Abstract

Genome sequencing of Tricholoma matsutake revealed its unusually large size as 189.0 Mbp, which is a consequence of extraordinarily high transposable element (TE) content. We identified that 702 genes were surrounded by TEs, and 83.2% of these genes were not transcribed at any developmental stage. This observation indicated that the insertion of TEs alters the transcription of the genes neighboring these TEs. Repeat-induced point mutation, such as C to T hypermutation with a bias over “CpG” dinucleotides, was also recognized in this genome, representing a typical defense mechanism against TEs during evolution. Many transcription factor genes were activated in both the primordia and fruiting body stages, which indicates that many regulatory processes are shared during the developmental stages. Small secreted protein genes (<300 aa) were dominantly transcribed in the hyphae, where symbiotic interactions occur with the hosts. Comparative analysis with 37 Agaricomycetes genomes revealed that IstB-like domains (PF01695) were conserved across taxonomically diverse mycorrhizal genomes, where the T. matsutake genome contained four copies of this domain. Three of the IstB-like genes were overexpressed in the hyphae. Similar to other ectomycorrhizal genomes, the CAZyme gene set was reduced in T. matsutake, including losses in the glycoside hydrolase genes. The T. matsutake genome sequence provides insight into the causes and consequences of genome size inflation.

Highlights

  • Tricholoma matsutake is an ectomycorrhizal (ECM) basidiomycete that establishes a symbiotic relationship with the roots of Pinus densiflora, giving it the name “pine mushroom” [1]

  • Despite a previous report that states that repeat-induced point mutation (RIP) does not exist in Agaricomycotina genomes [20], we identified the pattern of CpG hypermutations in the genome, further studies remain to reveal whether the actual RIP process made this pattern (Fig D in S1 File)

  • TMHMM 2.0 [57] was used with default options, and when a transmembrane helix was located within 70 aa of the N-terminal and other helixes were not identified, we considered this as a non-transmembrane protein, with reference to previous work [58]

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Summary

Objectives

This study aimed to explore the genome composition of ectomycorrhizal Tricholoma matsutake

Methods
Results
Conclusion
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