Evidence map›Paper›PMID 41483159›Full record

ArticleProtoplasma2026

Elucidating brassinosteroid-mediated regulation of natural rubber biosynthesis in Taraxacum kok-saghyz through integrated transcriptomic and metabolomic analyses.

Hao Xie, Changping Zhang, Zihan Guo, Fengqi Luo, Yan Zhang, Jie Yan

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

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0citing papers in PubMed
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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hao XieCollege of life Sciences, Xinjiang Production and Construction Corps Key Laboratory of Oasis Town and Mountain-basin System Ecology, Key Laboratory of Xinjiang Phytomedicine Resource Utilization, Shihezi University, Ministry of Education, North 4th Road, Xinjiang, Shihezi, 832003, China.
Changping ZhangCollege of life Sciences, Xinjiang Production and Construction Corps Key Laboratory of Oasis Town and Mountain-basin System Ecology, Key Laboratory of Xinjiang Phytomedicine Resource Utilization, Shihezi University, Ministry of Education, North 4th Road, Xinjiang, Shihezi, 832003, China.
Zihan GuoCollege of life Sciences, Xinjiang Production and Construction Corps Key Laboratory of Oasis Town and Mountain-basin System Ecology, Key Laboratory of Xinjiang Phytomedicine Resource Utilization, Shihezi University, Ministry of Education, North 4th Road, Xinjiang, Shihezi, 832003, China.
Fengqi LuoCollege of life Sciences, Xinjiang Production and Construction Corps Key Laboratory of Oasis Town and Mountain-basin System Ecology, Key Laboratory of Xinjiang Phytomedicine Resource Utilization, Shihezi University, Ministry of Education, North 4th Road, Xinjiang, Shihezi, 832003, China.
Yan ZhangCrop Research Institute of Xinjiang Uygur Autonomous Region Academy of Agricultural Sciences, No. 403 Nanchang Road, Urumqi, Xinjiang, 830091, China. yyd19@cau.edu.cn.
Jie YanCollege of life Sciences, Xinjiang Production and Construction Corps Key Laboratory of Oasis Town and Mountain-basin System Ecology, Key Laboratory of Xinjiang Phytomedicine Resource Utilization, Shihezi University, Ministry of Education, North 4th Road, Xinjiang, Shihezi, 832003, China. jiey@shzu.edu.cn.

Funding

National Natural Science Foundation of China 31860070Tianshan Talent Training Program 2023TSYCLJ0010
6 · The paper itself

Abstract

Brassinosteroids (BRs), a class of plant sterol hormones, regulate both secondary metabolite production and plant growth and development. Taraxacum kok-saghyz (TKS), one of the most important rubber-producing plants, accumulates substantial natural rubber in its roots. The biosynthesis of natural rubber is modulated by plant hormones such as brassinosteroids and ethylene, yet the regulatory framework governing natural rubber production in TKS remains poorly understood. In this study, TKS was used as experimental material to examine the relationship between rubber yield and different concentrations of BR solution. Following treatment with the optimal BR concentration, plants were subjected to varying durations of exposure and analyzed using combined transcriptomic and metabolomic approaches. The results demonstrated that BR significantly increased rubber production in TKS. Maximum productivity was achieved at a BR concentration of 0.1 mg/L, which enhanced rubber yield by 22.4% compared to the CK group. Transcriptional analysis revealed that BR treatment triggered a dynamic transcriptional response in the rubber biosynthesis pathway. Key enzyme genes (including AACT, HMGR, HMGS, MVK, PK, CMK, DXS, REF, CPT, and SRPP) were initially significantly upregulated at early stages, followed by a subsequent downregulation and later upregulation for most of them, indicating a complex temporal pattern of pathway activation. Temporal metabolomic profiling revealed that BR enhance natural rubber biosynthesis in rubber grass by orchestrating a coordinated metabolic reprogramming. This process is characterized by the accumulation of key intermediates (e.g., 2-C-methyl-D-erythritol 4-phosphate and 3-Hydroxy-3-methylpentane-1,5-dioic acid) and the sequential bolstering of precursor supply, redox homeostasis, and energy provision. This metabolic evidence strongly supports the transcriptomic data indicating BR-mediated upregulation of the rubber synthesis pathway. This study advances our understanding of BR’s regulatory role in natural rubber biosynthesis and provides valuable experimental insights for improving rubber production in practical applications.

Indexed as

BrassinosteroidsMetabolomicsRubberTaraxacumTranscriptomeGene Expression ProfilingGene Expression Regulation, PlantBrassinosteroidsRubberBrassinosteroidsMetabolomeNatural rubberTaraxacum kok-saghyzTranscriptome

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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 Socratic graph.