Isolation of UmRrm75, a gene involved in dimorphism and virulence of Ustilago maydis
Article
-
- Overview
-
- Research
-
- Identity
-
- Additional Document Info
-
- View All
-
Overview
abstract
-
Ustilago maydis displays dimorphic growth, alternating between a saprophytic haploid yeast form and a filamentous dikaryon, generated by mating of haploid cells and which is an obligate parasite. Induction of the dimorphic transition of haploid strains . in vitro by change in ambient pH has been used to understand the mechanisms governing this differentiation process. In this study we used suppression subtractive hybridization to generate a cDNA library of . U. maydis genes up-regulated in the filamentous form induced . in vitro at acid pH. Expression analysis using quantitative RT-PCR showed that the induction of two unigenes identified in this library coincided with the establishment of filamentous growth in the acid pH medium. This expression pattern suggested that they were specifically associated to hyphal development rather than merely acid pH-induced genes. One of these genes, . UmRrm75, encodes a protein containing three RNA recognition motifs and glycine-rich repeats and was selected for further study. The . UmRrm75 gene contains 4 introns, and produces a splicing variant by a 3%27-alternative splicing site within the third exon. Mutants deleted for . UmRrm75 showed a slower growth rate than wild type strains in liquid and solid media, and their colonies showed a donut-like morphology on solid medium. Interestingly, although Δ. UmRrm75 strains were not affected in filamentous growth induced by acid pH and oleic acid, they exhibited reduced mating, post-mating filamentous growth and virulence. Our data suggest that . UmRrm75 is probably involved in cell growth, morphogenesis, and pathogenicity in . U. maydis. © 2011 Elsevier GmbH.
-
Ustilago maydis displays dimorphic growth, alternating between a saprophytic haploid yeast form and a filamentous dikaryon, generated by mating of haploid cells and which is an obligate parasite. Induction of the dimorphic transition of haploid strains . in vitro by change in ambient pH has been used to understand the mechanisms governing this differentiation process. In this study we used suppression subtractive hybridization to generate a cDNA library of . U. maydis genes up-regulated in the filamentous form induced . in vitro at acid pH. Expression analysis using quantitative RT-PCR showed that the induction of two unigenes identified in this library coincided with the establishment of filamentous growth in the acid pH medium. This expression pattern suggested that they were specifically associated to hyphal development rather than merely acid pH-induced genes. One of these genes, . UmRrm75, encodes a protein containing three RNA recognition motifs and glycine-rich repeats and was selected for further study. The . UmRrm75 gene contains 4 introns, and produces a splicing variant by a 3'-alternative splicing site within the third exon. Mutants deleted for . UmRrm75 showed a slower growth rate than wild type strains in liquid and solid media, and their colonies showed a donut-like morphology on solid medium. Interestingly, although Δ. UmRrm75 strains were not affected in filamentous growth induced by acid pH and oleic acid, they exhibited reduced mating, post-mating filamentous growth and virulence. Our data suggest that . UmRrm75 is probably involved in cell growth, morphogenesis, and pathogenicity in . U. maydis. © 2011 Elsevier GmbH.
publication date
published in
Research
keywords
-
Dimorphism; Donut-like shape colony; Pathogenicity; RNA binding protein; Subtractive library; Ustilago maydis Dimorphism; Donut-like shape colony; Pathogenicity; RNA binding protein; Subtractive library; Ustilago maydis; Amino acids; Oleic acid; Polymerase chain reaction; RNA; Gene expression; fungal protein; RNA binding protein; colony; dimorphism; fungal disease; fungus; gene; growth rate; pathogen; pathogenicity; pH; polymerase chain reaction; protein; real time; virulence; amino acid sequence; article; chemistry; fungal gene; fungus hyphae; gene expression regulation; genetics; growth, development and aging; maize; metabolism; microbiology; molecular genetics; pathogenicity; plant disease; protein motif; sequence alignment; Ustilago; virulence; Amino Acid Motifs; Amino Acid Sequence; Fungal Proteins; Gene Expression Regulation, Fungal; Genes, Mating Type, Fungal; Hyphae; Molecular Sequence Data; Plant Diseases; RNA-Binding Proteins; Sequence Alignment; Ustilago; Virulence; Zea mays; Ustilago maydis
Identity
Digital Object Identifier (DOI)
PubMed ID
Additional Document Info
start page
end page
volume
issue