Format

Send to

Choose Destination
Science. 2017 Sep 15;357(6356):1113-1118. doi: 10.1126/science.aao0679. Epub 2017 Jul 20.

Structures of the CRISPR genome integration complex.

Wright AV1, Liu JJ1,2, Knott GJ1, Doxzen KW3, Nogales E1,2,4, Doudna JA5,2,3,4,6,7,8.

Author information

1
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
2
Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
3
Biophysics Graduate Group, University of California, Berkeley, Berkeley, CA 94720, USA.
4
Howard Hughes Medical Institute, University of California, Berkeley, Berkeley, CA 94720, USA.
5
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA. doudna@berkeley.edu.
6
Department of Chemistry, University of California, Berkeley, Berkeley, CA 94720, USA.
7
Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA 94720, USA.
8
Center for RNA Systems Biology, University of California, Berkeley, Berkeley, CA 94720, USA.

Abstract

CRISPR-Cas systems depend on the Cas1-Cas2 integrase to capture and integrate short foreign DNA fragments into the CRISPR locus, enabling adaptation to new viruses. We present crystal structures of Cas1-Cas2 bound to both donor and target DNA in intermediate and product integration complexes, as well as a cryo-electron microscopy structure of the full CRISPR locus integration complex, including the accessory protein IHF (integration host factor). The structures show unexpectedly that indirect sequence recognition dictates integration site selection by favoring deformation of the repeat and the flanking sequences. IHF binding bends the DNA sharply, bringing an upstream recognition motif into contact with Cas1 to increase both the specificity and efficiency of integration. These results explain how the Cas1-Cas2 CRISPR integrase recognizes a sequence-dependent DNA structure to ensure site-selective CRISPR array expansion during the initial step of bacterial adaptive immunity.

Comment in

PMID:
28729350
PMCID:
PMC5748385
DOI:
10.1126/science.aao0679
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center