Laboratory of Bacteriology, The Rockefeller University, New York, NY, USA.
Nat Rev Microbiol. 2019 Jan;17(1):7-12. doi: 10.1038/s41579-018-0071-7.
Many bacteria and archaea have the unique ability to heritably alter their genomes by incorporating small fragments of foreign DNA, called spacers, into CRISPR loci. Once transcribed and processed into individual CRISPR RNAs, spacer sequences guide Cas effector nucleases to destroy complementary, invading nucleic acids. Collectively, these two processes are known as the CRISPR-Cas immune response. In this Progress article, we review recent studies that have advanced our understanding of the molecular mechanisms underlying spacer acquisition and that have revealed a fundamental link between the two phases of CRISPR immunity that ensures optimal immunity from newly acquired spacers. Finally, we highlight important open questions and discuss the potential basic and applied impact of spacer acquisition research.
许多细菌和古菌具有通过将称为间隔序列的小片段外源 DNA 整合到 CRISPR 基因座中来遗传地改变其基因组的独特能力。一旦被转录并加工成单个 CRISPR RNA,间隔序列就会引导 Cas 效应核酸酶破坏互补的入侵核酸。这两个过程统称为 CRISPR-Cas 免疫反应。在这篇进展文章中,我们回顾了最近的研究,这些研究增进了我们对间隔序列获取的分子机制的理解,并揭示了 CRISPR 免疫的两个阶段之间的基本联系,从而确保了从新获得的间隔序列中获得最佳的免疫效果。最后,我们强调了重要的未解决问题,并讨论了间隔序列获取研究的潜在基础和应用影响。