4.8 Article

A Comprehensive, CRISPR-based Functional Analysis of Essential Genes in Bacteria

Journal

CELL
Volume 165, Issue 6, Pages 1493-1506

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2016.05.003

Keywords

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Funding

  1. UCSF Center for Systems and Synthetic Biology
  2. Stanford Graduate Fellowship
  3. Stanford Agilent Fellowship
  4. Foundation Grant (from Canadian Institutes of Health Research)
  5. Canada Research Chair
  6. NIH [F32 GM108222, DA036858, OD017887, R01 DA036858, DP2-OD006466, NIH R01 GM102790]
  7. HHMI
  8. NSF [MCB-1149328]

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Essential gene functions underpin the core reactions required for cell viability, but their contributions and relationships are poorly studied in vivo. Using CRISPR interference, we created knockdowns of every essential gene in Bacillus subtilis and probed their phenotypes. Our high-confidence essential gene network, established using chemical genomics, showed extensive interconnections among distantly related processes and identified modes of action for uncharacterized antibiotics. Importantly, mild knockdown of essential gene functions significantly reduced stationary-phase survival without affecting maximal growth rate, suggesting that essential protein levels are set to maximize outgrowth from stationary phase. Finally, high-throughput microscopy indicated that cell morphology is relatively insensitive to mild knockdown but profoundly affected by depletion of gene function, revealing intimate connections between cell growth and shape. Our results provide a framework for systematic investigation of essential gene functions in vivo broadly applicable to diverse microorganisms and amenable to comparative analysis.

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