Zemska Olga, Rappleye Chad A
Department of Microbiology, Ohio State University, Columbus, OH, USA.
Methods Mol Biol. 2012;845:51-66. doi: 10.1007/978-1-61779-539-8_4.
Genome-wide mutagenesis is a powerful method for identifying new genes that contribute to a phenotype of interest. For many fungal pathogens of plants and animals, Agrobacterium tumefaciens-mediated transformation (ATMT) serves as an efficient insertional mutagen. In Histoplasma capsulatum, the T-DNA element transferred by Agrobacterium stably integrates into the genome, and the majority of mutants contain single copies of the inserted sequence. The T-DNA sequence facilitates the determination of the genomic sequence flanking the insertion through hemi-specific PCR techniques, plasmid rescue, or inverse PCR. We present optimized procedures for generating insertional mutants in H. capsulatum using Agrobacterium-mediated transformation and using this for forward and reverse genetic approaches.
全基因组诱变是鉴定导致感兴趣表型的新基因的有力方法。对于许多动植物的真菌病原体而言,根癌农杆菌介导的转化(ATMT)是一种有效的插入诱变方法。在荚膜组织胞浆菌中,农杆菌转移的T-DNA元件稳定整合到基因组中,并且大多数突变体包含插入序列的单拷贝。T-DNA序列有助于通过半特异性PCR技术、质粒拯救或反向PCR来确定插入侧翼的基因组序列。我们展示了使用农杆菌介导的转化在荚膜组织胞浆菌中产生插入突变体并将其用于正向和反向遗传方法的优化程序。