Evidence map›Paper›PMID 41151625›Full record

ArticleJournal of advanced research2026

Physiological and multi-omics insights into ultraviolet B-induced stress adaptation in Fritillaria cirrhosa native to the Qinghai-Tibet Plateau.

Zemin Yang, Dan Gao, Ye Wang, Haitao Liu, Yuhan Wu, Haobo Zhang, Haiqing Wang, Xusheng Gao, Jialu Wang, Yonggang Wang and 3 more

Abstract read
In one paragraph

Article in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
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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

13 authors.

Zemin YangState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China; State Key Laboratory of Phytochemistry and Natural Medicines, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China. Electronic address: yangzm0615@163.com.
Dan GaoState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China. Electronic address: dgao@icmm.ac.cn.
Ye WangInstitute of Traditional Chinese Medicine Health Industry, China Academy of Chinese Medical Sciences, Nanchang 330115, China. Electronic address: ywang@itcmhi.ac.cn.
Haitao LiuInstitute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China. Electronic address: htliu@implad.ac.cn.
Yuhan WuState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China; College of Chinese Medicinal Materials, Jilin Agricultural University, Changchun 130118, China. Electronic address: wuyuhan13331615174@163.com.
Haobo ZhangState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China; College of Chinese Medicinal Materials, Jilin Agricultural University, Changchun 130118, China. Electronic address: zhanghb9810@163.com.
Haiqing WangNin Jiom Medicine Manufactory (Hong Kong) Limited, Hong Kong 999077, China. Electronic address: wanghaiqing0320@163.com.
Xusheng GaoCollege of Chinese Medicinal Materials, Jilin Agricultural University, Changchun 130118, China. Electronic address: gaoxusheng@o.cnu.ac.kr.
Jialu WangState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China. Electronic address: jialumarco2019@outlook.com.
Yonggang WangSchool of Life Science and Engineering, Lanzhou University of Technology, Lanzhou 730050, China. Electronic address: 412316788@163.com.
Huigan XieNin Jiom Medicine Manufactory (Hong Kong) Limited, Hong Kong 999077, China. Electronic address: kathytse@ninjiom.com.
Shaobing FuNin Jiom Medicine Manufactory (Hong Kong) Limited, Hong Kong 999077, China. Electronic address: bell.fu@163.com.
Xiwen LiState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China; Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China. Electronic address: xwli@icmm.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFritillaria cirrhosa (Liliaceae), an endangered medicinal plant of the Qinghai-Tibet Plateau, exhibits strong adaptability to ultraviolet B (UV-B) radiation during the transition from wild to artificial habitats. However, the molecular and physiological mechanisms underlying these adaptive responses remain largely unexplored, which hinders efforts to enhance their conservation and cultivation.

objectivesThe aim of this study was to comprehensively examine the morphological, cellular, and physiological responses of cultivated F. cirrhosa to UV-B radiation, with a particular focus on uncovering the key defense mechanisms that confer enhanced plant resilience.

methodsTo simulate its native high-altitude habitat, we augmented the growing area with ultraviolet radiation. Wild type F. cirrhosa was used as a control to systematically evaluate the response of cultivated plants to UV-B radiation, focusing on their morphology, cytology, and physiology. Multi-omics analyses were employed to uncover the transcriptional regulatory networks governing the responses of cultivated plants to UV-B stress.

resultsUV-B radiation induced substantial microstructural damage to the leaf mesophyll, chloroplasts, and stomatal complexes in both wild type and cultivated F. cirrhosa. However, the cultivated type exhibited significantly enhanced ability to maintain reactive oxygen species (ROS) homeostasis, effectively activating the antioxidant defense system and promoting the biosynthesis of UV-absorbing metabolites-thereby ensuring superior photosynthetic performance under UV-B stress. Mechanistically, upon UV-B detection, UVR8 photoreceptors in cultivated F. cirrhosa rapidly interact with the light regulatory protein COP1, forming the UVR8-COP1 complex, which stabilizes the light-signal transcription factor HY5 and modulates the activity of the FcMYB and FcWRKY transcription factors. This regulatory cascade promotes the biosynthesis of flavonoids and lignin, enhancing the transcription of key genes, namely FcPAL, Fc4CL, FcC4H, FcCHS, and FcF3H. This results in the accumulation of key phenolic compounds (xanthohumol, chrysin, luteolin, galangin, and pinocembrin) that function as "sunscreens" and "ROS scavengers", thereby effectively reducing UV-B-induced oxidative stress.

conclusionCompared to the wild type F. cirrhosa, the cultivated type demonstrated heightened UV-B tolerance through the activation of the UVR8-COP1-HY5 signaling pathway and increased biosynthesis of phenolic compounds. These insights provide a strong foundation for breeding strategies and conservation efforts to safeguard this valuable highland species.

Indexed as

Adaptation, PhysiologicalFritillariaStress, PhysiologicalUltraviolet RaysGene Expression Regulation, PlantPlant LeavesReactive Oxygen SpeciesTibetReactive Oxygen SpeciesAdaptive evolutionBiosynthetic pathwayFritillaria cirrhosaTranscriptional regulationTransgenerational stress memory

Identifiers

PMID41151625
PMCPMC13316609

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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.