Molecular basis of stepwise cyclic tetra-adenylate cleavage by the type III CRISPR ring nuclease Crn1/Sso2081
العنوان: | Molecular basis of stepwise cyclic tetra-adenylate cleavage by the type III CRISPR ring nuclease Crn1/Sso2081 |
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المؤلفون: | Liyang Du, Danping Zhang, Zhipu Luo, Zhonghui Lin |
المصدر: | Nucleic Acids Research. 51:2485-2495 |
بيانات النشر: | Oxford University Press (OUP), 2023. |
سنة النشر: | 2023 |
مصطلحات موضوعية: | Genetics |
الوصف: | The cyclic oligoadenylates (cOAs) act as second messengers of the type III CRISPR immunity system through activating the auxiliary nucleases for indiscriminate RNA degradation. The cOA-degrading nucleases (ring nucleases) provide an ‘off-switch’ regulation of the signaling, thereby preventing cell dormancy or cell death. Here, we describe the crystal structures of the founding member of CRISPR-associated ring nuclease 1 (Crn1) Sso2081 from Saccharolobus solfataricus, alone, bound to phosphate ions or cA4 in both pre-cleavage and cleavage intermediate states. These structures together with biochemical characterizations establish the molecular basis of cA4 recognition and catalysis by Sso2081. The conformational changes in the C-terminal helical insert upon the binding of phosphate ions or cA4 reveal a gate-locking mechanism for ligand binding. The critical residues and motifs identified in this study provide a new insight to distinguish between cOA-degrading and -nondegrading CARF domain-containing proteins. |
تدمد: | 1362-4962 0305-1048 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::8dfbffe171ecb24bd59b3e4e4a530643 https://doi.org/10.1093/nar/gkad101 |
حقوق: | OPEN |
رقم الأكسشن: | edsair.doi...........8dfbffe171ecb24bd59b3e4e4a530643 |
قاعدة البيانات: | OpenAIRE |
تدمد: | 13624962 03051048 |
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