Investigating cellular heterogeneity at the single-cell level by the flexible and mobile extrachromosomal circular DNA

染色体外DNA 染色质 背景(考古学) DNA 计算生物学 增强子 细胞 生物 电池类型 基因组 遗传学 转录因子 基因 古生物学
作者
Jiajinlong Kang,Yulin Dai,Jinze Li,Huihui Fan,Zhongming Zhao
出处
期刊:Computational and structural biotechnology journal [Elsevier]
卷期号:21: 1115-1121 被引量:6
标识
DOI:10.1016/j.csbj.2023.01.025
摘要

Extrachromosomal circular DNA (eccDNA) is a special class of DNA derived from linear chromosomes. It coexists independently with linear chromosomes in the nucleus. eccDNA has been identified in multiple organisms, including Homo sapiens, and has been shown to play important roles relevant to tumor progression and drug resistance. To date, computational tools developed for eccDNA detection are only applicable to bulk tissue. Investigating eccDNA at the single-cell level using a computational approach will elucidate the heterogeneous and cell-type-specific landscape of eccDNA within cellular context. Here, we performed the first eccDNA analysis at the single-cell level using data generated by single-cell Assay for Transposase-Accessible Chromatin with sequencing (scATAC-seq) in adult and pediatric glioblastoma (GBM) samples. Glioblastoma multiforme (GBM) is an aggressive tumor of the central nervous system with a poor prognosis. Our analysis provides an overview of cellular origins, genomic distribution, as well as the differential regulations between linear and circular genome under disease- and cell-type-specific conditions across the open chromatin regions in GBM. We focused on some eccDNA elements that are potential mobile enhancers acting in a trans-regulation manner. In summary, this pilot study revealed novel eccDNA features in the cellular context of brain tumor, supporting the strong need for eccDNA investigation at the single-cell level.
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