Several genes have been identied that are highly expressed during conidiation. Inactivation ofthese genes has no observable phenotypic effect. Transcripts of two such genes, con-6 and con-10, are norally absent from vegetative mycella. To identify regulatory genes that affect con-6 and/or con-10 expression, strains were prepared in which the regulatory regions for these genes were fused to a gene conferrin hygromycin resistance. Mutants were then selected that were resistant to the drug during mycelial growth. Mutations in several of the isolates had trans effects; they activated transcription of the corresponding intact gene and, in most oates, one or more ofthe other con genes. Most Analyses of the protein and mRNA species present in mycelia, aerial hyphae, and conidia have revealed significant differences in gene expression (3)(4)(5). A differential screening procedure was used to clone genes that are preferentially expressed during conidiation (4). Four of these genes, con-6, con-8, con-10, and con-13, have been sequenced, and their expression has been examined (6-10). A fifth conidiationspecific gene, eas, also has been characterized (11, 12); eas encodes the rodlet protein that coats the surface ofthe mature conidium.con-6 and con-10 encode 93-and 86-residue polypeptides, respectively; the functions of these polypeptides are unknown. con-6 and con-10 transcripts and proteins are normally undetectable in vegetative mycelium but appear at high levels during conidiation and in mature conidia; these transcripts and proteins disappear a few hours after conidia germinate (6,13). The expression pattern of these genes closely parallels that of eas (11, 12). The con-6 and con-10 proteins are present in a second type of asexual spore, the microconidium (10,13), and the con-10 protein is present in sexual spores (10, 13). Expression of con-6 and con-10 can also be induced in vegetative mycelial cultures by light exposure or by imposing conditions that induce circadian rhythm (10,(13)(14)(15). We describe here the selection and partial characterization of mutants that express con-6 and con-10 aberrantly during vegetative mycelial growth. Some of these mutants were found to be blocked in conidiation, whereas others exhibited different developmental abnormalities.
MATERIALS AND METHODSStrains and Pids. Strain CH10 was constructed by homologous integration, using pCH10, a plasmid containing a con-10 translational fusion to the hygromycin phosphotransferase gene (hph) (16). Integration was at the his-3 locus of Fungal Genetics Stock Center (FGSC) strain 462: his-3 A. The integrated plasmid consisted of pBluescript KS+ (Promega) vector containing con-10 DNA from positions 1139 to 1935 (8); this segment contains the first 40 codons of con-10. The con-10 DNA is fused in-frame to the second codon of hph followed by the Aspergillus nidulans trpC transcription termination region from plasmid pDH25 (16). The plasmid also contains a 5' truncated copy of the his-3 gene that allows reconstitution of an intact copy of the ...