脑癌研究进展:通过单碱基编辑在 IDH1 中创建单倍单点突变。

Journal of oncology research and therapy Pub Date : 2019-01-01 Epub Date: 2018-10-03
Sagar R Shah, Alfredo Quinones-Hinojosa, Shuli Xia
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引用次数: 0

摘要

70% 的 II 级和 III 级胶质瘤、10% 的急性髓性白血病以及胆管癌、黑色素瘤和软骨肉瘤中都存在异柠檬酸脱氢酶 1(IDH1)基因突变。人们提出了许多机制来说明突变 IDH1 的生物功能。突变 IDH1 的大多数功能研究都是在 IDH1 野生型背景的外源过表达系统中进行的。这篇微型综述对 Wei 等人最近发表的论文进行了评论,其中采用了一种高效的 "单碱基编辑 "方法,在不诱导 IDH1 基因双链断裂的情况下产生了单并列 IDH1 R132H 突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advances in Brain Cancer: Creating Monoallelic Single Point Mutation in IDH1 by Single Base Editing.

Mutations in the Isocitrate Dehydrogenase 1 (IDH1) gene occur in 70% of grade II and grade III gliomas, 10% of acute myeloid leukemia, as well as cholangiocarcinomas, melanomas, and chondrosarcomas. Numerous mechanisms have been proposed to illustrate the biological function of mutant IDH1. Most functional studies of mutant IDH1 have been conducted in exogenous overexpression systems with the IDH1 wild type background. This mini-review comments on recent publication by Wei et al, in which a highly efficient "single base editing" approach was employed to generate monoallelic IDH1 R132H mutation without the induction of a double strand break in the IDH1 gene.

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