Jones Daniel Lawson, Leroy Prune, Unoson Cecilia, Fange David, Ćurić Vladimir, Lawson Michael J, Elf Johan
Department of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Science. 2017 Sep 29;357(6358):1420-1424. doi: 10.1126/science.aah7084. Epub 2017 Sep 28.
How fast can a cell locate a specific chromosomal DNA sequence specified by a single-stranded oligonucleotide? To address this question, we investigate the intracellular search processes of the Cas9 protein, which can be programmed by a guide RNA to bind essentially any DNA sequence. This targeting flexibility requires Cas9 to unwind the DNA double helix to test for correct base pairing to the guide RNA. Here we study the search mechanisms of the catalytically inactive Cas9 (dCas9) in living by combining single-molecule fluorescence microscopy and bulk restriction-protection assays. We find that it takes a single fluorescently labeled dCas9 6 hours to find the correct target sequence, which implies that each potential target is bound for less than 30 milliseconds. Once bound, dCas9 remains associated until replication. To achieve fast targeting, both Cas9 and its guide RNA have to be present at high concentrations.
细胞能多快找到由单链寡核苷酸指定的特定染色体DNA序列?为了解决这个问题,我们研究了Cas9蛋白的细胞内搜索过程,它可以由引导RNA编程以结合基本上任何DNA序列。这种靶向灵活性要求Cas9解开DNA双螺旋以测试与引导RNA的正确碱基配对。在这里,我们通过结合单分子荧光显微镜和大量限制保护试验,研究了催化失活的Cas9(dCas9)在活细胞中的搜索机制。我们发现,单个荧光标记的dCas9需要6小时才能找到正确的靶序列,这意味着每个潜在靶点的结合时间不到30毫秒。一旦结合,dCas9会一直保持结合状态直到复制。为了实现快速靶向,Cas9及其引导RNA都必须以高浓度存在。