Abstract
Type III CRISPR-Cas executes a multifaceted anti-phage response, activating effectors such as a nuclease or membrane depolarizer. In a recent Cell paper, Baca and Majumder et al.1 report an accessory effector, Cad1, which deaminates ATP into ITP, causing ITP accumulation and host growth arrest, thereby inhibiting phage propagation.
Originalsprog | Engelsk |
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Tidsskrift | Cell Host and Microbe |
Vol/bind | 33 |
Udgave nummer | 1 |
Sider (fra-til) | 8-10 |
Antal sider | 3 |
ISSN | 1931-3128 |
DOI |
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Status | Udgivet - 2025 |
Bibliografisk note
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