Candida albicans VAC8 is required for vacuolar inheritance and normal hyphal branching

Caroline Barelle, Mathias L Richard, Claude Gaillardin, Neil A R Gow, Alistair J P Brown

Research output: Contribution to journalArticlepeer-review

27 Citations (Scopus)

Abstract

Hyphal growth is prevalent during most Candida albicans infections. Current cell division models, which are based on cytological analyses of C. albicans, predict that hyphal branching is intimately linked with vacuolar inheritance in this fungus. Here we report the molecular validation of this model, showing that a specific mutation that disrupts vacuolar inheritance also affects hyphal division. The armadillo repeat-containing protein Vac8p plays an important role in vacuolar inheritance in Saccharomyces cerevisiae. The VAC8 gene was identified in the C. albicans genome sequence and was resequenced. Homozygous C. albicans vac8Delta deletion mutants were generated, and their phenotypes were examined. Mutant vac8Delta cells contained fragmented vacuoles, and minimal vacuolar material was inherited by daughter cells in hyphal or budding forms. Normal rates of growth and hyphal extension were observed for the mutant hyphae on solid serum-containing medium. However, branching frequencies were significantly increased in the mutant hyphae. These observations are consistent with a causal relationship between vacuolar inheritance and the cell division cycle in the subapical compartments of C. albicans hyphae. The data support the hypothesis that cytoplasmic volume, rather than cell size, is critical for progression through G1.
Original languageEnglish
Pages (from-to)359-367
Number of pages9
JournalEukaryotic Cell
Volume5
Issue number2
DOIs
Publication statusPublished - Feb 2006

Keywords

  • amino acid sequence
  • candida albicans
  • fungal proteins
  • gene deletion
  • hyphae
  • molecular sequence data
  • phenotype
  • vacuoles
  • yeast candida-albicans
  • saccharomyces cerevisiae
  • cell-cycle
  • molecular analysis
  • protein
  • segregation
  • gene
  • fusion
  • morphology
  • mutants

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