线粒体DNA
生物
核DNA
遗传学
DNA测序
DNA
线粒体dna控制区
点突变
分子生物学
计算生物学
突变
基因
等位基因
单倍型
作者
Shilan Wu,Matthew J. Longley,Scott A. Lujan,Thomas A. Kunkel,William C. Copeland
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 427-441
标识
DOI:10.1007/978-1-0716-2922-2_28
摘要
Mitochondrial DNA (mtDNA) encodes components essential for cellular respiration. Low levels of point mutations and deletions accumulate in mtDNA during normal aging. However, improper maintenance of mtDNA results in mitochondrial diseases, stemming from progressive loss of mitochondrial function through the accelerated formation of deletions and mutations in mtDNA. To better understand the molecular mechanisms underlying the creation and propagation of mtDNA deletions, we developed the LostArc next-generation DNA sequencing pipeline to detect and quantify rare mtDNA species in small tissue samples. LostArc procedures are designed to minimize PCR amplification of mtDNA and instead achieve enrichment of mtDNA by selective destruction of nuclear DNA. This approach leads to cost-effective, high-depth sequencing of mtDNA with a sensitivity sufficient to identify one mtDNA deletion per million mtDNA circles. Here, we describe detailed protocols for isolation of genomic DNA from mouse tissues, enrichment of mtDNA through enzymatic destruction of linear nuclear DNA, and preparation of libraries for unbiased next-generation sequencing of mtDNA.
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