Department of Biology, Niagara University, Niagara, NY, USA.
Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Methods Mol Biol. 2022;2542:91-99. doi: 10.1007/978-1-0716-2549-1_6.
Complex haploinsufficiency refers to the genetic interaction that occurs in strains with heterozygous mutations at two different loci (a double heterozygous deletion mutant). Double heterozygous deletion mutants can be used to identify gene partners that act within the same pathway or to determine expression-dependent genetic interactions that result in phenotypic changes outside of what would be expected based on the phenotypes of the single heterozygous deletion mutants. The approach outlined here uses a lithium acetate transformation method on a parental "query" strain to introduce a transcription factor deletion DNA construct that is derived from the Homann et al. Candida albicans transcription factor deletion library (Homann et al. PLoS Genet 5(12):e1000783, 2009). We also outline the steps to confirming the genotype of the resulting transformants as well as an example of the use of double heterozygous deletion mutants for complex haploinsufficiency analysis of biofilm formation.
复杂的单倍体不足是指在两个不同基因座(双杂合缺失突变体)存在杂合突变的菌株中发生的遗传相互作用。双杂合缺失突变体可用于鉴定在同一途径中起作用的基因伙伴,或确定导致表型变化的表达依赖性遗传相互作用,这些变化超出了基于单个杂合缺失突变体表型的预期。这里概述的方法在亲本“查询”菌株上使用锂乙酸盐转化方法,引入转录因子缺失 DNA 构建体,该构建体源自 Homann 等人的白色念珠菌转录因子缺失文库(Homann 等人,PLoS Genet 5(12):e1000783,2009 年)。我们还概述了确认转化子基因型的步骤,以及使用双杂合缺失突变体进行生物膜形成的复杂单倍体不足分析的示例。