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The WOPR Domain Protein OsaA Orchestrates Development in Aspergillus nidulans
Author(s) -
Alkahyyat Fahad,
Min Ni,
Sun Chang Kim,
JaeHyuk Yu
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0137554
Subject(s) - aspergillus nidulans , biology , mutant , phenotype , conidiation , genetics , transcriptome , microbiology and biotechnology , gene , protein domain , gene expression
Orchestration of cellular growth and development occurs during the life cycle of Aspergillus nidulans . A multi-copy genetic screen intended to unveil novel regulators of development identified the AN6578 locus predicted to encode a protein with the WOPR domain, which is a broadly present fungi-specific DNA-binding motif. Multi-copy of AN6578 disrupted the normal life cycle of the fungus leading to enhanced proliferation of vegetative cells, whereas the deletion resulted in hyper-active sexual fruiting with reduced asexual development (conidiation), thus named as osaA ( O rchestrator of S ex and A sex). Further genetic studies indicate that OsaA balances development mainly by repressing sexual development downstream of the velvet regulator VeA. The absence of osaA is sufficient to suppress the veA1 allele leading to the sporulation levels comparable to veA + wild type (WT). Genome-wide transcriptomic analyses of WT, veA1 , and Δ osaA veA1 strains by RNA-Seq further corroborate that OsaA functions in repressing sexual development downstream of VeA. However, OsaA also plays additional roles in controlling development, as the Δ osaA veA1 mutant exhibits precocious and enhanced formation of Hülle cells compared to WT. The OsaA orthologue of Aspergillus flavus is able to complement the osaA null phenotype in A . nidulans , suggesting a conserved role of this group of WOPR domain proteins. In summary, OsaA is an upstream orchestrator of morphological and chemical development in Aspergillus that functions downstream of VeA.

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