Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Department of Earth and Planetary Sciences, University of California, Berkeley, CA 94720, USA.
Science. 2018 Nov 16;362(6416):839-842. doi: 10.1126/science.aav4294. Epub 2018 Oct 18.
CRISPR-Cas systems provide microbes with adaptive immunity to infectious nucleic acids and are widely employed as genome editing tools. These tools use RNA-guided Cas proteins whose large size (950 to 1400 amino acids) has been considered essential to their specific DNA- or RNA-targeting activities. Here we present a set of CRISPR-Cas systems from uncultivated archaea that contain Cas14, a family of exceptionally compact RNA-guided nucleases (400 to 700 amino acids). Despite their small size, Cas14 proteins are capable of targeted single-stranded DNA (ssDNA) cleavage without restrictive sequence requirements. Moreover, target recognition by Cas14 triggers nonspecific cutting of ssDNA molecules, an activity that enables high-fidelity single-nucleotide polymorphism genotyping (Cas14-DETECTR). Metagenomic data show that multiple CRISPR-Cas14 systems evolved independently and suggest a potential evolutionary origin of single-effector CRISPR-based adaptive immunity.
CRISPR-Cas 系统为微生物提供了对传染性核酸的适应性免疫,被广泛用作基因组编辑工具。这些工具使用 RNA 指导的 Cas 蛋白,其较大的尺寸(950 到 1400 个氨基酸)被认为对其特定的 DNA 或 RNA 靶向活性至关重要。在这里,我们展示了一组来自未培养古菌的 CRISPR-Cas 系统,其中包含 Cas14,这是一组异常紧凑的 RNA 指导的核酸酶(400 到 700 个氨基酸)。尽管它们的体积很小,但 Cas14 蛋白能够在没有限制性序列要求的情况下靶向单链 DNA(ssDNA)切割。此外,Cas14 对靶标的识别触发了 ssDNA 分子的非特异性切割,这种活性使高保真单核苷酸多态性基因分型(Cas14-DETECTR)成为可能。宏基因组数据表明,多个 CRISPR-Cas14 系统独立进化,并暗示了基于单效应物的 CRISPR 适应性免疫的潜在进化起源。