FlbD, a Myb Transcription Factor of Aspergillus nidulans, Is Uniquely Involved in both Asexual and Sexual Differentiation
Author(s) -
Jenny Arratia-Quijada,
Olivia Sánchez,
Claudio Scazzocchio,
Jesús Aguirre
Publication year - 2012
Publication title -
eukaryotic cell
Language(s) - English
Resource type - Journals
eISSN - 1535-9778
pISSN - 1535-9786
DOI - 10.1128/ec.00101-12
Subject(s) - conidiation , aspergillus nidulans , biology , mutant , genetics , gene , transcription factor , fungal protein , sexual reproduction , microbiology and biotechnology , phenotype
In the fungusAspergillus nidulans , inactivation of theflbA to-E ,fluG ,fluF , andtmpA genes results in similar phenotypes, characterized by a delay in conidiophore and asexual spore production.flbB to-D encode transcription factors needed for proper expression of thebrlA gene, which is essential for asexual development. However, recent evidence indicates that FlbB and FlbE also have nontranscriptional functions. Here we show thatfluF1 is an allele offlbD which results in an R47P substitution. Amino acids C46 and R47 are highly conserved in FlbD and many other Myb proteins, and C46 has been proposed to mediate redox regulation. Comparison of ΔflbD andflbD R47P mutants uncovered a new and specific role forflbD during sexual development. WhileflbD R47P mutants retain partial function during conidiation, bothΔflbD andflbD R47P mutants are unable to develop the peridium, a specialized external tissue that differentiates during fruiting body formation and ends up surrounding the sexual spores. This function, unique among otherfluffy genes, does not affect the viability of the naked ascospores produced by mutant strains. Notably, ascospore development in these mutants is still dependent on the NADPH oxidase NoxA. We generated R47K, C46D, C46S, and C46A mutant alleles and evaluated their effects on asexual and sexual development. Conidiation defects were most severe inΔflbD mutants and stronger in R47P, C46D, and C46S strains than in R47K strains. In contrast, mutants carrying theflbD C46A allele exhibited conidiation defects in liquid culture only under nitrogen starvation conditions. The R47K, R47P, C46D, and C46S mutants failed to develop any peridial tissue, while theflbD C46A strain showed normal peridium development and increased cleistothecium formation. Our results show that FlbD regulates both asexual and sexual differentiation, suggesting that both processes require FlbD DNA binding activity and that FlbD is involved in the response to nitrogen starvation.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom