Evidence map›Paper›PMID 40405085›Full record

ArticleBMC plant biology2025

Genome-wide identification, molecular docking and expression analysis of enzymes involved in the primary and secondary metabolic branching points of the selenium metabolic pathway in Cardamine hupingshanensis.

Yue Xu, Lilong Gao, Jingyi Liu, Wenwu Guan, Jingyu Xie, Xixi Zeng, Yushan Chen, Yanke Lu, Zhi Hou, Zhixin Xiang and 2 more

Abstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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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.

Yue Xu *Hubei Key Laboratory of Biological Resources Protection and Utilization, Hubei Minzu University, Enshi, 44500, China.
Lilong Gao *Hubei Key Laboratory of Biological Resources Protection and Utilization, Hubei Minzu University, Enshi, 44500, China.
Jingyi LiuCollage of Biological and Food Engineering, Hubei Minzu University, Enshi, 44500, China.
Wenwu GuanCollage of Biological and Food Engineering, Hubei Minzu University, Enshi, 44500, China.
Jingyu XieHubei Key Laboratory of Biological Resources Protection and Utilization, Hubei Minzu University, Enshi, 44500, China.
Xixi ZengCollage of Forestry and Horticulture, Hubei Minzu University, Enshi, 44500, China.
Yushan ChenHubei Key Laboratory of Biological Resources Protection and Utilization, Hubei Minzu University, Enshi, 44500, China.
Yanke LuCollage of Biological and Food Engineering, Hubei Minzu University, Enshi, 44500, China.
Zhi HouCollage of Biological and Food Engineering, Hubei Minzu University, Enshi, 44500, China.
Zhixin XiangCollage of Biological and Food Engineering, Hubei Minzu University, Enshi, 44500, China.
Yifeng ZhouHubei Key Laboratory of Biological Resources Protection and Utilization, Hubei Minzu University, Enshi, 44500, China. 77416757@qq.com.
Qiaoyu TangHubei Key Laboratory of Biological Resources Protection and Utilization, Hubei Minzu University, Enshi, 44500, China. 330375856@qq.com.

Funding

he Open Fund of Hubei Key Laboratory of Biological Resources Protection and Utilization KYPT012301National Natural Science Foundation of China 32260070the Excellent Young and Middle-aged Scientific and Technological Innovation Team Projects of Colleges and Universities in Hubei Province T2020020
6 · The paper itself

Abstract

backgroundCardamine hupingshanensis is a plant known for its unique selenium tolerance, making it a key model for selenium metabolism research. Adenosine phosphosulfate kinase (APK) and adenosine phosphosulfate reductase (APR) are widely distributed in plants and play a crucial role in selenium metabolism. While genome-wide analyses of the APK and APR families have been conducted across various plant species, a systematic identification and analysis of these gene families in Cardamine hupingshanensis is still lacking.

resultsThere are 7 ChAPK and 5 ChAPR genes identified from the genome of C. hupingshanensis, which can be classified into 4 subfamilies for ChAPK and 3 subfamilies for ChAPR, respectively. All these members share similar conserved motifs and gene structures. Phylogenetic and promoter analyses suggest they are involved in environmental responses, phytohormone regulation, and light signalling. Molecular docking analysis indicated that ChAPK enzymes have a higher affinity for adenosine phosphoselenate (APSe) compared to ChAPR. In 3D interaction force analysis, residues such as His

conclusionsAll members of ChAPK and ChAPR families have a strong affinity for APSe and are regulated by the redox state. However, only three members of ChAPK (ChAPK1-1, ChAPK1-2, and ChAPK4-2) are regulated by the redox state, and these are located in the chloroplast. Furthermore, low concentrations of selenium in the nutrient solution can promote antioxidant activity in the leaves of C. hupingshanensis seedlings, whereas high concentrations of selenium exhibit the opposite effect, as confirmed by the results of oxidative metabolite and antioxidant enzyme assays.

Indexed as

CardaminePlant ProteinsSeleniumGene Expression Regulation, PlantGenome, PlantGenome-Wide Association StudyMetabolic Networks and PathwaysMolecular Docking SimulationOxidoreductases Acting on Sulfur Group DonorsPhylogenyadenylylsulfate reductaseOxidoreductases Acting on Sulfur Group DonorsPlant ProteinsSeleniumAdenosine phosphosulfate kinaseAdenosine phosphosulfate reductaseCardamine hupingshanensisGene expressionMolecular docking

Identifiers

PMID40405085
PMCPMC12096557

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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.