探索天然产物作用方式的化学遗传学方法。

Andres Lopez, Ainslie B Parsons, Corey Nislow, Guri Giaever, Charles Boone
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引用次数: 31

摘要

确定生物活性化合物(包括天然产物)的作用方式是化学生物学中的一个核心问题。由于许多基因从酵母到人类是保守的,并且许多强大的基因组学工具和方法已经开发出来,酵母在化学遗传学领域做出了重大贡献。这组条形码酵母缺失突变体,包括大约5000个存活的单倍体和纯合二倍体缺失突变体,以及大约6000个杂合缺失突变体,包含大约1000个必需基因,被证明对识别化学-遗传相互作用和破译复合作用模式具有很高的信息。使细胞对特定药物过敏的基因缺失确定了缓冲细胞对抗药物毒性作用的途径,从而为基因和化合物功能提供了线索。此外,具有相似化学-遗传特征的化合物通常会干扰相似的靶通路。基因剂量可以用来发现化合物和它们的目标之间的联系。例如,一种抗真菌化合物的单倍不全谱分析,其中大约6000个杂合二倍体缺失突变体被标记为对化合物过敏,可以直接识别目标。在其他真菌物种中创建缺失突变集合,包括主要的人类真菌病原体白色念珠菌,将扩展我们的化学基因组学工具集,使我们能够直接筛选抗真菌先导药物。酵母缺失突变体的收集也被用于绘制从全基因组合成致死筛选中获得的大规模遗传相互作用数据,并将这些数据与化学遗传数据相结合,应该为将化合物与其目标途径联系起来提供一个强大的系统。化学遗传学在酵母中的广泛应用,有可能为所有大约6000个酵母基因中的大多数开发出小分子抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemical-genetic approaches for exploring the mode of action of natural products.

Determining the mode of action of bioactive compounds, including natural products, is a central problem in chemical biology. Because many genes are conserved from the yeast Saccharomyces cerevisiae to humans and a number of powerful genomics tools and methodologies have been developed for this model system, yeast is making a major contribution to the field of chemical genetics. The set of barcoded yeast deletion mutants, including the set of approximately 5000 viable haploid and homozygous diploid deletion mutants and the complete set of approximately 6000 heterozygous deletion mutants, containing the set of approximately 1000 essential genes, are proving highly informative for identifying chemical-genetic interactions and deciphering compound mode of action. Gene deletions that render cells hypersensitive to a specific drug identify pathways that buffer the cell against the toxic effects of the drug and thereby provide clues about both gene and compound function. Moreover, compounds that show similar chemical-genetic profiles often perturb similar target pathways. Gene dosage can be exploited to discover connections between compounds and their targets. For example, haploinsufficiency profiling of an antifungal compound, in which the set of approximately 6000 heterozygous diploid deletion mutants are scored for hypersensitivity to a compound, may identify the target directly. Creating deletion mutant collections in other fungal species, including the major human fungal pathogen Candida albicans, will expand our chemical genomics tool set, allowing us to screen for antifungal lead drugs directly. The yeast deletion mutant collection is also being exploited to map large-scale genetic interaction data obtained from genome-wide synthetic lethal screens and the integration of this data with chemical genetic data should provide a powerful system for linking compounds to their target pathway. Extensive application of chemical genetics in yeast has the potential to develop a small molecule inhibitor for the majority of all approximately 6000 yeast genes.

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