Evidence map›Paper›PMID 42316005›Full record

ArticleBMC plant biology2026

Distinct Mg²⁺ responses and species-specific transcriptional regulation of the magnesium transporter MGR2 in Saccharum officinarum and Saccharum spontaneum.

Huihong Shi, Dadong Lin, Xiuting Hua, Zhongmou Yu, Zhen Li, Cheng He, Yuhong Lan, Hongyan Ding, Wei Gu, Hai Zhang and 2 more

Abstract read
In one paragraph

Article in BMC plant biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Huihong Shi *Guangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Dadong Lin *Center for Genomics and Biotechnology, National Sugarcane Engineering Technology Research Center, Fujian Provincial Key Laboratory of Haixia Applied Plant Systems Biology, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Xiuting Hua *Guangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Zhongmou YuGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Zhen LiGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Cheng HeGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Yuhong LanGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Hongyan DingGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Wei GuGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Hai ZhangGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China.
Qiutao XuGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China. qiutaoxu@gxu.edu.cn.
Jisen ZhangGuangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, Nanning, Guangxi, 530004, China. zjisen@126.com.

Funding

Guangxi Science and Technology Major Program AD25069107, AB24153006, and AA24206023, 2025FNFN99006 and AA24206006National Key Research and Development Program of China 2024YFF1000800National Natural Science Foundation of China 32272196 and U24A20387
6 · The paper itself

Abstract

backgroundMagnesium (Mg²⁺) is essential for chlorophyll synthesis, enzyme activation, and photosynthesis, but the differential regulation of Mg²⁺ homeostasis between the two founding Saccharum species (Saccharum officinarum and Saccharum spontaneum) remains unknown.

resultsWe systematically characterized the MGR gene family in S. spontaneum and S. officinarum and uncovered distinct physiological responses to Mg²⁺ availability between the two species. Comparative expression analysis across the leaf developmental gradient and diurnal cycles revealed species-specific transcriptional dynamics of MGR2, suggesting divergent regulatory mechanisms underlying Mg²⁺ management. Functional complementation in the Mg²⁺-deficient Salmonella typhimurium MM281 mutant demonstrated that both SsMGR2 and SoMGR2 restore Mg²⁺ uptake, confirming their conserved transport capability. Overexpression of SsMGR2 in rice conferred increased biomass under Mg²⁺ deficiency and enhanced tolerance to Mg²⁺ excess, indicating a broad role for this gene in Mg²⁺ homeostasis. Promoter architecture and transcription factor prediction further revealed interspecific divergence, with BBX25, COL5, and WRKY19-2 exhibiting species-dependent regulatory interactions that potentially explain the observed differences in MGR2 expression.

conclusionOverall, the research results indicate that S. spontaneum and S. officinarum exhibit different Mg²⁺ responses and MGR2 regulatory patterns, highlighting the distinct strategies for Mg²⁺ homeostasis in these two founding species. This work provides new insights into the transport mechanism of Mg²⁺ in sugarcane and preliminarily identifies candidate genes and regulatory factors for improving nutrient efficiency and stress recovery ability.

Indexed as

Cation Transport ProteinsGene Expression Regulation, PlantMagnesiumPlant ProteinsSaccharumHomeostasisOryzaPhylogenyPromoter Regions, GeneticSpecies SpecificityTranscription FactorsCation Transport ProteinsMagnesiumPlant ProteinsTranscription FactorsGene expressionGene regulationMg²⁺ release transportersSaccharum

Identifiers

PMID42316005
PMCPMC13523378

What Socratic 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 Socratic graph.