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The Essential Genome of a Bacterium

Overview
Journal Mol Syst Biol
Specialty Molecular Biology
Date 2011 Sep 1
PMID 21878915
Citations 186
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Abstract

Caulobacter crescentus is a model organism for the integrated circuitry that runs a bacterial cell cycle. Full discovery of its essential genome, including non-coding, regulatory and coding elements, is a prerequisite for understanding the complete regulatory network of a bacterial cell. Using hyper-saturated transposon mutagenesis coupled with high-throughput sequencing, we determined the essential Caulobacter genome at 8 bp resolution, including 1012 essential genome features: 480 ORFs, 402 regulatory sequences and 130 non-coding elements, including 90 intergenic segments of unknown function. The essential transcriptional circuitry for growth on rich media includes 10 transcription factors, 2 RNA polymerase sigma factors and 1 anti-sigma factor. We identified all essential promoter elements for the cell cycle-regulated genes. The essential elements are preferentially positioned near the origin and terminus of the chromosome. The high-resolution strategy used here is applicable to high-throughput, full genome essentiality studies and large-scale genetic perturbation experiments in a broad class of bacterial species.

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References
1.
McAdams H, Shapiro L . A bacterial cell-cycle regulatory network operating in time and space. Science. 2003; 301(5641):1874-7. DOI: 10.1126/science.1087694. View

2.
Collier J, Murray S, Shapiro L . DnaA couples DNA replication and the expression of two cell cycle master regulators. EMBO J. 2006; 25(2):346-56. PMC: 1383511. DOI: 10.1038/sj.emboj.7600927. View

3.
Glass J, Assad-Garcia N, Alperovich N, Yooseph S, Lewis M, Maruf M . Essential genes of a minimal bacterium. Proc Natl Acad Sci U S A. 2006; 103(2):425-30. PMC: 1324956. DOI: 10.1073/pnas.0510013103. View

4.
Baba T, Ara T, Hasegawa M, Takai Y, Okumura Y, Baba M . Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection. Mol Syst Biol. 2006; 2:2006.0008. PMC: 1681482. DOI: 10.1038/msb4100050. View

5.
Holtzendorff J, Hung D, Brende P, Reisenauer A, Viollier P, McAdams H . Oscillating global regulators control the genetic circuit driving a bacterial cell cycle. Science. 2004; 304(5673):983-7. DOI: 10.1126/science.1095191. View