Random shearing as an alternative to digestion for mitochondrial DNA processing in droplet digital PCR

被引:4
|
作者
Vitomirov, Andrej [1 ]
Ramirez-Gaona, Miguel [2 ]
Mehta, Sanjay R. [1 ,3 ]
Perez-Santiago, Josue [1 ]
机构
[1] Univ Calif San Diego, 9500 Gilman Dr,Stein Res Bldg Room 324, La Jolla, CA 92093 USA
[2] Univ Alberta, 116 St & 85 Ave, Edmonton, AB T6G 2R3, Canada
[3] Vet Adm San Diego Healthcare Syst, 3350 La Jolla Village Dr, San Diego, CA 92161 USA
基金
美国国家卫生研究院;
关键词
Droplet digital PCR; Mitochondrial DNA; Mitochondrial common deletion; Sonication; QIAshredder; DYSFUNCTION; SYSTEM;
D O I
10.1016/j.mito.2016.11.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Droplet digital PCR (ddPCR) is a quantitative assay that requires DNA fragmentation to maximize reaction efficiency. Here, we measured the proportion of mitochondrial DNA (mtDNA) carrying the "common deletion," a rare event, to compare quantification sensitivities between alternative DNA fragmentation methods (sonication and QIAshredder spin columns) against enzymatic digestion (traditionally used). QIAshredder showed the highest sensitivity when compared to sonication, followed by digestion. Also, both sonication and QIAshredder fragmentation had shorter processing times than enzymatic digestion; therefore, QIAshredder fragmentation and sonication are alternative DNA processing methods that maximize ddPCR quantification for the detection of rare events. (C) 2016 Published by Elsevier B.V. on behalf of Mitochondria Research Society.
引用
收藏
页码:16 / 18
页数:3
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