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基因靶向技术:利用工程化序列特异性核酸酶的潜在应用于作物改良。

Gene Targeting Facilitated by Engineered Sequence-Specific Nucleases: Potential Applications for Crop Improvement.

机构信息

Shanghai Center for Plant Stress Biology and Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Plant Cell Physiol. 2021 Oct 1;62(5):752-765. doi: 10.1093/pcp/pcab034.

Abstract

Humans are currently facing the problem of how to ensure that there is enough food to feed all of the world's population. Ensuring that the food supply is sufficient will likely require the modification of crop genomes to improve their agronomic traits. The development of engineered sequence-specific nucleases (SSNs) paved the way for targeted gene editing in organisms, including plants. SSNs generate a double-strand break (DSB) at the target DNA site in a sequence-specific manner. These DSBs are predominantly repaired via error-prone non-homologous end joining and are only rarely repaired via error-free homology-directed repair if an appropriate donor template is provided. Gene targeting (GT), i.e. the integration or replacement of a particular sequence, can be achieved with combinations of SSNs and repair donor templates. Although its efficiency is extremely low, GT has been achieved in some higher plants. Here, we provide an overview of SSN-facilitated GT in higher plants and discuss the potential of GT as a powerful tool for generating crop plants with desirable features.

摘要

人类目前正面临着如何确保有足够的食物来养活全世界人口的问题。确保粮食供应充足可能需要对作物基因组进行修饰,以改善其农艺性状。工程化序列特异性核酸酶(SSNs)的发展为包括植物在内的生物体的靶向基因编辑铺平了道路。SSNs 以序列特异性的方式在靶 DNA 位点产生双链断裂(DSB)。这些 DSB 主要通过易错的非同源末端连接修复,只有在提供适当的供体模板时才很少通过无错误的同源定向修复修复。基因靶向(GT),即特定序列的整合或替换,可以通过 SSNs 和修复供体模板的组合来实现。尽管其效率极低,但在一些高等植物中已经实现了 GT。在这里,我们提供了 SSN 介导的高等植物 GT 的概述,并讨论了 GT 作为一种生成具有理想特性的作物植物的强大工具的潜力。

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