ArticleBMC genomics2025
Whole-genome sequencing and analysis of the symbiotic Mycena sp. L02 with Gastrodia Elata.
Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
backgroundMycena is a widespread genus of mushroom capable of decomposing various dead plant substrates. Gastrodia elata is a fully mycoheterotrophic orchid whose seed germination depends on specific Mycena strains. However, only a few Mycena species are capable of inducing germination, necessitating the identification of novel germinating fungal resources.
resultsThe genome of Mycena sp. L02 was sequenced using the Illumina NovaSeq and Oxford Nanopore Technologies (ONT) platforms. The final assembly spanned 160.06 Mb, with 36,246 genes predicted and repetitive sequences accounting for 31.90% (46,496,154 bp) of the genome. A total of 1,339 CAZyme genes were annotated, along with 3,772 genes involved in host-pathogen interactions, 88.33% of which were associated with loss of pathogenicity, reduced virulence, or unaffected pathogenicity. Comparative genomic analysis between germinating and non-germinating Mycena strains revealed that their CAZymes and PHI gene characteristics represent common traits shared across the Mycena genus, with no distinctive features identified. Furthermore, pathways enriched in unique gene families of the germinating fungi-such as glutathione metabolism, sulfur metabolism, phosphatidylinositol signaling system, and inositol phosphate metabolism-may contribute to the germination of G. elata seeds.
conclusionsThe abundance of CAZymes and low-virulence genes in L02 ensures sufficient nutrient acquisition and may facilitate hyphal penetration of the lignin-rich seed coat of G. elata, thereby enabling successful symbiosis. Additionally, KEGG pathways enriched in the unique gene families of the germinating fungi may contribute to the stimulation of seed germination in G. elata. Overall, this study provides a valuable genomic foundation for screening high-performance germinating fungi and further investigating the molecular mechanisms underlying the symbiosis with G. elata.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.