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Expression levels of the human DNA repair protein metnase influence lentiviral genomic integration

机译:人类DNA修复蛋白metnase的表达水平影响慢病毒基因组整合

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We recently identified a Transposase domain protein called Metnase, which assists in repairing DNA double-strand breaks (DSB) via non-homologous end-joining (NHEJ), and is important for foreign DNA integration into a host cell genome. Since integration is essential for productive lentiviral infection we examined whether Metnase expression levels could have an influence on lentiviral genomic integration. Using cells stably transduced to either over- or under-express Metnase we determined that the expression level of Metnase did indeed correlate with live lentiviral integration. Changes in Metnase levels were accompanied by changes in the number of copies of integrated lentiviral cDNA. While Metnase levels affected lentiviral integration, it had no effect on the amount of either total cellular viral RNA, cDNA or 2-LTR circles. Therefore, Metnase enhances the integration of lentivirus DNA into the host cell genome.
机译:我们最近发现了一种称为Metnase的转座酶域蛋白,该蛋白可通过非同源末端连接(NHEJ)协助修复DNA双链断裂(DSB),对于将外源DNA整合入宿主细胞基因组非常重要。由于整合对于生产性慢病毒感染至关重要,因此我们检查了Metnase表达水平是否可能对慢病毒基因组整合产生影响。使用稳定转导过表达或表达不足的Metnase的细胞,我们确定Metnase的表达水平确实与慢病毒活体整合相关。 Metnase水平的变化伴随着整合的慢病毒cDNA拷贝数的变化。 Metnase水平影响慢病毒整合,但对总细胞病毒RNA,cDNA或2-LTR环的数量没有影响。因此,Metnase增强了慢病毒DNA整合入宿主细胞基因组的能力。

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