DNA
DNA修复
生物
计算生物学
基因组
基因组编辑
基因组工程
序列(生物学)
遗传学
DNA损伤
DNA测序
基因
作者
Qiudeng Que,Zhongying Chen,Tim Kelliher,David S. Skibbe,Shiqi Dong,Mary-Dell Chilton
出处
期刊:Methods in molecular biology
日期:2019-01-01
卷期号:: 3-24
被引量:16
标识
DOI:10.1007/978-1-4939-8991-1_1
摘要
Remarkable progress in the development of technologies for sequence-specific modification of primary DNA sequences has enabled the precise engineering of crops with novel characteristics. These programmable sequence-specific modifiers include site-directed nucleases (SDNs) and base editors (BEs). Currently, these genome editing machineries can be targeted to specific chromosomal locations to induce sequence changes. However, the sequence mutation outcomes are often greatly influenced by the type of DNA damage being generated, the status of host DNA repair machinery, and the presence and structure of DNA repair donor molecule. The outcome of sequence modification from repair of DNA double-strand breaks (DSBs) is often uncontrollable, resulting in unpredictable sequence insertions or deletions of various sizes. For base editing, the precision of intended edits is much higher, but the efficiency can vary greatly depending on the type of BE used or the activity of the endogenous DNA repair systems. This article will briefly review the possible DNA repair pathways present in the plant cells commonly used for generating edited variants for genome engineering applications. We will discuss the potential use of DNA repair mechanisms for developing and improving methodologies to enhance genome engineering efficiency and to direct DNA repair processes toward the desired outcomes.
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