A multi-scale expression and regulation knowledge base for Escherichia coli

被引:21
作者
Lamoureux, Cameron R. [1 ]
Decker, Katherine T. [1 ]
Sastry, Anand, V [1 ]
Rychel, Kevin [1 ]
Gao, Ye [1 ]
McConn, John Luke [1 ]
Zielinski, Daniel C. [1 ]
Palsson, Bernhard O. [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Tech Univ Denmark, Novo Nord Fdn Ctr Biosustainabil, Kemitorvet,Bldg 220, DK-2800 Lyngby, Denmark
关键词
UNCHARACTERIZED TRANSCRIPTION FACTORS; INDEPENDENT COMPONENT ANALYSIS; CATABOLITE ACTIVATOR PROTEIN; RNA-SEQ; GENE-REGULATION; REVEALS; FNR; SYSTEM; IRON; CONVERSION;
D O I
10.1093/nar/gkad750
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcriptomic data is accumulating rapidly; thus, scalable methods for extracting knowledge from this data are critical. Here, we assembled a top-down expression and regulation knowledge base for Escherichia coli. The expression component is a 1035-sample, high-quality RNA-seq compendium consisting of data generated in our lab using a single experimental protocol. The compendium contains diverse growth conditions, including: 9 media; 39 supplements, including antibiotics; 42 heterologous proteins; and 76 gene knockouts. Using this resource, we elucidated global expression patterns. We used machine learning to extract 201 modules that account for 86% of known regulatory interactions, creating the regulatory component. With these modules, we identified two novel regulons and quantified systems-level regulatory responses. We also integrated 1675 curated, publicly-available transcriptomes into the resource. We demonstrated workflows for analyzing new data against this knowledge base via deconstruction of regulation during aerobic transition. This resource illuminates the E. coli transcriptome at scale and provides a blueprint for top-down transcriptomic analysis of non-model organisms. Graphical Abstract
引用
收藏
页码:10176 / 10193
页数:18
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