Cross-talk between Tor1 and Sch9 regulates hyphae-specific genes or ribosomal protein genes in a mutually exclusive manner in Candida albicans

Se Woong Kim, Yoo Jin Joo, Yu Jin Chun, Young Kwang Park, Joon Kim

Research output: Contribution to journalArticle

Abstract

The human fungal pathogen Candida albicans switches its morphology from yeast to hyphal forms. The morphological transition may render C. albicans virulent. Several signaling cascades, including those of the cyclic AMP-protein kinase A and mitogen-activated protein kinase pathways, are responsible for morphogenesis. In this study, we observed a reduction in gene transcription of ribosomal proteins during true hyphae formation. Moreover, morphogenesis-dependent decrease in ribosomal protein gene transcription was confirmed in constitutive yeast or filamentous growing strains. We consistently observed that polysome and monosome levels were decreased by hyphal stimuli through TORC1 and Sch9 kinases. Taken together, these results provide several lines of evidence to show that the Tor1–Sch9 kinase cascade, which stimulates transcription of ribosomal protein genes, exists in C. albicans. Thus, the present study revealed a novel link between ribosome biogenesis and morphogenesis in C. albicans that is mediated by Tor1 and Sch9.

Original languageEnglish
Pages (from-to)1041-1057
Number of pages17
JournalMolecular Microbiology
Volume112
Issue number3
DOIs
Publication statusPublished - 2019 Sep 1

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Hyphae
Ribosomal Proteins
Candida albicans
Morphogenesis
Genes
Proteins
Phosphotransferases
Yeasts
Adenylate Kinase
Polyribosomes
Cyclic AMP-Dependent Protein Kinases
Mitogen-Activated Protein Kinases
Ribosomes
Cyclic AMP

ASJC Scopus subject areas

  • Microbiology
  • Molecular Biology

Cite this

Cross-talk between Tor1 and Sch9 regulates hyphae-specific genes or ribosomal protein genes in a mutually exclusive manner in Candida albicans. / Kim, Se Woong; Joo, Yoo Jin; Chun, Yu Jin; Park, Young Kwang; Kim, Joon.

In: Molecular Microbiology, Vol. 112, No. 3, 01.09.2019, p. 1041-1057.

Research output: Contribution to journalArticle

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