4.5 Article

Structural basis for CRISPR RNA-guided DNA recognition by Cascade

Journal

NATURE STRUCTURAL & MOLECULAR BIOLOGY
Volume 18, Issue 5, Pages 529-U141

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.2019

Keywords

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Funding

  1. The Netherlands Organisation for Scientific Research (NWO) [865.05.001, 863.08.014, 700.58.402]
  2. NWO TOP
  3. UK Engineering and Physical Sciences Research Council and Biotechnology and Biological Sciences Research Council
  4. Wenner-Gren Foundation
  5. Research Councils UK
  6. Life Sciences Research Foundation of HHMI
  7. Deutsche Forschungsgemeinschaft [PU 435/1-1]
  8. The Netherlands Proteomics Center
  9. EPSRC [EP/D033713/1, EP/E036252/1] Funding Source: UKRI
  10. Engineering and Physical Sciences Research Council [EP/E036252/1, EP/D033713/1] Funding Source: researchfish

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The CRISPR (clustered regularly interspaced short palindromic repeats) immune system in prokaryotes uses small guide RNAs to neutralize invading viruses and plasmids. In Escherichia coli, immunity depends on a ribonucleoprotein complex called Cascade. Here we present the composition and low-resolution structure of Cascade and show how it recognizes double-stranded DNA (dsDNA) targets in a sequence-specific manner. Cascade is a 405-kDa complex comprising five functionally essential CRISPR-associated (Cas) proteins (CasA(1)B(2)C(6)D(1)E(1)) and a 61-nucleotide CRISPR RNA (crRNA) with 5'-hydroxyl and 2', 3'-cyclic phosphate termini. The crRNA guides Cascade to dsDNA target sequences by forming base pairs with the complementary DNA strand while displacing the noncomplementary strand to form an R-loop. Cascade recognizes target DNA without consuming ATP, which suggests that continuous invader DNA surveillance takes place without energy investment. The structure of Cascade shows an unusual seahorse shape that undergoes conformational changes when it binds target DNA.

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