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Published on: November 8, 2006
Protein O-mannosyltransferases B and C support hyphal development and differentiation in Aspergillus nidulans
Masatoshi Goto1, Yuka Harada, Takuji Oka
1Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, 6-10-1 Hakozaki, Fukuoka 812-8581, Japan. mgoto@brs.kyushu-u.ac.jp
Abstract:
Aspergillus nidulans possesses three pmt genes encoding protein O-d-mannosyltransferases (Pmt). Previously, we reported that PmtA, a member of the PMT2 subfamily, is involved in the proper maintenance of fungal morphology and formation of conidia (T. Oka, T. Hamaguchi, Y. Sameshima, M. Goto, and K. Furukawa, Microbiology 150:1973-1982, 2004). In the present paper, we describe the characterization of the pmtA paralogues pmtB and pmtC. PmtB and PmtC were classified as members of the PMT1 and PMT4 subfamilies, respectively. A pmtB disruptant showed wild-type (wt) colony formation at 30 degrees C but slightly repressed growth at 42 degrees C. Conidiation of the pmtB disruptant was reduced to approximately 50% of that of the wt strain; in addition, hyperbranching of hyphae indicated that PmtB is involved in polarity maintenance. A pmtA and pmtB double disruptant was viable but very slow growing, with morphological characteristics that were cumulative with respect to either single disruptant. Of the three single pmt mutants, the pmtC disruptant showed the highest growth repression; the hyphae were swollen and frequently branched, and the ability to form conidia under normal growth conditions was lost. Recovery from the aberrant hyphal structures occurred in the presence of osmotic stabilizer, implying that PmtC is responsible for the maintenance of cell wall integrity. Osmotic stabilization at 42 degrees C further enabled the pmtC disruptant to form conidiophores and conidia, but they were abnormal and much fewer than those of the wt strain. Apart from the different, abnormal phenotypes, the three pmt disruptants exhibited differences in their sensitivities to antifungal reagents, mannosylation activities, and glycoprotein profiles, indicating that PmtA, PmtB, and PmtC perform unique functions during cell growth.
Insights
Aspergillus nidulans protein O-d-mannosyltransferases (Pmt) A, B, and C have unique roles in fungal growth. Disrupting these genes affects morphology, cell wall integrity, and conidiation, highlighting their distinct functions.
Area of Science:
- * Mycology
- * Molecular Biology
- * Biochemistry
Background:
- * Aspergillus nidulans has three protein O-d-mannosyltransferase (Pmt) genes: pmtA, pmtB, and pmtC.
- * PmtA, a PMT2 subfamily member, is crucial for fungal morphology and conidia formation.
- * This study characterizes the paralogous genes pmtB (PMT1 subfamily) and pmtC (PMT4 subfamily).
Purpose of the Study:
- * To characterize the functions of pmtB and pmtC in Aspergillus nidulans.
- * To understand the specific roles of PmtA, PmtB, and PmtC in fungal development and cell wall integrity.
Main Methods:
- * Gene disruption of pmtB and pmtC in Aspergillus nidulans.
- * Phenotypic analysis of single and double disruptants at different temperatures (30°C and 42°C).
- * Assessment of growth, morphology, conidiation, cell wall integrity using osmotic stabilizers, and sensitivity to antifungal reagents.
Main Results:
- * pmtB disruptant showed reduced conidiation and hyphal hyperbranching, indicating a role in polarity maintenance.
- * pmtA and pmtB double disruptant exhibited cumulative growth defects.
- * pmtC disruptant displayed severe growth repression, swollen hyphae, and loss of conidiation, suggesting a role in cell wall integrity.
- * PmtC function was partially restored by osmotic stabilizers, especially at 42°C.
- * All three pmt disruptants showed unique sensitivities to antifungal agents and alterations in mannosylation and glycoproteins.
Conclusions:
- * PmtA, PmtB, and PmtC are essential for distinct cellular processes in Aspergillus nidulans.
- * PmtB is involved in polarity maintenance.
- * PmtC is critical for cell wall integrity.
- * The unique functions of these protein O-d-mannosyltransferases contribute to overall fungal cell growth and development.
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