Canela H M S, Takami L A, Ferreira M E S
Departamento de Ciências Farmacêuticas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.
Departamento de Ciências Farmacêuticas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil
Genet Mol Res. 2017 Feb 8;16(1):gmr-16-01-gmr.16019583. doi: 10.4238/gmr16019583.
Invasive aspergillosis is a disease responsible for high mortality rates, caused mainly by Aspergillus fumigatus. The available drugs are limited and this disease continues to occur at an unacceptable frequency. Gene disruption is essential in the search for new drug targets. An efficient protocol for A. fumigatus gene disruption was described but it requires ethidium bromide, a genotoxic agent, for DNA staining. Therefore, the present study tested SYBR safe, a non-genotoxic DNA stain, in A. fumigatus gene disruption protocol. The chosen gene was cipC, which has already been disrupted successfully in our laboratory. A deletion cassette was constructed in Saccharomyces cerevisiae and used in A. fumigatus transformation. There was no statistical difference between the tested DNA stains. The success rate of S. cerevisiae transformation was 63.3% for ethidium bromide and 70% for SYBR safe. For A. fumigatus gene disruption, the success rate for ethidium bromide was 100 and 97% for SYBR safe. In conclusion, SYBR safe efficiently replaced ethidium bromide, making this dye a safe and efficient alternative for DNA staining in A. fumigatus gene disruption.
侵袭性曲霉病是一种致死率很高的疾病,主要由烟曲霉引起。现有的药物有限,且这种疾病仍以不可接受的频率发生。基因敲除对于寻找新的药物靶点至关重要。已描述了一种用于烟曲霉基因敲除的有效方案,但该方案需要使用具有遗传毒性的溴化乙锭进行DNA染色。因此,本研究在烟曲霉基因敲除方案中测试了非遗传毒性的DNA染料SYBR safe。所选基因是cipC,该基因在我们实验室已成功敲除。在酿酒酵母中构建缺失盒,并用于烟曲霉转化。测试的DNA染料之间没有统计学差异。溴化乙锭用于酿酒酵母转化的成功率为63.3%,SYBR safe为70%。对于烟曲霉基因敲除,溴化乙锭的成功率为100%,SYBR safe为97%。总之,SYBR safe有效地替代了溴化乙锭,使其成为烟曲霉基因敲除中DNA染色的安全有效替代品。