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通过下调非增殖性HeLa细胞中脱氧鸟苷激酶的表达来消耗线粒体DNA。

Depletion of mitochondrial DNA by down-regulation of deoxyguanosine kinase expression in non-proliferating HeLa cells.

作者信息

Franco Maribel, Johansson Magnus, Karlsson Anna

机构信息

Karolinska Institute, Mitochondrial Medicine Center, Stockholm, Sweden.

出版信息

Exp Cell Res. 2007 Jul 15;313(12):2687-94. doi: 10.1016/j.yexcr.2007.04.003. Epub 2007 Apr 6.

DOI:10.1016/j.yexcr.2007.04.003
PMID:17490647
Abstract

Purine deoxyribonucleotides required for mitochondrial DNA replication are either imported from the cytosol or derived from phosphorylation of deoxyadenosine or deoxyguanosine catalyzed by mitochondrial deoxyguanosine kinase (DGUOK). DGUOK deficiency has been linked to mitochondrial DNA depletion syndromes suggesting an important role for this enzyme in dNTP supply. We have generated HeLa cell lines with 20-30% decreased levels of DGUOK mRNA by the expression of small interfering RNAs directed towards the DGUOK mRNA. The cells with decreased expression of the enzyme showed similar levels of mtDNA as control cells when grown exponentially in culture. However, mtDNA levels rapidly decreased in the cells when cell cycle arrest was induced by serum starvation. DNA incorporation of 9-beta-d-arabino-furanosylguanine (araG) was lower in the cells with decreased deoxyguanosine kinase expression, but the total rate of araG phosphorylation was increased in the cells. The increase in araG phosphorylation was shown to be due to increased expression of deoxycytidine kinase. In summary, our findings show that DGUOK is required for mitochondrial DNA replication in resting cells and that small changes in expression of this enzyme may cause mitochondrial DNA depletion. Our data also suggest that alterations in the expression level of DGUOK may induce compensatory changes in the expression of other nucleoside kinases.

摘要

线粒体DNA复制所需的嘌呤脱氧核糖核苷酸要么从细胞质中导入,要么源自线粒体脱氧鸟苷激酶(DGUOK)催化的脱氧腺苷或脱氧鸟苷磷酸化。DGUOK缺乏与线粒体DNA耗竭综合征有关,表明该酶在dNTP供应中起重要作用。我们通过表达针对DGUOK mRNA的小干扰RNA,构建了DGUOK mRNA水平降低20 - 30%的HeLa细胞系。当在培养中指数生长时,该酶表达降低的细胞显示出与对照细胞相似的线粒体DNA水平。然而,当通过血清饥饿诱导细胞周期停滞时,这些细胞中的线粒体DNA水平迅速下降。脱氧鸟苷激酶表达降低的细胞中9-β-D-阿拉伯呋喃糖基鸟嘌呤(araG)的DNA掺入量较低,但细胞中araG磷酸化的总速率增加。结果表明,araG磷酸化增加是由于脱氧胞苷激酶表达增加所致。总之,我们的研究结果表明,DGUOK是静息细胞中线粒体DNA复制所必需的,该酶表达的微小变化可能导致线粒体DNA耗竭。我们的数据还表明,DGUOK表达水平的改变可能会诱导其他核苷激酶表达的代偿性变化。

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