Development of Ultra-High-Density Screening Tools for Microbial "Omics"

被引:23
作者
Bean, Gordon J. [1 ]
Jaeger, Philipp A. [2 ,3 ]
Bahr, Sondra [4 ]
Ideker, Trey [2 ,3 ,5 ]
机构
[1] Univ Calif San Diego, Bioinformat & Syst Biol Program, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[4] Univ Toronto, Banting & Best Dept Med Res, Terrence Donnelly Ctr Cellular & Biomol Res, Toronto, ON, Canada
[5] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
来源
PLOS ONE | 2014年 / 9卷 / 01期
基金
美国国家卫生研究院;
关键词
SACCHAROMYCES-CEREVISIAE; YEAST; SCALE; MAP;
D O I
10.1371/journal.pone.0085177
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
High-throughput genetic screens in model microbial organisms are a primary means of interrogating biological systems. In numerous cases, such screens have identified the genes that underlie a particular phenotype or a set of gene-gene, gene-environment or protein-protein interactions, which are then used to construct highly informative network maps for biological research. However, the potential test space of genes, proteins, or interactions is typically much larger than current screening systems can address. To push the limits of screening technology, we developed an ultra-high-density, 6144-colony arraying system and analysis toolbox. Using budding yeast as a benchmark, we find that these tools boost genetic screening throughput 4-fold and yield significant cost and time reductions at quality levels equal to or better than current methods. Thus, the new ultra-high-density screening tools enable researchers to significantly increase the size and scope of their genetic screens.
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