In Vivo Protein Interactions and Complex Formation in the Pectobacterium atrosepticum Subtype I-F CRISPR/Cas System
@article{Richter2012InVP, title={In Vivo Protein Interactions and Complex Formation in the Pectobacterium atrosepticum Subtype I-F CRISPR/Cas System}, author={Corinna Richter and Tamzin Gristwood and James S. Clulow and Peter C. Fineran}, journal={PLoS ONE}, year={2012}, volume={7} }
Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) and their associated proteins (Cas; CRISPR associated) are a bacterial defense mechanism against extra-chromosomal elements. CRISPR/Cas systems are distinct from other known defense mechanisms insofar as they provide acquired and heritable immunity. Resistance is accomplished in multiple stages in which the Cas proteins provide the enzymatic machinery. Importantly, subtype-specific proteins have been shown to form complexes in…
76 Citations
Interference activity of a minimal Type I CRISPR–Cas system from Shewanella putrefaciens
- BiologyNucleic acids research
- 2015
Interference assays based on plasmid conjugation demonstrated that this CRISPR-Cas system is active in vivo and that activity is dependent on the recognition of the dinucleotide GG PAM (Protospacer Adjacent Motif) sequence and crRNA abundance.
CRISPR RNA and anti-CRISPR protein binding to the Xanthomonas albilineans Csy1-Csy2 heterodimer in the type I-F CRISPR-Cas system
- BiologyThe Journal of Biological Chemistry
- 2018
The results provide information about the order of events during the formation of the multisubunit crRNA-guided surveillance complex and suggest that the Acr protein inactivating type I-F CRISPR-Cas systems has broad specificity.
Cas1 and the Csy complex are opposing regulators of Cas2/3 nuclease activity
- BiologyProceedings of the National Academy of Sciences
- 2017
It is shown that the Cas2/3 fusion protein from Pseudomonas aeruginosa stably associates with the Cas1 adaptation protein, forming a 375-kDa propeller-shaped Cas1–2/ 3 complex, and how Cas1 and the target-bound Csy complex play opposing roles in the regulation of Cas 2/3 nuclease activity is explained.
The subtype I-F CRISPR-Cas system influences pathogenicity island retention in Pectobacterium atrosepticum via crRNA generation and Csy complex formation.
- BiologyBiochemical Society transactions
- 2013
How chromosomal targeting by CRISPR-Cas can cause large-scale genome deletions, which can ultimately influence bacterial evolution and pathogenicity is addressed.
Mechanisms of Type I-E and I-F CRISPR-Cas Systems in Enterobacteriaceae.
- BiologyEcoSal Plus
- 2019
The study of several members of the Gram-negative Enterobacteriaceae family, especially Escherichia coli and Pectobacterium atrosepticum, have provided significant insights into the mechanisms of CRISPR-Cas immunity.
Cytotoxic Chromosomal Targeting by CRISPR/Cas Systems Can Reshape Bacterial Genomes and Expel or Remodel Pathogenicity Islands
- BiologyPLoS genetics
- 2013
In DNA–targeting CRISPR/Cas systems, chromosomal interference is deleterious by causing DNA damage and providing a strong selective pressure for genome alterations, which may have consequences for bacterial evolution and pathogenicity.
Spacer capture and integration by a type I-F Cas1–Cas2-3 CRISPR adaptation complex
- BiologyProceedings of the National Academy of Sciences
- 2017
A sensitive in vitro assay was developed and demonstrated that Cas1–Cas2-3 catalyzed spacer integration into CRISPR arrays independent of Cas3 activity, and insight is provided into the structure of protospacer-bound type I Cas 1–Cas 2-3 adaptation complexes and their integration mechanism.
DNA and RNA interference mechanisms by CRISPR-Cas surveillance complexes
- BiologyFEMS microbiology reviews
- 2015
The knowledge on the molecular mechanism involved in the DNA and RNA interference stages of type I (Cascade: CRISPR-associated complex for antiviral defense), type II (Cas9) and type III (Csm, Cmr) CRISpr-Cas systems are reviewed.
Reconstitution of CRISPR adaptation in vitro and its detection by PCR.
- BiologyMethods in enzymology
- 2019
Functions and Applications of RNA‐Guided CRISPR‐Cas Immune Systems
- Biology
- 2014
The inheritable and hypervariable nature of these loci can be used to track the phylogenetic path of an organism and reveal the evolutionary interplay between hosts and their viruses.
References
SHOWING 1-10 OF 57 REFERENCES
Csy4 is responsible for CRISPR RNA processing in Pectobacterium atrosepticum
- BiologyRNA biology
- 2011
This study provides the first in vivo evidence that the CRISPR endoribonuclease Csy4 generates crRNAs in its native host and characterizes the operonic transcription of the cas cluster.
Characterization of the CRISPR/Cas Subtype I-A System of the Hyperthermophilic Crenarchaeon Thermoproteus tenax
- BiologyJournal of bacteriology
- 2012
Seven CRISPR loci in the genome of the crenarchaeon Thermoproteus tenax that include spacers with significant similarity not only to archaeal viruses but also to T. tenax genes are investigated to provide insights into the specialized mechanisms of an archaealing CRISpr/Cas system and allow selective functional analyses of Cas protein complexes in the future.
Cas5d protein processes pre-crRNA and assembles into a cascade-like interference complex in subtype I-C/Dvulg CRISPR-Cas system.
- BiologyStructure
- 2012
Structural and Functional Characterization of an Archaeal Clustered Regularly Interspaced Short Palindromic Repeat (CRISPR)-associated Complex for Antiviral Defense (CASCADE)*
- BiologyThe Journal of Biological Chemistry
- 2011
The structural and functional characterization of an archaeal CASCADE (aCASCADE) from Sulfolobus solfataricus is reported and a general subunit architecture for CASCade in other bacteria and Archaea is proposed.
Unification of Cas protein families and a simple scenario for the origin and evolution of CRISPR-Cas systems
- BiologyBiology Direct
- 2011
Evidence is presented that large subunits contained in most of the CRISPR-Cas systems could be homologous to Cas10 proteins which contain a polymerase-like Palm domain and are predicted to be enzymatically active in Type III CRISpr-cas systems but inactivated in Type I systems.
RNA-guided complex from a bacterial immune system enhances target recognition through seed sequence interactions
- BiologyProceedings of the National Academy of Sciences
- 2011
It is shown that the Csy proteins (Csy1–4) assemble into a 350 kDa ribonucleoprotein complex that facilitates target recognition by enhancing sequence-specific hybridization between the CRISPR RNA and complementary target sequences.
Non-Identity-Mediated CRISPR-Bacteriophage Interaction Mediated via the Csy and Cas3 Proteins
- BiologyJournal of bacteriology
- 2011
It is determined that only spacer 1, which is not identical to any region of the DMS3 genome, mediates the CRISPR-dependent loss of biofilm formation, and evidence suggests that gene 42 of phage D MS3 (DMS3-42) is targeted byCRISPR2 spacer1 and that this targeting tolerates multiple point mutations between the spacer and DMS 3-42 target sequence.
Structure of a CRISPR-associated protein Cas2 from Desulfovibrio vulgaris.
- Chemistry, BiologyActa crystallographica. Section F, Structural biology and crystallization communications
- 2010
A 1.35 Å resolution crystal structure of Cas2 from the bacterium Desulfovibrio vulgaris (DvuCas2) is reported, and the Dvu Cas2 dimer is stabilized by a distinctive network of hydrophilic cross-protomer side-chain interactions.
Structure and mechanism of the CMR complex for CRISPR-mediated antiviral immunity.
- Biology, ChemistryMolecular cell
- 2012