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Evaluating the probability of CRISPR‐based gene drive contaminating another species

机译:评估污染其他物种的基于CRISPR的基因驱动的概率

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摘要

The probability D that a given clustered regularly interspaced short palindromic repeats (CRISPR)‐based gene drive element contaminates another, nontarget species can be estimated by the following Drive Risk Assessment Quantitative Estimate (DRAQUE) Equation: with  = probability of hybridization between the target species and a nontarget species;  = probability of horizontal transfer of a piece of DNA containing the gene drive cassette from the target species to a nontarget species (with no hybridization);  = probability that the and guide RNA genes are expressed;  = probability that the CRISPR‐guide RNA recognizes and cuts at a DNA site in the new host;  = probability that the gene drive cassette inserts at the cut site;  = probability that the immune system does not reject ‐expressing cells;  = probability of invasion of the drive within the population. We discuss and estimate each of the seven parameters of the equation, with particular emphasis on possible transfers within insects, and between rodents and humans. We conclude from current data that the probability of a gene drive cassette to contaminate another species is not insignificant. We propose strategies to reduce this risk and call for more work on estimating all the parameters of the formula.
机译:给定聚集的概率D定期间隙的短语重复(CRISPR)基因驱动元件另一个,可以通过以下驱动风险评估定量估计(Draque)等式来估算Nontarget物种:=靶物种之间杂交的概率和不确定的物种; =将含有基因驱动盒的DNA水平转移的概率从靶物种到Nontarget物种(没有杂交); =表达和引导RNA基因的概率; = CRISPR导向RNA在新宿主中的DNA位点识别和切割的概率; =基因驱动盒插入切割部位的概率; =免疫系统不抑制细胞的概率; =侵入人口中的驱动器的概率。我们讨论和估计等式的七个参数中的每一个,特别强调昆虫中可能的转移,以及啮齿动物和人类之间的可能转移。我们从目前的数据得出结论,即基因驱动盒污染另一种物种的概率并不微不足道。我们提出了减少这种风险的策略,并呼吁估计公式的所有参数的更多工作。

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