Identification and characterization of E. coli CRISPR‐cas promoters and their silencing by H‐NS

@article{Pul2010IdentificationAC,
  title={Identification and characterization of E. coli CRISPR‐cas promoters and their silencing by H‐NS},
  author={{\"U}mit Pul and Reinhild Wurm and Zihni Arslan and Ren{\'e} Geissen and Nina Hofmann and Rolf Wagner},
  journal={Molecular Microbiology},
  year={2010},
  volume={75}
}
Inheritable bacterial defence systems against phage infection and foreign DNA, termed CRISPR (clustered regularly interspaced short palindromic repeats), consist of cas protein genes and repeat arrays interspaced with sequences originating from invaders. The Cas proteins together with processed small spacer‐repeat transcripts (crRNAs) cause degradation of penetrated foreign DNA by unknown mechanisms. Here, we have characterized previously unidentified promoters of the Escherichia coli CRISPR… 
Envelope stress is a trigger of CRISPR RNA‐mediated DNA silencing in Escherichia coli
TLDR
It is confirmed 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.
Functional Characterization of CRISPR-Cas System in the Ethanologenic Bacterium Zymomonas mobilis ZM4
TLDR
Conclusively, the Type I-F CRISPR-Cas system in Z. mobilis ZM4 is active to functionally defense the invading DNA elements.
H‐NS‐mediated repression of CRISPR‐based immunity in Escherichia coli K12 can be relieved by the transcription activator LeuO
TLDR
It is demonstrated that in E. coli H‐NS and LeuO are antagonistic regulators of CRISPR‐based immunity, which leads to enhanced protection against phage infection.
CRISPR: A Bacterial Immunity System Based on Small RNAs
TLDR
The CRISPR system has been proven to confer adaptive and inheritable immunity against foreign nucleic acid and resembles the RNA interference phenomenon of eukaryotes, an important control and defense tool with widespread applications in research and medical developments.
Correction: CRISPR Content Correlates with the Pathogenic Potential of Escherichia coli
TLDR
Findings support an evolutionary connection between CRISPR and pathogenicity in E. coli.
Modulation of CRISPR locus transcription by the repeat-binding protein Cbp1 in Sulfolobus
TLDR
It is proposed that Cbp1 modulates production of longer pre-crRNA transcripts from CRISPR loci, a possible mechanism is that it minimizes interference from potential transcriptional signals carried on spacers deriving from A-T-rich genetic elements and, occasionally, on DNA repeats.
CRISPR Content Correlates with the Pathogenic Potential of Escherichia coli
TLDR
Findings support an evolutionary connection between CRISPR and pathogenicity in E. coli.
Transcription, processing and function of CRISPR cassettes in Escherichia coli
TLDR
Using an engineered strain with genomically located spacer matching phage λ, it is shown that endogenous levels of CRISPR cassette and cas genes expression allow only weak protection against infection with the phage, however, derepression of the CRISpr/Cas system by disruption of the hns gene leads to high level of protection.
Mechanism and engineering of CRISPR-associated endonucleases
TLDR
It is revealed that Cas9 can be programmed to target single-stranded RNA substrates for both high-affinity binding and site- specific cleavage using PAM-presenting oligonucleotides and that RNA targeting by Cas9 has the potential to transform the study of RNA function, much as site-specific DNA targeting has revolutionized genetic and genomic research.
...
1
2
3
4
5
...

References

SHOWING 1-10 OF 81 REFERENCES
Cas6 is an endoribonuclease that generates guide RNAs for invader defense in prokaryotes.
TLDR
This work has identified Pyrococcus furiosus Cas6 as a novel endoribonuclease that cleaves CRISPR RNAs within the repeat sequences to release individual invader targeting RNAs.
RNA-Guided RNA Cleavage by a CRISPR RNA-Cas Protein Complex
A putative RNA-interference-based immune system in prokaryotes: computational analysis of the predicted enzymatic machinery, functional analogies with eukaryotic RNAi, and hypothetical mechanisms of action
TLDR
It appears most likely that CASS is a prokaryotic system of defense against phages and plasmids that functions via the RNAi mechanism, which seems to involve integration of fragments of foreign genes into archaeal and bacterial chromosomes yielding heritable immunity to the respective agents.
Short motif sequences determine the targets of the prokaryotic CRISPR defence system.
TLDR
It is shown that the conservation of proto-spacer adjacent motifs (PAMs) is a common theme for the most diverse CRISPR systems, implying that there is aCRISPR-type-specific (motif-directed) choice of the spacers, which subsequently determines the interference target.
Prokaryotic silencing (psi)RNAs in Pyrococcus furiosus.
TLDR
These results identify the principal products of the CRISPR loci as small psiRNAs comprised primarily of invader-targeting sequence with perhaps only 5-10 nucleotides ofCRISPR repeat sequence, which are the most abundant CRISpr RNA species in P. furiosus.
Identification of genes that are associated with DNA repeats in prokaryotes
TLDR
A novel family of repetitive DNA sequences that is present among both domains of the prokaryotes but absent from eukaryotes or viruses is studied, characterized by direct repeats, varying in size from 21 to 37 bp, interspaced by similarly sized non‐repetitive sequences.
Silencing of xenogeneic DNA by H-NS-facilitation of lateral gene transfer in bacteria by a defense system that recognizes foreign DNA.
TLDR
This work has shown that H-NS, an abundant nucleoid-associated protein in enteric bacteria and related species, can recognize and selectively silence the expression of foreign DNA with higher adenine and thymine content relative to the resident genome, a property that has made this molecule an almost universal regulator of virulence determinants inEnteric bacteria.
Phage Response to CRISPR-Encoded Resistance in Streptococcus thermophilus
TLDR
It is shown through the analyses of 20 mutant phages that virulent phages are rapidly evolving through single nucleotide mutations as well as deletions, in response to CRISPR1.
Diversity, Activity, and Evolution of CRISPR Loci in Streptococcus thermophilus
TLDR
A novel Streptococcus thermophilus locus is characterized, and its ability to integrate novel spacers in response to bacteriophage is experimentally demonstrated, and it is hypothesized that the level of diversity is correlated with relative CRISPR activity and proposed that the activity is highest for CRISpr1, followed by CRIS PR3, while CRISP2 may be degenerate.
...
1
2
3
4
5
...