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通过 CRISPR/Cas9 靶向编辑菱形藻核编码质体蛋白。

Targeted Gene Editing of Nuclear-Encoded Plastid Proteins in Phaeodactylum tricornutum via CRISPR/Cas9.

机构信息

Laboratoire de Physiologie Cellulaire et Végétale, CNRS, CEA, INRAE, Univ. Grenoble Alpes, IRIG, CEA Grenoble, Grenoble, France.

出版信息

Methods Mol Biol. 2024;2776:269-287. doi: 10.1007/978-1-0716-3726-5_17.

Abstract

Genome modifications in microalgae have emerged as a crucial and indispensable tool for research in fundamental and applied biology. In particular, CRISPR/Cas9 has gained significant recognition as a highly effective method for genome engineering in these photosynthetic organisms, enabling the targeted induction of mutations in specific regions of the genome. Here, we present a comprehensive protocol for generating knock-out mutants in the model diatom Phaeodactylum tricornutum using CRISPR/Cas9 by both biolistic transformation and bacterial conjugation. Our protocol outlines the step-by-step procedures and experimental conditions required to achieve successful genome editing, including the design and construction of guide RNAs, the delivery of CRISPR/Cas9 components into the algae cells, and the selection of the generated knockout mutants. Through the implementation of this protocol, researchers can harness the potential of CRISPR/Cas9 in P. tricornutum to advance the understanding of diatom biology and explore their potential applications in various fields.

摘要

在基础和应用生物学研究中,藻类基因组修饰已成为一项至关重要且不可或缺的工具。特别是 CRISPR/Cas9 已被广泛认可为一种在这些光合生物中进行基因组工程的高效方法,可以靶向诱导基因组特定区域的突变。在这里,我们通过生物弹道转化和细菌接合两种方法,提供了一种利用 CRISPR/Cas9 在模式硅藻三角褐指藻中产生敲除突变体的综合方案。本方案概述了实现成功基因组编辑所需的逐步程序和实验条件,包括 guide RNA 的设计和构建、CRISPR/Cas9 组件递送入藻类细胞,以及生成的敲除突变体的筛选。通过实施本方案,研究人员可以利用 CRISPR/Cas9 在三角褐指藻中的潜力,推进对硅藻生物学的理解,并探索其在各个领域的潜在应用。

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