线粒体DNA
生物
基因组
DNA损伤
核DNA
DNA修复
聚合酶链反应
秀丽隐杆线虫
黑腹果蝇
分子生物学
DNA
遗传学
计算生物学
基因
作者
Senyene E. Hunter,Dawoon Jung,Richard T. Di Giulio,Joel N. Meyer
出处
期刊:Methods
[Elsevier BV]
日期:2010-02-02
卷期号:51 (4): 444-451
被引量:156
标识
DOI:10.1016/j.ymeth.2010.01.033
摘要
The quantitative polymerase chain reaction (QPCR) assay allows measurement of DNA damage in the mitochondrial and nuclear genomes without isolation of mitochondria. It also permits measurement of relative mitochondrial genome copy number. Finally, it can be used for measurement of DNA repair in vivo when employed appropriately. In this manuscript we briefly review the methodology of the QPCR assay, discuss its strengths and limitations, address considerations for measurement of mitochondrial DNA repair, and describe methodological changes implemented in recent years. We present QPCR assay primers and reaction conditions for five species not previously described in a methods article: Caenorhabditis elegans, Fundulus heteroclitus, Danio rerio, Drosophila melanogaster, and adenovirus. Finally, we illustrate the use of the assay by measuring repair of ultraviolet C radiation-induced DNA damage in the nuclear but not mitochondrial genomes of a zebrafish cell culture.
科研通智能强力驱动
Strongly Powered by AbleSci AI