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Shiitake, Hua Gu · 2025 · Preprint

High relevance

The alterations of the synthetic pathway and metabolic flux of auxin indole-3-acetic acid (IAA) govern thermotolerance in Lentinula edodes mycelia subjected to heat stress

Lentinula edodes

Energy & fatigueMetabolic healthLiver support
SpeciesShiitake, Hua Gu
JournalNot listed
Year2025

Key points

  • ABSTRACT Heat stress poses a significant constraint on the annual production of Lentinula edodes(L. edodes), a challenge that has been intensified by global warming
  • Previous studies have established a close relationship between intracellular indole-3-acetic acid (IAA) content and heat tolerance in L. edodes
  • Our findings revealed that IAA is primarily synthesized via the tryptamine (TAM) and indole-3-pyruvic acid (IPYA) pathways in L. edodes
  • Silencing of the key genes of IAA synthesis include tryptophan decarboxylase (TDC) and tryptophan transaminase (TAA) in strain S606 could reduce the thermotolerance of L. edodes mycelia
  • Transcriptome analysis revealed that heat-tolerant strain S606 had an earlier response to protein folding and mitochondrial gene expression compared to the heat-sensitive strain Y3357
  • Additionally, most genes in the MAPK signaling pathway were up-regulated after 10-24 hours of heat stress, with auxin response elements (AREs) identified in their promoters

From the paper

Abstract

ABSTRACT Heat stress poses a significant constraint on the annual production of Lentinula edodes(L. edodes), a challenge that has been intensified by global warming. Previous studies have established a close relationship between intracellular indole-3-acetic acid (IAA) content and heat tolerance in L. edodes. However, the specific changes in the IAA synthesis pathway and the target genes regulated by IAA under heat stress remain unclear. We employed targeted metabolomics and transcriptomics analysis to investigate the alterations in IAA synthesis pathways and gene expression in both heat-tolerant and heat-sensitive strains at various time points during heat stress. Our findings revealed that IAA is primarily synthesized via the tryptamine (TAM) and indole-3-pyruvic acid (IPYA) pathways in L. edodes. Heat-sensitive strain Y3357 exhibited excessive accumulation of tryptamine after heat stress. Silencing of the key genes of IAA synthesis include tryptophan decarboxylase (TDC) and tryptophan transaminase (TAA) in strain S606 could reduce the thermotolerance of L. edodes mycelia. Transcriptome analysis revealed that heat-tolerant strain S606 had an earlier response to protein folding and mitochondrial gene expression compared to the heat-sensitive strain Y3357. Additionally, most genes in the MAPK signaling pathway were up-regulated after 10-24 hours of heat stress, with auxin response elements (AREs) identified in their promoters. These results suggest that the excessive tryptamine accumulation is the newly discovered limiting factor for thermotolerance, and the expression levels of key genes in the IAA synthesis pathway could directly influence hyphal thermotolerance. This study provides a new perspective on the mechanism by which IAA and the synthesis precursors affects thermotolerance of L. edodes. Importance As an important plant hormone, the potential role of IAA in enhancing the heat resistance of L. edodes strains has garnered significant attention. This study systematically investigated the intracellular IAA biosynthesis pathway and its metabolic flows in L. edodes under varying durations of thermal stress, with particular emphasis on temporal gene expression patterns. Research has demonstrated that excessive accumulation of tryptamine may impair the heat stress recovery capability of L. edodes. In contrast, IAA can improve its thermotolerance by modulating the expression of genes associated with the MAPK signaling pathway.

Citation

Wei X, Song J, Chen J, Xiao Y, Zhou Y, Bian Y, et al. (2025). The alterations of the synthetic pathway and metabolic flux of auxin indole-3-acetic acid (IAA) govern thermotolerance in Lentinula edodes mycelia subjected to heat stress. https://doi.org/10.1101/2025.04.09.648085

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