The Slt2-MAPK pathway is involved in the mechanism by which target of rapamycin regulates cell wall components in Ganoderma lucidum

Fungal Genet Biol. 2019 Feb:123:70-77. doi: 10.1016/j.fgb.2018.12.005. Epub 2018 Dec 14.

Abstract

The fungal cell wall is very important for cell growth and survival during stress, and the target of rapamycin (TOR) pathway plays a major role in regulating cell growth in response to environmental cues. Ganoderma lucidum is an important edible and medicinal fungus, and the function of TOR in this organism remains unclear. As shown in the present study, the TOR pathway regulates cell wall integrity (CWI) in G. lucidum. Inhibition of TOR signaling by RNA interference (RNAi) or rapamycin treatment reduced the growth of G. lucidum mycelia, increased contents of the cell wall components chitin and β-1,3-glucan, and increased cell wall thickness. Furthermore, inhibition of TOR signaling enhanced the relative level of phosphorylated Slt2, a member of the MAPK cascade involved in CWI signaling. Moreover, when treated with rapamycin, significantly lower chitin and β-1,3-glucan contents were observed in Slt2-silenced strains than in WT strains, indicating that TOR regulates the synthesis of these cell wall components through the Slt2-MAPK pathway. These results indicate a potential relationship between TOR signaling and CWI signaling. Additionally, participation of Slt2-MAPK in TOR-mediated regulation of cell wall component production has not previously been reported in a microorganism.

Keywords: Cell wall integrity; Ganoderma lucidum; Slt2-MAPK; TOR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Wall / genetics
  • Cell Wall / metabolism*
  • Chitin / chemistry
  • Chitin / genetics
  • MAP Kinase Signaling System / genetics
  • Mitogen-Activated Protein Kinases / chemistry
  • Mitogen-Activated Protein Kinases / genetics
  • Phosphorylation
  • RNA Interference
  • Reishi / genetics*
  • Reishi / metabolism
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins / chemistry
  • Saccharomyces cerevisiae Proteins / genetics
  • Sirolimus / metabolism*
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism*
  • beta-Glucans / chemistry

Substances

  • Saccharomyces cerevisiae Proteins
  • beta-Glucans
  • Chitin
  • beta-1,3-glucan
  • TOR Serine-Threonine Kinases
  • Mitogen-Activated Protein Kinases
  • SLT2 protein, S cerevisiae
  • Sirolimus