CRISPR-Mediated Gene Editing: Scientific and Ethical Issues

清脆的 基因组编辑 回文 核糖核酸 效应器 生物 转录激活物样效应核酸酶 遗传学 DNA 计算生物学 RNA编辑 基因组 Cas9 抄写(语言学) 基因 细胞生物学 哲学 语言学
作者
Jarrod Bailey
出处
期刊:Trends in Biotechnology [Elsevier]
卷期号:37 (9): 920-921 被引量:6
标识
DOI:10.1016/j.tibtech.2019.05.002
摘要

There remains substantial evidence to warrant great concern over the poor efficiency and specificity of clustered regularly interspaced short palindromic repeats (CRISPR)-mediated genetic modification (GM), despite relatively minor improvements compared to other GM methods. These issues cause persistent, adverse, ethical, and scientific consequences for GM animals, which may never be sufficiently resolvable. There remains substantial evidence to warrant great concern over the poor efficiency and specificity of clustered regularly interspaced short palindromic repeats (CRISPR)-mediated genetic modification (GM), despite relatively minor improvements compared to other GM methods. These issues cause persistent, adverse, ethical, and scientific consequences for GM animals, which may never be sufficiently resolvable. Improving CRISPR Genome Editing by Engineering Guide RNAsMoon et al.Trends in BiotechnologyMarch 4, 2019In BriefCRISPR technology is a two-component gene editing system in which the effector protein induces genetic alterations with the aid of a gene targeting guide RNA. Guide RNA can be produced through chemical synthesis, in vitro transcription, or intracellular transcription. Guide RNAs can be engineered to have chemical modifications, alterations in the spacer length, sequence modifications, fusion of RNA or DNA components, and incorporation of deoxynucleotides. Engineered guide RNA can improve genome editing efficiency and target specificity, regulation of biological toxicity, sensitive and specific molecular imaging, multiplexing, and editing flexibility. Full-Text PDF
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