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Subculturing cells have no effect on CRISPR/Cas9‐mediated cleavage of UL30 gene in pseudorabies virus

机译:传代细胞对CRISPR / Cas9介导的伪狂犬病病毒UL30基因切割没有影响

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摘要

CRISPR/Cas9‐mediated genome editing can inhibit virus infection by targeting the conserved regions of the viral genomic DNA. Unexpectedly, we found previously that pseudorabies virus (PRV) could escape from CRISPR/Cas9‐mediated inhibition. In order to elucidate whether the escape of PRV from Cas9‐mediated inhibition was due to cell deficiencies, such as genetic instability of sgRNA or Cas9 protein, the positive cells were passaged ten times, and PRV infection in the sgRNA‐expressing cells was evaluated in the present study. The results showed that subculturing cells has no effect on Cas9‐mediated cleavage of PRV. Different passages of PX459‐PRV cells can stably express sgRNA to facilitate Cas9/sgRNA cleavage on the UL30 gene of PRV, resulting in a pronounced inhibition of PRV infection. Studies to elucidate the mechanism of style="fixed-case">PRV escape are currently in progress.
机译:CRISPR / Cas9介导的基因组编辑可通过靶向病毒基因组DNA的保守区域来抑制病毒感染。出乎意料的是,我们先前发现伪狂犬病病毒(PRV)可能会从CRISPR / Cas9介导的抑制作用中逃脱。为了阐明PRV是否从Cas9介导的抑制中逃逸是由于细胞缺陷引起的,例如sgRNA或Cas9蛋白的遗传不稳定性,将阳性细胞传代10次,并在表达sgRNA的细胞中评估PRV感染。本研究。结果表明,传代培养细胞对Cas9介导的PRV裂解没有影响。 PX459-PRV细胞的不同传代可以稳定表达sgRNA,以促进Cas9 / sgRNA在PRV的UL30基因上的裂解,从而显着抑制PRV感染。阐明 style =“ fixed-case”> PRV 逃逸机制的研究正在进行中。

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