Evidence map›Paper›PMID 40903900›Full record

ArticlePlant communications2025

Fungal symbiont Mycena complements impaired nitrogen utilization in Gastrodia elata and supplies indole-3-acetic acid to facilitate its seed germination.

Qing-Song Yuan, Lu Luo, Haixia Shi, Hui Wang, Jiuchun An, Yanping Gao, Jiao Xu, Xiaohong Ou, Ye Yang, Karim M Tabl and 3 more

Abstract read
In one paragraph

Article in Plant communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Orchid genome evolution and trait innovation.Journal of integrative plant biology · 2026
    Review
  2. Article
  3. Article
  4. IMA fungus · 2026
    Article
  5. 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.

Qing-Song YuanGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China; National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China; State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Beijing 100700, China. Electronic address: yqs198609031006@126.com.
Lu LuoGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China.
Haixia ShiGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China.
Hui WangGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China.
Jiuchun AnGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China.
Yanping GaoGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China.
Jiao XuGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China.
Xiaohong OuGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China.
Ye YangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan 650050, China.
Karim M TablAgricultural Botany Department, Faculty of Agriculture (Saba Basha), Alexandria University, Alexandria 21531, Egypt.
Lanping GuoNational Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China; State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Beijing 100700, China. Electronic address: glp01@126.com.
Luqi HuangNational Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China; State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Beijing 100700, China. Electronic address: huangluqi01@126.com.
Tao ZhouGuizhou University of Traditional Chinese Medicine, Guiyang, Guizhou 550025, China; Guizhou Key Laboratory for Germplasm Innovation and Resource-Efficient Utilization of Dao-di Herbs, Guiyang, Guizhou 550025, China. Electronic address: taozhou88@163.com.

Funding

Non-US Government Research Support type
6 · The paper itself

Abstract

Nitrogen and auxin uptake play pivotal roles in seed germination and development. Gastrodia elata, a fully mycoheterotrophic plant, depends entirely on its symbiotic association with Mycena for early growth and seed germination. The process by which Mycena supplies nitrogen nutrients and auxin, which are deficient in G. elata, remains poorly understood. In this study, genome-scale analysis of G. elata revealed the loss of genes associated with nitrogen utilization and indole-3-acetic acid (IAA) biosynthesis, which are retained in Mycena. Further analysis of the dynamic transcriptomic interactions between G. elata seeds and Mycena across different symbiotic stages revealed that genes involved in nitrogen- and tryptophan-dependent IAA biosynthesis were significantly upregulated in Mycena during the symbiotic germination of G. elata seeds. Concurrently, G. elata seeds exhibited increased expression of genes involved in the hormone signal transduction pathway and the starch and sucrose metabolism pathway. Functional disruption of nitrite reductase (MyNir, EVM0012344) and amidase (MyAmid, EVM0010270), key enzymes in nitrogen assimilation and IAA biosynthesis in Mycena, significantly impaired the symbiotic germination of G. elata seeds. This disruption interfered with energy supply, caused cellular restructuring, and altered hormonal signaling crosstalk. In conclusion, our findings provide novel insights into the mutualistic symbiotic relationship between Mycena and G. elata. Specifically, the fungus Mycena compensates for the incomplete nitrogen metabolism of its plant partner, G. elata, and supplies IAA, thereby promoting seed germination. These results shed light on plant-fungal symbiotic associations from the perspective of nitrogen utilization.

Indexed as

GastrodiaGerminationIndoleacetic AcidsNitrogenSymbiosisPlant Growth RegulatorsSeedsindoleacetic acidIndoleacetic AcidsNitrogenPlant Growth RegulatorsGastrodia elataindole-3-acetic acid biosynthesisMycenanitrogen utilizationsymbiotic germination

Identifiers

PMID40903900
PMCPMC12546762

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.