Summary information and primary citation
- PDB-id
-
8gu6;
DSSR-derived features in text and
JSON formats; DNAproDB
- Class
- RNA binding protein
- Method
- cryo-EM (3.1 Å)
- Summary
- Structure of the sbcas7-11-crrna-ntr-csx29 complex
- Reference
-
Wang X, Yu G, Wen Y, An Q, Li X, Liao F, Lian C, Zhang K,
Yin H, Wei Y, Deng Z, Zhang H (2022): "Target
RNA-guided protease activity in type III-E CRISPR-Cas
system." Nucleic Acids Res.,
50, 12913-12923. doi: 10.1093/nar/gkac1151.
- Abstract
- The type III-E CRISPR-Cas systems are newly identified
adaptive immune systems in prokaryotes that use a single
Cas7-11 protein to specifically cleave target RNA. Cas7-11
could associate with Csx29, a putative caspase-like protein
encoded by the gene frequently found in the type III-E
loci, suggesting a functional linkage between the RNase and
protease activities in type III-E systems. Here, we
demonstrated that target RNA recognition would stimulate
the proteolytic activity of Csx29, and protein Csx30 is the
endogenous substrate. More interestingly, while the cognate
target RNA recognition would activate Csx29, non-cognate
target RNA with the complementary 3' anti-tag sequence
inhibits the enzymatic activity. Csx30 could bind to the
sigma factor RpoE, which may initiate the stress response
after proteolytic cleavage. Combined with biochemical and
structural studies, we have elucidated the mechanisms
underlying the target RNA-guided proteolytic activity of
Csx29. Our work will guide further developments leveraging
this simple RNA targeting system for RNA and
protein-related applications.