Quantitative approaches to study phenotypic effects of large-scale genetic perturbations

被引:1
作者
Mueller, Janina [1 ]
Bollenbach, Tobias [1 ,2 ]
机构
[1] Univ Cologne, Inst Biol Phys, D-50931 Cologne, Germany
[2] Univ Cologne, Ctr Data & Simulat Sci, D-50931 Cologne, Germany
关键词
HIGH-THROUGHPUT; CHEMICAL GENOMICS; ESCHERICHIA-COLI; CRISPR; CONSTRUCTION; PLATFORM; REVEALS;
D O I
10.1016/j.mib.2023.102333
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
How microbes interact with their environment and how the complex interplay of their genes enables them to survive and thrive under stress is a fundamental question in microbial system biology, which is also important from a public health perspective. Large-scale studies of gene-gene, gene-drug, and drug-drug interactions have proven to be powerful tools for elucidating gene function and functional modules in the cell. Approaches that systematically quantify phenotypes in libraries of microbial strains with genome-wide genetic perturbations are crucial for progress in this area. Here, we review recent advances in this field, and point out applications to the study of gene-drug interactions. We highlight newly developed techniques for the rapid generation of genome-wide mutant libraries and the high-throughput measurement of more complex phenotypes and other observables, such as cell morphology or thermal stability of the proteome.
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页数:7
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