The bZIP-type transcription factor FlbB regulates distinct morphogenetic stages of colony formation in Aspergillus nidulans

Mol Microbiol. 2009 Sep;73(5):775-89. doi: 10.1111/j.1365-2958.2009.06804.x. Epub 2009 Jul 28.

Abstract

Conidiophore formation in Aspergillus nidulans involves a developmental programme in which vegetative hyphae give rise to an ordered succession of differentiated cells: foot cell, stalk, vesicle, metulae, phialides and conidia. The developmental transition requires factors that are expressed in vegetative hyphae that activate the expression of the main regulator of conidiation, BrlA. One such element is the bZIP-type transcription factor FlbB. We found that flbB(-) mutants show defective branching patterns and are susceptible to autolysis under high sorbitol or sucrose concentrations, revealing a role in vegetative growth. In addition, FlbB plays a role in conidiophore initiation, as its upregulation reduces conidiophore vesicle swelling and generates a reduced number of metulae. FlbB was located at the tip of growing metulae, following a similar pattern as described in vegetative hyphae. In wild-type strains, the transition from metulae to phialides could be reversed to generate vegetative hyphae, indicating the existence of a specific control point at this stage of conidiophore formation. The combined evidence points to FlbB as a key factor in the transition to asexual development, playing a role at various control points in which the process could be reversed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Aspergillus nidulans / chemistry
  • Aspergillus nidulans / growth & development
  • Aspergillus nidulans / physiology*
  • Fungal Proteins / genetics
  • Fungal Proteins / physiology
  • Gene Deletion
  • Gene Expression Regulation, Fungal*
  • Hyphae / chemistry
  • Hyphae / physiology
  • Molecular Sequence Data
  • Sequence Alignment
  • Signal Transduction*
  • Spores, Fungal / growth & development*
  • Transcription Factors / genetics
  • Transcription Factors / physiology*

Substances

  • Fungal Proteins
  • Transcription Factors