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一个 HeLa 细胞系的基因组和转录组景观。

The genomic and transcriptomic landscape of a HeLa cell line.

机构信息

European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.

出版信息

G3 (Bethesda). 2013 Aug 7;3(8):1213-24. doi: 10.1534/g3.113.005777.

DOI:10.1534/g3.113.005777
PMID:23550136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3737162/
Abstract

HeLa is the most widely used model cell line for studying human cellular and molecular biology. To date, no genomic reference for this cell line has been released, and experiments have relied on the human reference genome. Effective design and interpretation of molecular genetic studies performed using HeLa cells require accurate genomic information. Here we present a detailed genomic and transcriptomic characterization of a HeLa cell line. We performed DNA and RNA sequencing of a HeLa Kyoto cell line and analyzed its mutational portfolio and gene expression profile. Segmentation of the genome according to copy number revealed a remarkably high level of aneuploidy and numerous large structural variants at unprecedented resolution. Some of the extensive genomic rearrangements are indicative of catastrophic chromosome shattering, known as chromothripsis. Our analysis of the HeLa gene expression profile revealed that several pathways, including cell cycle and DNA repair, exhibit significantly different expression patterns from those in normal human tissues. Our results provide the first detailed account of genomic variants in the HeLa genome, yielding insight into their impact on gene expression and cellular function as well as their origins. This study underscores the importance of accounting for the strikingly aberrant characteristics of HeLa cells when designing and interpreting experiments, and has implications for the use of HeLa as a model of human biology.

摘要

海拉细胞系是研究人类细胞和分子生物学最常用的模型细胞系。迄今为止,尚未发布该细胞系的基因组参考序列,实验依赖于人类参考基因组。使用海拉细胞进行的分子遗传学研究的有效设计和解释需要准确的基因组信息。在这里,我们对海拉细胞系进行了详细的基因组和转录组特征描述。我们对海拉京都细胞系进行了 DNA 和 RNA 测序,并分析了其突变组合和基因表达谱。根据拷贝数对基因组进行分割,揭示了极高水平的非整倍体和许多前所未有的分辨率的大型结构变体。一些广泛的基因组重排表明存在灾难性的染色体破碎,称为染色体重排。我们对海拉基因表达谱的分析表明,包括细胞周期和 DNA 修复在内的几个途径表现出与正常人类组织明显不同的表达模式。我们的研究结果提供了海拉基因组中基因组变异的第一个详细描述,深入了解了它们对基因表达和细胞功能的影响及其起源。这项研究强调了在设计和解释实验时考虑海拉细胞惊人异常特征的重要性,并对将海拉作为人类生物学模型的应用具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/450d56453b1c/1213f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/8bfa3804fb5d/1213f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/e2b68529ac46/1213f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/1240c4cce107/1213f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/450d56453b1c/1213f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/8bfa3804fb5d/1213f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/e2b68529ac46/1213f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/1240c4cce107/1213f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248f/3737162/450d56453b1c/1213f4.jpg

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