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非模式生物基因组编辑的路线图与注意事项:遗传变异与脱靶分析

Roadmap and Considerations for Genome Editing in a Non-Model Organism: Genetic Variations and Off-Target Profiling.

作者信息

Wattad Hanin, Molcho Jonathan, Manor Rivka, Weil Simy, Aflalo Eliahu D, Chalifa-Caspi Vered, Sagi Amir

机构信息

Department of Life Sciences, Ben-Gurion University of the Negev, P.O. Box 653, Beer-Sheva 8410501, Israel.

The National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, P.O. Box 653, Beer-Sheva 8410501, Israel.

出版信息

Int J Mol Sci. 2024 Nov 22;25(23):12530. doi: 10.3390/ijms252312530.

Abstract

The CRISPR/Cas genome editing approach in non-model organisms poses challenges that remain to be resolved. Here, we demonstrated a generalized roadmap for a de novo genome annotation approach applied to the non-model organism . We also addressed the typical genome editing challenges arising from genetic variations, such as a high frequency of single nucleotide polymorphisms, differences in sex chromosomes, and repetitive sequences that can lead to off-target events. For the genome editing of , our laboratory recently adapted the CRISPR/Cas genome editing approach to embryos and the embryonic primary cell culture. In this continuation study, an annotation pipeline was trained to predict the gene models by leveraging the available genomic, transcriptomic, and proteomic data, and enabling accurate gene prediction and guide design for knock-outs. A next-generation sequencing analysis demonstrated a high frequency of genetic variations in genes on both autosomal and sex chromosomes, which have been shown to affect the accuracy of editing analyses. To enable future applications based on the CRISPR/Cas tool in non-model organisms, we also verified the reliability of editing efficiency and tracked off-target frequencies. Despite the lack of comprehensive information on non-model organisms, this study provides an example of the feasibility of selecting and editing specific genes with a high degree of certainty.

摘要

在非模式生物中应用CRISPR/Cas基因组编辑方法存在一些尚待解决的挑战。在此,我们展示了一种适用于非模式生物的从头基因组注释方法的通用路线图。我们还解决了由遗传变异引发的典型基因组编辑挑战,例如单核苷酸多态性的高频率、性染色体差异以及可能导致脱靶事件的重复序列。对于[具体生物名称未给出]的基因组编辑,我们实验室最近将CRISPR/Cas基因组编辑方法应用于胚胎和胚胎原代细胞培养。在这项后续研究中,通过利用可用的基因组、转录组和蛋白质组数据,训练了一个注释流程来预测基因模型,并实现准确的基因预测和用于基因敲除的向导设计。下一代测序分析表明,常染色体和性染色体上的基因均存在高频率的遗传变异,这些变异已被证明会影响编辑分析的准确性。为了使基于CRISPR/Cas工具在非模式生物中的未来应用成为可能,我们还验证了编辑效率的可靠性并追踪了脱靶频率。尽管缺乏关于非模式生物的全面信息,但本研究提供了一个以高度确定性选择和编辑特定基因的可行性示例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2492/11641748/664ee80c254d/ijms-25-12530-g001.jpg

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