Oakley C Elizabeth, Edgerton-Morgan Heather, Oakley Berl R
Department of Molecular Biosciences, University of Kansas, Lawrence, KS, USA.
Methods Mol Biol. 2012;944:143-61. doi: 10.1007/978-1-62703-122-6_10.
Targeted gene deletions and promoter replacements are proving to be a valuable tool for awakening and analyzing silent secondary metabolism gene clusters in Aspergillus nidulans and, as molecular genetic methods for manipulating the genomes of other fungi are developed, they will likely be as valuable in those organisms. Here we describe procedures for constructing DNA fragments by PCR that can be used to replace genes or promoters quickly and on a large scale. We also describe transformation procedures for A. nidulans that allow these fragments to be introduced into target strains efficiently such that many genes or promoters can be replaced in a single experiment.
靶向基因缺失和启动子替换已被证明是激活和分析构巢曲霉中沉默次生代谢基因簇的一种有价值的工具,并且随着用于操纵其他真菌基因组的分子遗传学方法的发展,它们在这些生物体中可能同样有价值。在此,我们描述了通过PCR构建DNA片段的程序,这些片段可用于快速且大规模地替换基因或启动子。我们还描述了构巢曲霉的转化程序,该程序可使这些片段高效地导入目标菌株,从而在单个实验中可以替换许多基因或启动子。