Reconstitution of CRISPR adaptation in vitro and its detection by PCR.


Journal

Methods in enzymology
ISSN: 1557-7988
Titre abrégé: Methods Enzymol
Pays: United States
ID NLM: 0212271

Informations de publication

Date de publication:
2019
Historique:
entrez: 30 1 2019
pubmed: 30 1 2019
medline: 15 11 2019
Statut: ppublish

Résumé

CRISPR adaptation is the initial step in CRISPR-Cas immunity and involves the acquisition of foreign invading DNA. Acquisition is facilitated by the almost universally conserved proteins Cas1 and Cas2, which form an adaptation complex. The Cas1-Cas2 complex binds fragments of invading DNA, completes final processing, and catalyzes integration into specific host loci called CRISPR arrays. Structural and biochemical studies from reconstituted complexes have provided mechanistic insight into how CRISPR adaptation occurs; however, these studies have been limited to a narrow subset of CRISPR-Cas types and may not be representative of the other types. Here we describe methods for the purification of the type I-F CRISPR adaptation complex (Cas1:Cas2-3) from Pectobacterium atrosepticum, purification of the DNA architectural protein integration host factor (IHF), and a sensitive PCR-based in vitro integration assay. This assay could easily be used to investigate mechanisms of CRISPR adaptation in other CRISPR-Cas systems, including the roles of accessory proteins.

Identifiants

pubmed: 30691653
pii: S0076-6879(18)30439-7
doi: 10.1016/bs.mie.2018.10.024
pii:
doi:

Substances chimiques

CRISPR-Associated Proteins 0
Integration Host Factors 0
DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

411-433

Informations de copyright

© 2019 Elsevier Inc. All rights reserved.

Auteurs

Robert D Fagerlund (RD)

Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand. Electronic address: robert.fagerlund@otago.ac.nz.

Timothy J Ferguson (TJ)

Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.

Howard W R Maxwell (HWR)

Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.

Helen K Opel-Reading (HK)

Department of Biochemistry, University of Otago, Dunedin, New Zealand.

Kurt L Krause (KL)

Department of Biochemistry, University of Otago, Dunedin, New Zealand.

Peter C Fineran (PC)

Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand. Electronic address: peter.fineran@otago.ac.nz.

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Classifications MeSH