Xiao Yibei, Ng Sherwin, Nam Ki Hyun, Ke Ailong
Department of Molecular Biology and Genetics, Cornell University, 253 Biotechnology Building, Ithaca, New York 14853, USA.
Pohang Accelerator Laboratory, Pohang University of Science and Technology, Pohang, South Korea.
Nature. 2017 Oct 5;550(7674):137-141. doi: 10.1038/nature24020. Epub 2017 Sep 4.
CRISPR (clustered regularly interspaced short palindromic repeats) and the nearby Cas (CRISPR-associated) operon establish an RNA-based adaptive immunity system in prokaryotes. Molecular memory is created when a short foreign DNA-derived prespacer is integrated into the CRISPR array as a new spacer. Whereas the RNA-guided CRISPR interference mechanism varies widely among CRISPR-Cas systems, the spacer integration mechanism is essentially identical. The conserved Cas1 and Cas2 proteins form an integrase complex consisting of two distal Cas1 dimers bridged by a Cas2 dimer. The prespacer is bound by Cas1-Cas2 as a dual-forked DNA, and the terminal 3'-OH of each 3' overhang serves as an attacking nucleophile during integration. The prespacer is preferentially integrated into the leader-proximal region of the CRISPR array, guided by the leader sequence and a pair of inverted repeats inside the CRISPR repeat. Spacer integration in the well-studied Escherichia coli type I-E CRISPR system also relies on the bacterial integration host factor. In type II-A CRISPR, however, Cas1-Cas2 alone integrates spacers efficiently in vitro; other Cas proteins (such as Cas9 and Csn2) have accessory roles in the biogenesis phase of prespacers. Here we present four structural snapshots from the type II-A system of Enterococcus faecalis Cas1 and Cas2 during spacer integration. Enterococcus faecalis Cas1-Cas2 selectively binds to a splayed 30-base-pair prespacer bearing 4-nucleotide 3' overhangs. Three molecular events take place upon encountering a target: first, the Cas1-Cas2-prespacer complex searches for half-sites stochastically, then it preferentially interacts with the leader-side CRISPR repeat, and finally, it catalyses a nucleophilic attack that connects one strand of the leader-proximal repeat to the prespacer 3' overhang. Recognition of the spacer half-site requires DNA bending and leads to full integration. We derive a mechanistic framework to explain the stepwise spacer integration process and the leader-proximal preference.
CRISPR(成簇规律间隔短回文重复序列)及其附近的Cas(CRISPR相关)操纵子在原核生物中建立了一种基于RNA的适应性免疫系统。当一段源自外源DNA的短前间隔序列作为新的间隔序列整合到CRISPR阵列中时,分子记忆便得以形成。虽然RNA引导的CRISPR干扰机制在不同的CRISPR-Cas系统中差异很大,但间隔序列整合机制基本相同。保守的Cas1和Cas2蛋白形成一个整合酶复合体,该复合体由两个由Cas2二聚体桥接的远端Cas1二聚体组成。前间隔序列以双叉DNA的形式与Cas1-Cas2结合,每个3'端突出端的末端3'-OH在整合过程中作为进攻性亲核试剂。在前导序列和CRISPR重复序列内的一对反向重复序列的引导下,前间隔序列优先整合到CRISPR阵列的前导序列近端区域。在经过充分研究的大肠杆菌I-E型CRISPR系统中,间隔序列的整合也依赖于细菌整合宿主因子。然而,在II-A型CRISPR中,Cas1-Cas2单独就能在体外高效地整合间隔序列;其他Cas蛋白(如Cas9和Csn2)在前间隔序列生物合成阶段起辅助作用。在这里,我们展示了粪肠球菌Cas1和Cas2在II-A型系统间隔序列整合过程中的四个结构快照。粪肠球菌Cas1-Cas2选择性地结合到一个带有4个核苷酸3'端突出端的展开的30碱基对前间隔序列上。遇到靶标时会发生三个分子事件:首先,Cas1-Cas2-前间隔序列复合体随机搜索半位点,然后它优先与前导序列侧的CRISPR重复序列相互作用,最后,它催化亲核攻击,将前导序列近端重复序列的一条链与前间隔序列的3'端突出端连接起来。间隔序列半位点的识别需要DNA弯曲,并导致完全整合。我们推导了一个机制框架来解释间隔序列逐步整合过程以及前导序列近端偏好性。