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内源性细胞过程对靶向基因修复的调控。

Regulation of targeted gene repair by intrinsic cellular processes.

作者信息

Engstrom Julia U, Suzuki Takayuki, Kmiec Eric B

机构信息

University of Delaware, Department of Biological Sciences, Newark, DE 19716, USA.

出版信息

Bioessays. 2009 Feb;31(2):159-68. doi: 10.1002/bies.200800119.

Abstract

Targeted gene alteration (TGA) is a strategy for correcting single base mutations in the DNA of human cells that cause inherited disorders. TGA aims to reverse a phenotype by repairing the mutant base within the chromosome itself, avoiding the introduction of exogenous genes. The process of how to accurately repair a genetic mutation is elucidated through the use of single-stranded DNA oligonucleotides (ODNs) that can enter the cell and migrate to the nucleus. These specifically designed ODNs hybridize to the target sequence and act as a beacon for nucleotide exchange. The key to this reaction is the frequency with which the base is corrected; this will determine whether the approach becomes clinically relevant or not. Over the course of the last five years, workers have been uncovering the role played by the cells in regulating the gene repair process. In this essay, we discuss how the impact of the cell on TGA has evolved through the years and illustrate ways that inherent cellular pathways could be used to enhance TGA activity. We also describe the cost to cell metabolism and survival when certain processes are altered to achieve a higher frequency of repair.

摘要

靶向基因改造(TGA)是一种纠正人类细胞DNA中导致遗传性疾病的单碱基突变的策略。TGA旨在通过修复染色体自身内的突变碱基来逆转表型,避免引入外源基因。通过使用能够进入细胞并迁移至细胞核的单链DNA寡核苷酸(ODN),阐明了如何精确修复基因突变的过程。这些经过特殊设计的ODN与靶序列杂交,并作为核苷酸交换的信号。该反应的关键在于碱基被纠正的频率;这将决定该方法是否具有临床相关性。在过去五年中,研究人员一直在揭示细胞在调节基因修复过程中所起的作用。在本文中,我们讨论了多年来细胞对TGA的影响是如何演变的,并举例说明了如何利用固有的细胞途径来增强TGA活性。我们还描述了为实现更高的修复频率而改变某些过程时,细胞代谢和生存所付出的代价。

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