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Cytotoxic Effects during Knock Out of Multiple Porcine Endogenous Retrovirus (PERV) Sequences in the Pig Genome by Zinc Finger Nucleases (ZFN)

机译:锌指基因核酸酶(ZFN)在猪基因组中敲除多个猪内源性逆转录病毒(pERV)序列时的细胞毒性效应

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摘要

Xenotransplantation has been proposed as a solution to the shortage of suitable human donors for transplantation and pigs are currently favoured as donor animals. However, xenotransplantation may be associated with the transmission of zoonotic microorganisms. Whereas most porcine microorganisms representing a risk for the human recipient may be eliminated by designated pathogen free breeding, multiple copies of porcine endogenous retroviruses (PERVs) are integrated in the genome of all pigs and cannot be eliminated this way. PERVs are released as infectious particles and infect human cells. The zinc finger nuclease (ZFN) technology allows knocking out specifically cellular genes, however it was not yet used to eliminate multiple integrated proviral sequences with a strong conservation in the target sequence. To reduce the risk of horizontal PERV transmission and to knock out as many as possible proviruses, for the first time the powerful tool of the ZFN technology was used. ZFN were designed to bind specifically to sequences conserved in all known replication-competent proviruses. Expression and transport of the ZFN into the nucleus was shown by Western blot analysis, co-localisation analysis, PLA and FRET. Survival of transfected cells was analysed using fluorescent ZFN and cell counting. After transfection a strong expression of the ZFN proteins and a co-localisation of the expressed ZFN proteins were shown. However, expression of the ZFN was found to be extremely toxic for the transfected cells. The induced cytotoxicity was likely due to the specific cutting of the high copy number of the PERV proviruses, which is also commonly observed when ZFN with low specificity cleave numerous off-target sites in a genome. This is the first attempt to knock out multiple, nearly identical, genes in a cellular genome using ZFN. The attempt failed, and other strategies should be used to prevent PERV transmission.
机译:已经提出异种移植作为解决用于移植的合适人类供体短缺的解决方案,并且目前猪被优选为供体动物。但是,异种移植可能与人畜共患病微生物的传播有关。尽管可以通过指定的无病原体繁殖消除代表人类受体风险的大多数猪微生物,但多头猪内源性逆转录病毒(PERV)已整合到所有猪的基因组中,无法通过这种方式消除。 PERV以感染性颗粒的形式释放并感染人类细胞。锌指核酸酶(ZFN)技术可以敲除特定的细胞基因,但是尚未用于消除目标序列中具有强烈保守性的多个整合前病毒序列。为了降低水平PERV传播的风险并消除尽可能多的原病毒,首次使用ZFN技术的强大工具。 ZFN被设计为与所有已知的具有复制能力的原病毒中保守的序列特异性结合。通过蛋白质印迹分析,共定位分析,PLA和FRET显示ZFN在核中的表达和转运。使用荧光ZFN和细胞计数分析转染细胞的存活。转染后,显示了ZFN蛋白的强表达和表达的ZFN蛋白的共定位。然而,发现ZFN的表达对转染的细胞具有极高的毒性。诱导的细胞毒性可能是由于PERV原病毒高拷贝数的特异切割所致,当低特异性ZFN切割基因组中许多脱靶位点时也通常观察到这种现象。这是使用ZFN敲除细胞基因组中多个几乎相同的基因的首次尝试。尝试失败,应使用其他策略来防止PERV传输。

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