Transcriptome analysis and its application in identifying genes associated with fruiting body development in basidiomycete Hypsizygus marmoreus

PLoS One. 2015 Apr 2;10(4):e0123025. doi: 10.1371/journal.pone.0123025. eCollection 2015.

Abstract

To elucidate the mechanisms of fruit body development in H. marmoreus, a total of 43609521 high-quality RNA-seq reads were obtained from four developmental stages, including the mycelial knot (H-M), mycelial pigmentation (H-V), primordium (H-P) and fruiting body (H-F) stages. These reads were assembled to obtain 40568 unigenes with an average length of 1074 bp. A total of 26800 (66.06%) unigenes were annotated and analyzed with the Kyoto Encyclopedia of Genes and Genomes (KEGG), Gene Ontology (GO), and Eukaryotic Orthologous Group (KOG) databases. Differentially expressed genes (DEGs) from the four transcriptomes were analyzed. The KEGG enrichment analysis revealed that the mycelium pigmentation stage was associated with the MAPK, cAMP, and blue light signal transduction pathways. In addition, expression of the two-component system members changed with the transition from H-M to H-V, suggesting that light affected the expression of genes related to fruit body initiation in H. marmoreus. During the transition from H-V to H-P, stress signals associated with MAPK, cAMP and ROS signals might be the most important inducers. Our data suggested that nitrogen starvation might be one of the most important factors in promoting fruit body maturation, and nitrogen metabolism and mTOR signaling pathway were associated with this process. In addition, 30 genes of interest were analyzed by quantitative real-time PCR to verify their expression profiles at the four developmental stages. This study advances our understanding of the molecular mechanism of fruiting body development in H. marmoreus by identifying a wealth of new genes that may play important roles in mushroom morphogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agaricales / genetics
  • Agaricales / growth & development*
  • Base Sequence
  • Cryptochromes / genetics
  • Cryptochromes / metabolism
  • Cyclic AMP / genetics
  • Cyclic AMP / metabolism
  • DNA, Fungal / genetics
  • Fruiting Bodies, Fungal / genetics
  • Fruiting Bodies, Fungal / growth & development*
  • Gene Expression Profiling
  • Gene Expression Regulation, Plant
  • Mitogen-Activated Protein Kinases / genetics
  • Mitogen-Activated Protein Kinases / metabolism
  • Molecular Sequence Data
  • Mycelium / growth & development*
  • Nitrogen / metabolism*
  • Pigmentation / genetics
  • Reactive Oxygen Species / metabolism
  • Sequence Analysis, DNA
  • Signal Transduction / genetics*
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Cryptochromes
  • DNA, Fungal
  • Reactive Oxygen Species
  • Cyclic AMP
  • TOR Serine-Threonine Kinases
  • Mitogen-Activated Protein Kinases
  • Nitrogen

Associated data

  • GENBANK/GBCL00000000
  • SRA/SRP040755

Grants and funding

This work was supported by the National Natural Science Foundation of China (Project No. 31401932) and the Key Scientific Research Project of Shanghai (Project No. 11391901003). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.