Department of Microbiology and Immunology, Montana State University, Bozeman, MT 59717, USA.
Department of Microbiology and Immunology, Montana State University, Bozeman, MT 59717, USA.
Curr Biol. 2021 Aug 23;31(16):3515-3524.e6. doi: 10.1016/j.cub.2021.05.068. Epub 2021 Jun 25.
CRISPR-associated proteins (Cas1 and Cas2) integrate foreign DNA at the "leader" end of CRISPR loci. Several CRISPR leader sequences are reported to contain a binding site for a DNA-bending protein called integration host factor (IHF). IHF-induced DNA bending kinks the leader of type I-E CRISPRs, recruiting an upstream sequence motif that helps dock Cas1-2 onto the first repeat of the CRISPR locus. To determine the prevalence of IHF-directed CRISPR adaptation, we analyzed 15,274 bacterial and archaeal CRISPR leaders. These experiments reveal multiple IHF binding sites and diverse upstream sequence motifs in a subset of the I-C, I-E, I-F, and II-C CRISPR leaders. We identify subtype-specific motifs and show that the phase of these motifs is critical for CRISPR adaptation. Collectively, this work clarifies the prevalence and mechanism(s) of IHF-dependent CRISPR adaptation and suggests that leader sequences and adaptation proteins may coevolve under the selective pressures of foreign genetic elements like plasmids or phages.
CRISPR 相关蛋白(Cas1 和 Cas2)将外源 DNA 整合到 CRISPR 基因座的“前导”端。据报道,几个 CRISPR 前导序列包含一个结合蛋白整合宿主因子(IHF)的结合位点。IHF 诱导的 DNA 弯曲使 I 型-E CRISPR 的前导弯曲,募集一个上游序列基序,帮助 Cas1-2 停靠在 CRISPR 基因座的第一个重复序列上。为了确定 IHF 指导的 CRISPR 适应的普遍性,我们分析了 15274 个细菌和古菌的 CRISPR 前导序列。这些实验在 I-C、I-E、I-F 和 II-C CRISPR 前导序列的一个亚组中揭示了多个 IHF 结合位点和不同的上游序列基序。我们确定了亚型特异性基序,并表明这些基序的相位对于 CRISPR 适应至关重要。总的来说,这项工作阐明了 IHF 依赖的 CRISPR 适应的普遍性和机制,并表明前导序列和适应蛋白可能在外源遗传元件(如质粒或噬菌体)的选择压力下共同进化。