Single-molecule analysis of mtDNA replication with high resolution

被引:1
|
作者
Tigano, Marco [1 ]
Phillips, Aaron Fraser [1 ,2 ]
Sfeir, Agnel [1 ]
机构
[1] NYU, Sch Med, Skirball Inst Biomol Med, Dept Dev Genet, New York, NY 10012 USA
[2] Inzen Therapeut, New York, NY USA
来源
MITOCHONDRIA, 3RD EDITION | 2020年 / 155卷
关键词
D O I
10.1016/bs.mcb.2019.10.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
DNA combing technology is a powerful methodology for the study of DNA replication in vivo. This tool can be used to identify origins of replication, assess of directionality of forks, and measure fork speed. Over the years, the method has been used extensively to study nuclear DNA replication. The first step involves the incorporation of thymidine analogs (CldU and IdU) into nascent DNA chains and followed by their visualization with immunofluorescence using antibodies that can distinguish the two analogs. Recently, we adapted and fine-tuned DNA combing technology to the specifics of mitochondrial DNA (Phillips et al., 2017, p. 155). The protocol, which we termed mito-SMARD (mitochondrial single molecule analysis of replication DNA), provides in vivo insight intomitochondrial DNA(mtDNA) replication with high resolution.
引用
收藏
页码:401 / 414
页数:14
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