Evidence map›Paper›PMID 42152543›Full record

ArticlePlant, cell & environment2026

Enhanced Activity of Glutamine Synthetase by Manipulating a GWAS-Identified BnaA02.GLN1;2 Gene Augments Nitrate Uptake and Yield in Brassica napus.

Hao Zhang, Lulu Ren, Xuyou He, Haijiang Liu, Yidan Jing, Minhui Fan, Hongmei Cai, Sheliang Wang, Chuang Wang, Lei Shi and 3 more

Abstract read
In one paragraph

Article in Plant, cell & environment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Hao ZhangCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.
Lulu RenCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.
Xuyou HeCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.
Haijiang LiuCollege of Agronomy and Biotechnology, Southwest University, Chongqing, China.
Yidan JingCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.
Minhui FanCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.
Hongmei CaiCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.
Sheliang WangCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0002-9166-0578
Chuang WangCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0002-7663-7433
Lei ShiCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0002-5312-8521
Surya KantDepartment of Ecological, Plant and Animal Science, School of Agriculture, Biomedicine & Environment, La Trobe University, Bundoora, Victoria, Australia.
Fangsen XuCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0003-3564-1644
Guangda DingCollege of Resources and Environment/Microelement Research Center/Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0003-3702-5087

Funding

Biological Breeding-National Science and Technology Major Project 2023ZD04072
6 · The paper itself

Abstract

Exploiting natural variation to uncouple yield from nitrogen (N) input is essential for sustainable oilseed rape production. Here, we screened 505 accessions and discovered a 10-fold gradient in chlorate (ClO₃⁻) sensitivity that mirrors genotypic differences in nitrogen use efficiency (NUE). Chlorate-sensitive genotypes (CSG) exhibited 35% higher ¹⁵NO₃⁻ influx, 40%-62% greater root glutamine synthetase (GS) activity, and almost twice the seed yield of chlorate-insensitive genotypes (CIG) under high-N supply, whereas nitrate (NO₃⁻) reductase activity was unchanged. Chemical inhibition of GS using L-methionine-S-sulfoximine (MSX) resulted in the loss of ClO₃⁻ sensitivity, mechanistically linking assimilation flux to the observed phenotypic variation. Root proteomic analysis identified differentially abundant proteins between CSG and CIG and showed that BnaA02.GLN1;2 (a cytosolic GS1 homologue) was a hub protein with higher abundance in CSG. Overexpression of BnaA02.GLN1;2 enhanced rapeseed chlorate sensitivity under sufficient NO₃⁻ supply, promoted seedling growth, and enhanced both NO₃⁻ uptake and assimilation. Mature transgenic plants produced more pods and higher yields under normal N conditions while simultaneously reducing seed erucic acid and glucosinolate concentrations. Genome-wide association study mapped a major quantitative trait locus on chromosome A02, with BnaA02.GLN1;2 as the causal gene. Eleven single-nucleotide polymorphisms (SNPs) classified BnaA02.GLN1;2 into three haplotypes: BnaA02.GLN1;2

Indexed as

Brassica napusGenes, PlantGlutamate-Ammonia LigaseNitratesPlant ProteinsChloratesGene Expression Regulation, PlantGenome-Wide Association StudyGenotypeMethionine SulfoximineNitrogenPhenotypePlant RootsPlants, Genetically ModifiedQuantitative Trait LociSeedsChloratesGlutamate-Ammonia LigaseMethionine SulfoximineNitratesNitrogenPlant ProteinsBrassica napuschlorate sensitivitygenome‐wide association studyglutamine synthetasenitrate uptakenitrogen use efficiency

Identifiers

PMID42152543
PMCPMC13436454

What OpenQuestion holds

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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.