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Structure Studies of the CRISPR-Csm Complex Reveal Mechanism of Co-transcriptional Interference
Author(s) -
Lilan You,
Jun Ma,
Jiuyu Wang,
Daria Artamonova,
Min Wang,
Liang Liu,
Hua Xiang,
Konstantin Severinov,
Xinzheng Zhang,
Yanli Wang
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.10.052
Subject(s) - biology , crispr , mechanism (biology) , interference (communication) , rna interference , genetics , computational biology , evolutionary biology , microbiology and biotechnology , gene , rna , philosophy , channel (broadcasting) , epistemology , electrical engineering , engineering
Csm, a type III-A CRISPR-Cas interference complex, is a CRISPR RNA (crRNA)-guided RNase that also possesses target RNA-dependent DNase and cyclic oligoadenylate (cOA) synthetase activities. However, the structural features allowing target RNA-binding-dependent activation of DNA cleavage and cOA generation remain unknown. Here, we report the structure of Csm in complex with crRNA together with structures of cognate or non-cognate target RNA bound Csm complexes. We show that depending on complementarity with the 5' tag of crRNA, the 3' anti-tag region of target RNA binds at two distinct sites of the Csm complex. Importantly, the interaction between the non-complementary anti-tag region of cognate target RNA and Csm1 induces a conformational change at the Csm1 subunit that allosterically activates DNA cleavage and cOA generation. Together, our structural studies provide crucial insights into the mechanistic processes required for crRNA-meditated sequence-specific RNA cleavage, RNA target-dependent non-specific DNA cleavage, and cOA generation.

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