance to tobacco brown spot has hindered progress in the breeding of resistant varieties. METHODS AND

resultsIn this study, differentially expressed proteins (DEPs), including 12 up-regulated and 11 down-regulated proteins, were screened using isobaric tags for relative and absolute quantification (iTRAQ) by comparing resistant and susceptible pools and analyzing the associated functions and metabolic pathways. Significantly up-regulated expression of the major latex-like protein gene 423 (MLP 423) was detected in both the resistant parent and the population pool. Bioinformatics analysis showed that the NbMLP423 cloned in Nicotiana benthamiana had a similar structure to the NtMLP423 in Nicotiana tabacum, and that expression of both genes respond rapidly to Alternaria alternata infection. NbMLP423 was then used to study the subcellular localization and expression in different tissues, followed by both silencing and the construction of an overexpression system for NbMLP423. The silenced plants demonstrated inhibited TBS resistance, while the overexpressed plants exhibited significantly enhanced resistance. Exogenous applications of plant hormones, such as salicylic acid, had a significant inducing effect on NbMLP423 expression.

conclusionsTaken together, our results provide insights into the role of NbMLP423 in plants against tobacco brown spot infection and provide a foundation for obtaining resistant tobacco varieties through the construction of new candidate genes of the MLP subfamily.

Indexed as

NicotianaPlant ProteinsAlternariaPlant BreedingPlant DiseasesProteomicsPlant ProteinsAlternaria alternateDEPsiTRAQMLP423Tobacco brown spot

Identifiers

PMID36971909
OpenAlexW4361011202

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.