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Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery

机译:通过I-FCRISPR-Cas系统获取外源DNA需要干扰机器的所有组件

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摘要

CRISPR immunity depends on acquisition of fragments of foreign DNA into CRISPR arrays. For type I-E CRISPR–Cas systems two modes of spacer acquisition, naïve and primed adaptation, were described. Naïve adaptation requires just two most conserved Cas1 and Cas2 proteins; it leads to spacer acquisition from both foreign and bacterial DNA and results in multiple spacers incapable of immune response. Primed adaptation requires all Cas proteins and a CRISPR RNA recognizing a partially matching target. It leads to selective acquisition of spacers from DNA molecules recognized by priming CRISPR RNA, with most spacers capable of protecting the host. Here, we studied spacer acquisition by a type I-F CRISPR–Cas system. We observe both naïve and primed adaptation. Both processes require not just Cas1 and Cas2, but also intact Csy complex and CRISPR RNA. Primed adaptation shows a gradient of acquisition efficiency as a function of distance from the priming site and a strand bias that is consistent with existence of single-stranded adaption intermediates. The results provide new insights into the mechanism of spacer acquisition and illustrate surprising mechanistic diversity of related CRISPR–Cas systems.
机译:CRISPR免疫力取决于将外源DNA片段采集到CRISPR阵列中的能力。对于I-E型CRISPR-Cas系统,描述了两种间隔区获取模式:天真和引发适应。幼稚的适应只需要两个最保守的Cas1和Cas2蛋白;它导致从外源和细菌DNA中获得间隔子,并导致多个间隔子无法免疫反应。启动适应需要所有Cas蛋白和CRISPR RNA识别部分匹配的靶标。它导致从通过引发CRISPR RNA识别的DNA分子中选择性地获得间隔子,而大多数间隔子都能够保护宿主。在这里,我们研究了通过I-F CRISPR–Cas系统获取间隔区。我们观察到幼稚的和适应性的适应。这两个过程不仅需要Cas1和Cas2,还需要完整的Csy复合体和CRISPR RNA。引发的适应性显示获取效率的梯度是与引发部位的距离的函数以及与单链适应性中间体的存在一致的链偏向。结果提供了对间隔物获取机制的新见解,并说明了相关CRISPR–Cas系统令人惊讶的机制多样性。

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