School of Biology, University of St Andrews, St Andrews, Fife KY16 9ST, U.K.
Biochem J. 2024 Jun 19;481(12):793-804. doi: 10.1042/BCJ20240151.
CRISPR-Cas systems confer adaptive immunity in prokaryotes, facilitating the recognition and destruction of invasive nucleic acids. Type III CRISPR systems comprise large, multisubunit ribonucleoprotein complexes with a catalytic Cas10 subunit. When activated by the detection of foreign RNA, Cas10 generates nucleotide signalling molecules that elicit an immune response by activating ancillary effector proteins. Among these systems, the Bacteroides fragilis type III CRISPR system was recently shown to produce a novel signal molecule, SAM-AMP, by conjugating ATP and SAM. SAM-AMP regulates a membrane effector of the CorA family to provide immunity. Here, we focus on NYN, a ribonuclease encoded within this system, probing its potential involvement in crRNA maturation. Structural modelling and in vitro ribonuclease assays reveal that NYN displays robust sequence-nonspecific, Mn2+-dependent ssRNA-cleavage activity. Our findings suggest a role for NYN in trimming crRNA intermediates into mature crRNAs, which is necessary for type III CRISPR antiviral defence. This study sheds light on the functional relevance of CRISPR-associated NYN proteins and highlights the complexity of CRISPR-mediated defence strategies in bacteria.
CRISPR-Cas 系统赋予原核生物适应性免疫,促进对入侵核酸的识别和破坏。III 型 CRISPR 系统由大型、多亚基核糖核蛋白复合物组成,具有催化 Cas10 亚基。当检测到外来 RNA 时,Cas10 会产生核苷酸信号分子,通过激活辅助效应蛋白引发免疫反应。在这些系统中,最近的研究表明,脆弱拟杆菌 III 型 CRISPR 系统通过将 ATP 和 SAM 缀合产生一种新型信号分子 SAM-AMP。SAM-AMP 调节 CorA 家族的膜效应子以提供免疫。在这里,我们专注于该系统中编码的核糖核酸酶 NYN,探究其在 crRNA 成熟过程中的潜在作用。结构建模和体外核糖核酸酶测定表明,NYN 具有强大的序列非特异性、Mn2+依赖性 ssRNA 切割活性。我们的研究结果表明 NYN 在将 crRNA 中间体修剪成成熟的 crRNA 中起作用,这对于 III 型 CRISPR 抗病毒防御是必要的。本研究揭示了 CRISPR 相关 NYN 蛋白的功能相关性,并强调了细菌中 CRISPR 介导防御策略的复杂性。