Møller Henrik Devitt
Department of Biology, Faculty of Science, University of Copenhagen, Copenhagen, Denmark.
Department of Biology, Institute of Biochemistry, ETH Zurich, Switzerland.
Methods Mol Biol. 2020;2119:165-181. doi: 10.1007/978-1-0716-0323-9_15.
Chromosome-derived extrachromosomal circular DNA elements (eccDNAs) are detected in all eukaryotes examined so far. Here I describe the Circle-Seq protocol, applicable for physical enrichment of eccDNAs of a broad size range, combined with sequence confirmation of circular structures.Briefly, by concise alkaline treatment and gentle gravity flow-through an ion-exchange column, eccDNAs are enriched in the eluate fraction. EccDNAs are enzymatically isolated by extensive Plasmid-Safe DNase digestion of linear chromosomes and further enriched by φ29 rolling circle amplification. By means of high throughput sequencing of amplified eccDNA and custom eccDNA mapping software, around ten-thousand unique eccDNA types could be detected at nucleotide resolution in a million human muscle nuclei by this method.
迄今为止,在所有已检测的真核生物中均发现了源自染色体的染色体外环状DNA元件(eccDNA)。在此,我描述了Circle-Seq方案,该方案适用于广泛大小范围的eccDNA的物理富集,并结合环状结构的序列确认。简而言之,通过简洁的碱性处理和离子交换柱的轻柔重力流通,eccDNA在洗脱液部分得到富集。通过对线性染色体进行广泛的质粒安全DNA酶消化,酶法分离eccDNA,并通过φ29滚环扩增进一步富集。通过对扩增的eccDNA进行高通量测序和定制的eccDNA图谱绘制软件,用这种方法在一百万个人类肌肉细胞核中可以在核苷酸分辨率下检测到大约一万种独特的eccDNA类型。