Margolis Shally R, Meeske Alexander J
Department of Microbiology, University of Washington, Seattle, WA 98109, USA.
Department of Microbiology, University of Washington, Seattle, WA 98109, USA.
Cell Host Microbe. 2025 Aug 13. doi: 10.1016/j.chom.2025.05.020.
CRISPR-Cas systems confer adaptive immunity to their prokaryotic hosts through the process of adaptation, where sequences are captured from foreign nucleic acids and integrated as spacers in the CRISPR array, thereby enabling crRNA-guided interference against new threats. While the Cas1-2 integrase is critical for adaptation, it is absent from many CRISPR-Cas loci, rendering the mechanism of spacer acquisition unclear for these systems. In this study, we show that the RNA-targeting type VI-A CRISPR system of Listeria seeligeri acquires spacers from DNA substrates through the action of a promiscuous Cas1-2 integrase encoded by a co-occurring type II-C system, in a transcription-independent manner. We further demonstrate that the type II-C integration complex is strongly stimulated by preexisting spacers in a third CRISPR system (type I-B), which imperfectly match phage targets and prime type VI-A adaptation. Altogether, our results reveal an unprecedented degree of communication among CRISPR-Cas loci encoded by a single organism.
CRISPR-Cas系统通过适应过程赋予其原核宿主适应性免疫,在此过程中,序列从外源核酸中捕获并作为间隔序列整合到CRISPR阵列中,从而实现crRNA引导的针对新威胁的干扰。虽然Cas1-2整合酶对适应至关重要,但许多CRISPR-Cas位点中都没有它,这使得这些系统的间隔序列获取机制尚不清楚。在本研究中,我们表明,利氏李斯特菌的RNA靶向VI-A型CRISPR系统通过由同时存在的II-C型系统编码的一种混杂的Cas1-2整合酶的作用,以转录非依赖的方式从DNA底物获取间隔序列。我们进一步证明,II-C型整合复合物在第三个CRISPR系统(I-B型)中被预先存在的间隔序列强烈刺激,这些间隔序列与噬菌体靶标不完全匹配并启动VI-A型适应。总之,我们的结果揭示了单个生物体编码的CRISPR-Cas位点之间前所未有的交流程度。