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多能干细胞细胞核中可逆的线粒体DNA积累。

Reversible mitochondrial DNA accumulation in nuclei of pluripotent stem cells.

作者信息

Schneider Joel S, Cheng Xin, Zhao Qingshi, Underbayev Chingiz, Gonzalez J Patrick, Raveche Elizabeth S, Fraidenraich Diego, Ivessa Andreas S

机构信息

1 Department of Cell Biology and Molecular Medicine, Rutgers Biomedical and Health Sciences , Newark, New Jersey.

出版信息

Stem Cells Dev. 2014 Nov 15;23(22):2712-9. doi: 10.1089/scd.2013.0630. Epub 2014 Aug 4.

Abstract

According to the endosymbiotic hypothesis, the precursor of mitochondria invaded the precursor of eukaryotic cells, a process that began roughly 2 billion years ago. Since then, the majority of the genetic material translocated from the mitochondria to the nucleus, where now almost all mitochondrial proteins are expressed. Only a tiny amount of DNA remained in the mitochondria, known as mitochondrial DNA (mtDNA). In this study, we report that the transfer of mtDNA fragments to the nucleus of pluripotent stem cells is still ongoing. We show by in situ hybridization and agarose DNA two-dimensional gel technique that induced pluripotent stem (iPS) cells contain high levels of mtDNA in the nucleus. We found that a large proportion of the accumulated mtDNA sequences appear to be extrachromosomal. Accumulation of mtDNA in the nucleus is present not only in the iPS cells, but also in embryonic stem (ES) cells. However upon differentiation, the level of mtDNA in the nuclei of iPS and ES cells is substantially reduced. This reversible accumulation of mtDNA in the nucleus supports the notion that the nuclear copy number of mtDNA sequences may provide a novel mechanism by which chromosomal DNA is dynamically regulated in pluripotent stem cells.

摘要

根据内共生假说,线粒体的前体侵入了真核细胞的前体,这一过程大约始于20亿年前。从那时起,大部分遗传物质从线粒体转移到细胞核,现在几乎所有的线粒体蛋白都是在细胞核中表达的。只有少量的DNA保留在线粒体中,称为线粒体DNA(mtDNA)。在本研究中,我们报告mtDNA片段向多能干细胞细胞核的转移仍在进行。我们通过原位杂交和琼脂糖DNA二维凝胶技术表明,诱导多能干细胞(iPS细胞)的细胞核中含有高水平的mtDNA。我们发现,大量积累的mtDNA序列似乎是染色体外的。mtDNA在细胞核中的积累不仅存在于iPS细胞中,也存在于胚胎干细胞(ES细胞)中。然而,在分化过程中,iPS细胞和ES细胞细胞核中的mtDNA水平会大幅降低。mtDNA在细胞核中的这种可逆积累支持了这样一种观点,即mtDNA序列的核拷贝数可能提供了一种新的机制,通过这种机制可以在多能干细胞中动态调节染色体DNA。

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