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高密度向导 RNA 平铺和机器学习在 sp. PCC 7002 中设计 CRISPR 干扰。

High-Density Guide RNA Tiling and Machine Learning for Designing CRISPR Interference in sp. PCC 7002.

机构信息

Molecular and Microbiology, Sandia National Laboratories, P.O. Box 5800, MS 1413, Albuquerque, New Mexico 87185, United States.

Systems Biology, Sandia National Laboratories, P.O. Box 969, MS 9292, Livermore, California 94551, United States.

出版信息

ACS Synth Biol. 2023 Apr 21;12(4):1175-1186. doi: 10.1021/acssynbio.2c00653. Epub 2023 Mar 9.

Abstract

While CRISPRi was previously established in sp. PCC 7002 (hereafter 7002), the design principles for guide RNA (gRNA) effectiveness remain largely unknown. Here, 76 strains of 7002 were constructed with gRNAs targeting three reporter systems to evaluate features that impact gRNA efficiency. Correlation analysis of the data revealed that important features of gRNA design include the position relative to the start codon, GC content, protospacer adjacent motif (PAM) site, minimum free energy, and targeted DNA strand. Unexpectedly, some gRNAs targeting upstream of the promoter region showed small but significant increases in reporter expression, and gRNAs targeting the terminator region showed greater repression than gRNAs targeting the 3' end of the coding sequence. Machine learning algorithms enabled prediction of gRNA effectiveness, with Random Forest having the best performance across all training sets. This study demonstrates that high-density gRNA data and machine learning can improve gRNA design for tuning gene expression in 7002.

摘要

尽管 CRISPRi 先前已在 sp. PCC 7002(以下简称 7002)中建立,但指导 RNA(gRNA)有效性的设计原则在很大程度上仍不清楚。在这里,构建了 76 株靶向三个报告系统的 gRNA 的 7002 菌株,以评估影响 gRNA 效率的特征。数据分析的相关性分析表明,gRNA 设计的重要特征包括相对于起始密码子的位置、GC 含量、前导间隔基序(PAM)位点、最小自由能和靶向 DNA 链。出乎意料的是,一些靶向启动子区域上游的 gRNA 表现出微小但显著的报告基因表达增加,而靶向终止子区域的 gRNA 比靶向编码序列 3'端的 gRNA 具有更强的抑制作用。机器学习算法能够预测 gRNA 的有效性,其中随机森林在所有训练集中的性能最佳。这项研究表明,高密度 gRNA 数据和机器学习可以改进 7002 中基因表达的 gRNA 设计。

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