7OXD
Crystal structure of Scytonema hofmanni transposition protein TniQ
Summary for 7OXD
| Entry DOI | 10.2210/pdb7oxd/pdb |
| Descriptor | ShTniQ, ZINC ION (3 entities in total) |
| Functional Keywords | transposition protein, zinc-finger protein, dna binding protein |
| Biological source | Scytonema hofmannii |
| Total number of polymer chains | 1 |
| Total formula weight | 17761.38 |
| Authors | Querques, I.,Jinek, M. (deposition date: 2021-06-22, release date: 2021-12-01, Last modification date: 2024-06-19) |
| Primary citation | Querques, I.,Schmitz, M.,Oberli, S.,Chanez, C.,Jinek, M. Target site selection and remodelling by type V CRISPR-transposon systems. Nature, 599:497-502, 2021 Cited by PubMed Abstract: Canonical CRISPR-Cas systems provide adaptive immunity against mobile genetic elements. However, type I-F, I-B and V-K systems have been adopted by Tn7-like transposons to direct RNA-guided transposon insertion. Type V-K CRISPR-associated transposons rely on the pseudonuclease Cas12k, the transposase TnsB, the AAA+ ATPase TnsC and the zinc-finger protein TniQ, but the molecular mechanism of RNA-directed DNA transposition has remained elusive. Here we report cryo-electron microscopic structures of a Cas12k-guide RNA-target DNA complex and a DNA-bound, polymeric TnsC filament from the CRISPR-associated transposon system of the photosynthetic cyanobacterium Scytonema hofmanni. The Cas12k complex structure reveals an intricate guide RNA architecture and critical interactions mediating RNA-guided target DNA recognition. TnsC helical filament assembly is ATP-dependent and accompanied by structural remodelling of the bound DNA duplex. In vivo transposition assays corroborate key features of the structures, and biochemical experiments show that TniQ restricts TnsC polymerization, while TnsB interacts directly with TnsC filaments to trigger their disassembly upon ATP hydrolysis. Together, these results suggest that RNA-directed target selection by Cas12k primes TnsC polymerization and DNA remodelling, generating a recruitment platform for TnsB to catalyse site-specific transposon insertion. Insights from this work will inform the development of CRISPR-associated transposons as programmable site-specific gene insertion tools. PubMed: 34759315DOI: 10.1038/s41586-021-04030-z PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.3 Å) |
Structure validation
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