Department of Biochemistry, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada, N6A 5C1.
Department of Microbiology, University of Manitoba, Winnipeg, MB, Canada R3T 2N2.
Nucleic Acids Res. 2018 Dec 14;46(22):11990-12007. doi: 10.1093/nar/gky976.
LAGLIDADG homing endonucleases (meganucleases) are site-specific mobile endonucleases that can be adapted for genome-editing applications. However, one problem when reprogramming meganucleases on non-native substrates is indirect readout of DNA shape and flexibility at the central 4 bases where cleavage occurs. To understand how the meganuclease active site regulates DNA cleavage, we used functional selections and deep sequencing to profile the fitness landscape of 1600 I-LtrI and I-OnuI active site variants individually challenged with 67 substrates with central 4 base substitutions. The wild-type active site was not optimal for cleavage on many substrates, including the native I-LtrI and I-OnuI targets. Novel combinations of active site residues not observed in known meganucleases supported activity on substrates poorly cleaved by the wild-type enzymes. Strikingly, combinations of E or D substitutions in the two metal-binding residues greatly influenced cleavage activity, and E184D variants had a broadened cleavage profile. Analyses of I-LtrI E184D and the wild-type proteins co-crystallized with the non-cognate AACC central 4 sequence revealed structural differences that correlated with kinetic constants for cleavage of individual DNA strands. Optimizing meganuclease active sites to enhance cleavage of non-native central 4 target sites is a straightforward addition to engineering workflows that will expand genome-editing applications.
LAGLIDADG 归巢内切核酸酶(meganucleases)是一种具有序列特异性的可移动内切核酸酶,可用于基因组编辑应用。然而,在非天然底物上重新编程 meganucleases 时存在一个问题,即无法直接读取发生切割的中央 4 个碱基处的 DNA 形状和灵活性。为了了解 meganuclease 活性位点如何调节 DNA 切割,我们使用功能选择和深度测序来分析 1600 个 I-LtrI 和 I-OnuI 活性位点变体在 67 个具有中央 4 个碱基取代的底物上的适应性景观。野生型活性位点在许多底物上的切割并不理想,包括天然的 I-LtrI 和 I-OnuI 靶标。在已知的 meganuclease 中未观察到的新型活性位点残基组合支持对野生型酶难以切割的底物的活性。引人注目的是,两个金属结合残基中的 E 或 D 取代的组合极大地影响了切割活性,并且 E184D 变体具有更广泛的切割谱。对 I-LtrI E184D 和野生型蛋白与非同源 AACC 中央 4 序列共结晶的分析揭示了与单个 DNA 链切割的动力学常数相关的结构差异。优化 meganuclease 活性位点以增强非天然中央 4 靶位点的切割是工程工作流程的一个简单附加项,将扩展基因组编辑应用。