Salama Nina R, Manoil Colin
Division of Human Biology, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N, PO Box 19024, Seattle, WA 98109-1024, USA.
Curr Opin Microbiol. 2006 Jun;9(3):307-11. doi: 10.1016/j.mib.2006.03.002. Epub 2006 Apr 17.
The identification of most or all of the genetic functions that are required for a particular biological process could be achieved through phenotypic studies of high genome-coverage mutant collections. Technologies for creating such collections, in the form of mixed populations or individually arrayed sequence-defined mutants, are now available for numerous bacterial species. The analysis of mixed mutant collections using microarray-based detection procedures appears to be particularly effective in identifying functions required for complex processes such as virulence. The phenotypic analysis of sequence-defined mutant libraries provides a virtually complete identification of nonessential genes required for processes for which suitable screens can be devised. Such libraries also serve as a source of individual mutants for examining the biological relevance of gene associations revealed by transcriptional profiling or homology.
通过对高基因组覆盖度突变体文库进行表型研究,有可能确定特定生物学过程所需的大多数或所有基因功能。现在已有技术可用于创建以混合群体或单独排列的序列定义突变体形式存在的此类文库,适用于众多细菌物种。使用基于微阵列的检测程序分析混合突变体文库,在识别诸如毒力等复杂过程所需的功能方面似乎特别有效。对序列定义突变体文库进行表型分析,几乎可以完全鉴定出可设计合适筛选方法的过程所需的非必需基因。此类文库还可作为单个突变体的来源,用于检验转录谱分析或同源性揭示的基因关联的生物学相关性。