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.
Original language | English |
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Journal | Cell Host and Microbe |
Volume | 33 |
Issue number | 1 |
Pages (from-to) | 8-10 |
Number of pages | 3 |
ISSN | 1931-3128 |
DOIs |
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Publication status | Published - 2025 |
Bibliographical note
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