Development of a homologous transformation system for the human pathogenic fungus Aspergillus fumigatus based on the pyrG gene encoding orotidine 5′-monophosphate decarboxylase

被引:193
作者
Weidner, G
d'Enfert, C
Koch, A
Mol, PC
Brakhage, AA
机构
[1] Univ Munich, Lehrstuhl Mikrobiol, D-80638 Munchen, Germany
[2] Inst Pasteur, Lab Aspergillus, F-75724 Paris 15, France
关键词
Aspergillus fumigatus; DNA-mediated transformation; orotidine 5 '-monophosphate decarboxylase; electroporation;
D O I
10.1007/s002940050350
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A homologous transformation system for the opportunistic fungal pathogen Aspergillus fumigatus was developed. It is based on the A. fumigatus pyrG gene, encoding orotidine 5'-monophosphate decarboxylase, which was cloned and sequenced. Transformation of both Aspergillus (Emericella) nidulans and A. fumigatus pyrG mutant strains by the use of protoplasts or electroporation established the functionality of the cloned gene. DNA sequencing of the A. fumigatus pyrG1 mutant allele revealed that it encodes a truncated, non-functional, PyrG protein. Transformation of an A. fumigatus pyrG1 mutant with a plasmid carrying the novel pyrG2 allele constructed by in vitro mutagenesis yielded prototrophic transformants following recombination between both mutation sites. Analysis of transformants carrying the entire plasmid showed that up to 45% of integration had occurred at the pyrG locus. This provides a tool to target defined genetic constructs at a specific locus in the A. fumigatus genome in order to study gene regulation and function.
引用
收藏
页码:378 / 385
页数:8
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