Suppr超能文献

一个本科实验室模块,该模块使用CRISPR/Cas9系统在酵母中产生移码突变。

An undergraduate laboratory module that uses the CRISPR/Cas9 system to generate frameshift mutations in yeast.

作者信息

de Waal Eric, Tran Thomas, Abbondanza Domenic, Dey Arup, Peterson Celeste

机构信息

Biology Department, Suffolk University, Boston, Massachusetts.

Department of Biochemistry and Molecular Biology, University of Massachusetts Amherst, Amherst, Massachusetts.

出版信息

Biochem Mol Biol Educ. 2019 Sep;47(5):573-580. doi: 10.1002/bmb.21280. Epub 2019 Jun 21.

Abstract

The CRISPR/Cas9 system is a powerful tool for gene editing and it has become increasingly important for biology students to understand this emerging technique. Most CRISPR laboratory teaching modules use complex metazoan systems or mammalian cell culture which can be expensive. Here, we present a lab module that engages students in learning the fundamentals of CRISPR/Cas9 methodology using the simple and inexpensive model system, Saccharomyces cerevisiae. Students use CRISPR/Cas9 and nonhomologous end joining to generate frameshift insertion and deletion mutations in the CAN1 gene, which are easily selected for using media plates that have canavanine. DNA sequencing is also performed to determine what type of mutation occurred in gene-edited cells. This easy to implement set of experiments has been run as both a 5-week and a shorter 3-week lab module. Learning assessments demonstrate increased understanding in CRISPR-related concepts as well as increased confidence using molecular techniques. Thus, this CRISPR/Cas9 lab module can be added to an existing Genetics, Microbiology, or Molecular Biology lab course to help undergraduate students learn current gene editing techniques with limited effort and cost. © 2019 International Union of Biochemistry and Molecular Biology, 47(5):573-580, 2019.

摘要

CRISPR/Cas9系统是一种强大的基因编辑工具,对于生物学专业的学生来说,理解这一新兴技术变得越来越重要。大多数CRISPR实验室教学模块使用复杂的后生动物系统或哺乳动物细胞培养,成本可能很高。在此,我们展示了一个实验模块,让学生使用简单且成本低廉的酿酒酵母模型系统来学习CRISPR/Cas9方法的基本原理。学生使用CRISPR/Cas9和非同源末端连接在CAN1基因中产生移码插入和缺失突变,通过含有刀豆氨酸的培养基平板可以轻松筛选出这些突变。还进行DNA测序以确定基因编辑细胞中发生了何种类型的突变。这套易于实施的实验既可以作为一个为期5周的实验模块,也可以作为一个较短的为期3周的实验模块来开展。学习评估表明,学生对CRISPR相关概念的理解有所增强,并且使用分子技术的信心也有所提高。因此,这个CRISPR/Cas9实验模块可以添加到现有的遗传学、微生物学或分子生物学实验课程中,以帮助本科生以有限的精力和成本学习当前的基因编辑技术。© 2019国际生物化学与分子生物学联盟,47(5):573 - 580,2019。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验