ABSTRACT
A series of Neurospora crassa mutants affected in the ability to regulate entry into conidiation (an asexual developmental program) were isolated by using an insertional mutagenesis procedure followed by a screening protocol. One of the mutants isolated by this approach consisted entirely of cells with an abnormal morphology. The mutant produces chains of swollen septated cells. The developmentally regulated ccg-1 gene is constitutively expressed in these cells, suggesting that they have entered the conidial developmental program. The insertionally disrupted gene cnb-1 was isolated by plasmid rescue and found to encode calcineurin B, the regulatory subunit of the Ca2+ and calmodulin-dependent protein phosphatase calcineurin. The data demonstrate that calcineurin B is required for normal vegetative growth in N. crassa and suggest that the cnb-1 mutant is unable to repress entry into the asexual developmental program. The results suggest that Ca2+ may play an important role in regulating fungal morphology.
Subject(s)
Calcineurin/genetics , Calcineurin/metabolism , Neurospora crassa/growth & development , Amino Acid Sequence , Base Sequence , Calcineurin/chemistry , Gene Expression Regulation, Fungal , Molecular Sequence Data , Mutagenesis, Insertional , Neurospora crassa/genetics , Plasmids/genetics , Sequence Analysis, DNAABSTRACT
Using an insertional mutagenesis approach, a series of Neurospora crassa mutants affected in the ability to control entry into the conidiation developmental program were isolated. One such mutant, GTH16-T4, was found to lack normal vegetative hyphae and to undergo constitutive conidiation. The affected gene has been named nrc-1, for nonrepressible conidiation gene #1. The nrc-1 gene was cloned from the mutant genomic DNA by plasmid rescue, and was found to encode a protein closely related to the protein products of the Saccharomyces cerevisiae STE11 and Schizosaccharomyces pombe byr2 genes. Both of these genes encode MAPKK kinases that are necessary for sexual development in these organisms. We conclude the nrc-1 gene encodes a MAPKK kinase that functions to repress the onset of conidiation in N. crassa. A second mutant, GTH16-T17, was found to lack normal vegetative hyphae and to constitutively enter, but not complete, the conidiation program. The affected locus is referred to as nrc-2 (nonrepressible conidiation gene #2). The nrc-2 gene was cloned and found to encode a serine-threonine protein kinase. The kinase is closely related to the predicted protein products of the S. pombe kad5, and the S. cerevisiae YNRO47w and KIN82 genes, three genes that have been identified in genome sequencing projects. The N. crassa nrc-2 gene is the first member of this group of kinases for which a phenotype has been defined. We conclude a functional nrc-2-encoded serine/threonine kinase is required to repress entry into the conidiation program.