Envelope stress is a trigger of CRISPR RNA‐mediated DNA silencing in Escherichia coli

A widespread feature in the genomes of most bacteria and archaea is an array of clustered, regularly interspaced short palindromic repeats (CRISPRs) that, together with a group of CRISPR‐associated (Cas) proteins, mediate immunity against invasive nucleic acids such as plasmids and viruses. Here, the CRISPR‐Cas system was activated in cells expressing a plasmid‐encoded protein that was targeted to the twin‐arginine translocation (Tat) pathway. Expression of this Tat substrate resulted in upregulation of the Cas enzymes and subsequent silencing of the encoding plasmid in a manner that required the BaeSR two‐component regulatory system, which is known to respond to extracytoplasmic stress. Furthermore, we confirm that the CasCDE enzymes form a stable ternary complex and appear to function as the catalytic core of the Cas system to process CRISPR RNA into its mature form. Taken together, our results indicate that the CRISPR‐Cas system targets DNA directly as part of a defence mechanism in bacteria that is overlapping with but not limited to phage infection.

[1]  Jennifer A. Doudna,et al.  Sequence- and Structure-Specific RNA Processing by a CRISPR Endonuclease , 2010, Science.

[2]  Stan J. J. Brouns,et al.  H‐NS‐mediated repression of CRISPR‐based immunity in Escherichia coli K12 can be relieved by the transcription activator LeuO , 2010, Molecular microbiology.

[3]  J. García-Martínez,et al.  Diversity of CRISPR loci in Escherichia coli. , 2010, Microbiology.

[4]  Rolf Wagner,et al.  Identification and characterization of E. coli CRISPR‐cas promoters and their silencing by H‐NS , 2010, Molecular microbiology.

[5]  L. Marraffini,et al.  Self vs. non-self discrimination during CRISPR RNA-directed immunity , 2009, Nature.

[6]  B. Graveley,et al.  RNA-Guided RNA Cleavage by a CRISPR RNA-Cas Protein Complex , 2009, Cell.

[7]  Shiraz A. Shah,et al.  CRISPR families of the crenarchaeal genus Sulfolobus: bidirectional transcription and dynamic properties , 2009, Molecular microbiology.

[8]  G. Storz,et al.  Regulatory RNAs in Bacteria , 2009, Cell.

[9]  L. Marraffini,et al.  CRISPR Interference Limits Horizontal Gene Transfer in Staphylococci by Targeting DNA , 2008, Science.

[10]  R. Terns,et al.  Cas6 is an endoribonuclease that generates guide RNAs for invader defense in prokaryotes. , 2008, Genes & development.

[11]  R. Terns,et al.  Prokaryotic silencing (psi)RNAs in Pyrococcus furiosus. , 2008, RNA.

[12]  Stan J. J. Brouns,et al.  Small CRISPR RNAs Guide Antiviral Defense in Prokaryotes , 2008, Science.

[13]  D. Putnam,et al.  Engineered bacterial outer membrane vesicles with enhanced functionality. , 2008, Journal of molecular biology.

[14]  Charles DeLisi,et al.  Classifying transcription factor targets and discovering relevant biological features , 2008, Biology Direct.

[15]  Ibtissem Grissa,et al.  CRISPRcompar: a website to compare clustered regularly interspaced short palindromic repeats , 2008, Nucleic Acids Res..

[16]  V. Kunin,et al.  CRISPR — a widespread system that provides acquired resistance against phages in bacteria and archaea , 2008, Nature Reviews Microbiology.

[17]  A. Ishihama,et al.  Involvement of multiple transcription factors for metal-induced spy gene expression in Escherichia coli. , 2008, Journal of biotechnology.

[18]  Philippe Horvath,et al.  Phage Response to CRISPR-Encoded Resistance in Streptococcus thermophilus , 2007, Journal of bacteriology.

[19]  Ibtissem Grissa,et al.  CRISPRFinder: a web tool to identify clustered regularly interspaced short palindromic repeats , 2007, Nucleic Acids Res..

[20]  V. Kunin,et al.  Evolutionary conservation of sequence and secondary structures in CRISPR repeats , 2007, Genome Biology.

[21]  Adam C. Fisher,et al.  An essential role for the DnaK molecular chaperone in stabilizing over-expressed substrate proteins of the bacterial twin-arginine translocation pathway. , 2007, Journal of molecular biology.

[22]  R. Barrangou,et al.  CRISPR Provides Acquired Resistance Against Viruses in Prokaryotes , 2007, Science.

[23]  R. Garrett,et al.  A putative viral defence mechanism in archaeal cells. , 2006, Archaea.

[24]  M. Shuler,et al.  A three-channel microfluidic device for generating static linear gradients and its application to the quantitative analysis of bacterial chemotaxis. , 2006, Lab on a chip.

[25]  H. Mori,et al.  Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection , 2006, Molecular systems biology.

[26]  S. Frielingsdorf,et al.  Unassisted membrane insertion as the initial step in DeltapH/Tat-dependent protein transport. , 2006, Journal of molecular biology.

[27]  T. Brüser,et al.  Targeting of Unfolded PhoA to the TAT Translocon of Escherichia coli* , 2005, Journal of Biological Chemistry.

[28]  M. DeLisa,et al.  Twin-Arginine Translocation of Active Human Tissue Plasminogen Activator in Escherichia coli , 2005, Applied and Environmental Microbiology.

[29]  Daniel H. Haft,et al.  A Guild of 45 CRISPR-Associated (Cas) Protein Families and Multiple CRISPR/Cas Subtypes Exist in Prokaryotic Genomes , 2005, PLoS Comput. Biol..

[30]  A. Yamaguchi,et al.  Indole induces the expression of multidrug exporter genes in Escherichia coli , 2004, Molecular microbiology.

[31]  A. Goffeau,et al.  Complete sequence and comparative genome analysis of the dairy bacterium Streptococcus thermophilus , 2004, Nature Biotechnology.

[32]  J. M. Thomson,et al.  Argonaute2 Is the Catalytic Engine of Mammalian RNAi , 2004, Science.

[33]  G. Georgiou,et al.  Phage Shock Protein PspA of Escherichia coli Relieves Saturation of Protein Export via the Tat Pathway , 2004, Journal of bacteriology.

[34]  George Georgiou,et al.  Folding quality control in the export of proteins by the bacterial twin-arginine translocation pathway , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[35]  T. Raivio,et al.  A third envelope stress signal transduction pathway in Escherichia coli , 2002, Molecular microbiology.

[36]  George Georgiou,et al.  Genetic Analysis of the Twin Arginine Translocator Secretion Pathway in Bacteria* , 2002, The Journal of Biological Chemistry.

[37]  H. Nikaido,et al.  The BaeSR Two-Component Regulatory System Activates Transcription of the yegMNOB (mdtABCD) Transporter Gene Cluster in Escherichia coli and Increases Its Resistance to Novobiocin and Deoxycholate , 2002, Journal of bacteriology.

[38]  A. Hüttenhofer,et al.  Identification of 86 candidates for small non-messenger RNAs from the archaeon Archaeoglobus fulgidus , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[39]  H. Lill,et al.  Transport of cytochrome c derivatives by the bacterial Tat protein translocation system , 2001, Molecular microbiology.

[40]  I. Oresnik,et al.  Identification of a twin‐arginine leader‐binding protein , 2001, Molecular microbiology.

[41]  B. Wanner,et al.  One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[42]  O. Fayet,et al.  A set of pBR322-compatible plasmids allowing the testing of chaperone-assisted folding of proteins overexpressed in Escherichia coli. , 1997, Analytical biochemistry.

[43]  J. Dworkin,et al.  The Escherichia coli phage‐shock‐protein (psp) operon , 1997, Molecular microbiology.

[44]  D. Court,et al.  Genetic analysis of the rnc operon of Escherichia coli , 1989, Journal of bacteriology.

[45]  T. Raivio,et al.  Two-component signaling and gram negative envelope stress response systems. , 2008, Advances in experimental medicine and biology.