一个教育模块,探索CRISPR技术与无细胞转录翻译系统。

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS
Synthetic biology (Oxford, England) Pub Date : 2019-01-21 eCollection Date: 2019-01-01 DOI:10.1093/synbio/ysz005
Daphne Collias, Ryan Marshall, Scott P Collins, Chase L Beisel, Vincent Noireaux
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引用次数: 24

摘要

在过去的6年里,CRISPR-Cas系统已经从细菌和古细菌的适应性防御系统转变为革命性的基因组编辑工具。由此产生的CRISPR技术推动了治疗遗传疾病和根除人类害虫的创新,同时也引发了关于人类生殖细胞和农作物基因编辑的社会问题。因此,将CRISPR引入课堂提供了一种让学生接触尖端技术的手段,并促进了对科学与社会交叉领域伦理问题的讨论。然而,在课堂环境中使用这些技术一直很困难,因为典型的实验依赖于细胞系统,如细菌或哺乳动物细胞。我们最近报道了一种大肠杆菌无细胞转录-翻译(TXTL)系统的使用,该系统用更短的实验时间和有限的设备简化了CRISPR技术的演示和测试。在这里,我们描述了三个教育模块,旨在让本科生使用TXTL接触CRISPR技术。三个序列模块包括(i)设计引导DNA靶向的RNA, (ii)测量TXTL中的DNA切割活性,(iii)测试靶向序列或RNA骨干的突变如何影响DNA结合和切割。这些模块包括详细的协议,小组讨论或个人评估的问题,以及介绍CRISPR和TXTL的讲座幻灯片。我们希望这些模块能让学生在课堂上体验到CRISPR技术的力量和前景,并与他们的老师和同龄人一起讨论社会的机遇和潜在风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An educational module to explore CRISPR technologies with a cell-free transcription-translation system.

An educational module to explore CRISPR technologies with a cell-free transcription-translation system.

An educational module to explore CRISPR technologies with a cell-free transcription-translation system.

An educational module to explore CRISPR technologies with a cell-free transcription-translation system.

Within the last 6 years, CRISPR-Cas systems have transitioned from adaptive defense systems in bacteria and archaea to revolutionary genome-editing tools. The resulting CRISPR technologies have driven innovations for treating genetic diseases and eradicating human pests while raising societal questions about gene editing in human germline cells as well as crop plants. Bringing CRISPR into the classroom therefore offers a means to expose students to cutting edge technologies and to promote discussions about ethical questions at the intersection of science and society. However, working with these technologies in a classroom setting has been difficult because typical experiments rely on cellular systems such as bacteria or mammalian cells. We recently reported the use of an E. coli cell-free transcription-translation (TXTL) system that simplifies the demonstration and testing of CRISPR technologies with shorter experiments and limited equipment. Here, we describe three educational modules intended to expose undergraduate students to CRISPR technologies using TXTL. The three sequential modules comprise (i) designing the RNAs that guide DNA targeting, (ii) measuring DNA cleavage activity in TXTL and (iii) testing how mutations to the targeting sequence or RNA backbone impact DNA binding and cleavage. The modules include detailed protocols, questions for group discussions or individual evaluation, and lecture slides to introduce CRISPR and TXTL. We expect these modules to allow students to experience the power and promise of CRISPR technologies in the classroom and to engage with their instructor and peers about the opportunities and potential risks for society.

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