ArticleBMC genomics2025
Proteome study of dikaryotic and monokaryotic mycelia reveals the transfer between biological processes contributing to dikaryon growth advantage of the medicinal fungus Ganoderma lucidum.
Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Occupationally relevant vibrations and the brain: frequency-dependent proteomics signatures in a rat model.Annals of medicine · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
backgroundGanoderma lucidum, a well-known medicinal fungus in traditional Chinese medicine, exhibits a superior growth rate in its dikaryotic mycelia compared to monokaryons, and this is essential for its fruiting body formation and medicinal utilization. However, the biological process landscape contributing to the dikaryon growth advantage remains largely unexplored. This study performed Tandem Mass Tag (TMT)-based proteomic analysis of the dikaryotic mycelia and two compatible monokaryotic mycelia to elucidate the mechanism underlying this growth advantage.
resultsDikaryotic mycelia showed superior growth rates over monokaryons in both solid and liquid cultures. Proteomic analysis revealed a remodeled proteome of the dikaryon, with elevated expression levels of proteins involved in biosynthesis and processing of protein and RNA, cell structure, and cell division, compared to monokaryons, in both global proteins (3990) and differentially expressed proteins (983) analysis. In contrast, metabolism related proteins, particularly those involved in energy production and conversion, expressed at lower levels in dikaryon compared to monokaryons. Nonetheless, the energy-consuming proteins showed high expression in dikaryon.
conclusionsThese results indicate diverse remodeled biological processes coordinately contribute to the dikaryon growth advantage, especially the transfer from energy metabolism to biosynthesis and growth with high energy utilization efficiency. This is the first discovery of metabolic remodeling in dikaryotic mycelia of G. lucidum, presenting favorable implications for the breeding of G. lucidum.
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.