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Efficient generation of knock out mice by the CRISPR/Cas9 system with two guide RNAs

机译:具有两个引导RNA的CRISPR / Cas9系统可高效产生敲除小鼠

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摘要

The CRISPR/Cas9 system is a powerful genome editing tool for generating knockout mice. To generate mutant mice, single guide RNA (sgRNA) for tyrosinase was transcribed in vitro with template Oligo DNA and a mixture of either one or two sgRNAs and Cas9 mRNA were microinjected into the fertilized eggs of C57BL/6J( black hairs and eyes). To determine whether tyrosinase gene is successfully knocked out, their phenotype( black hairs/eyes or albino) was observed.  In this study, to investigate whether knockout efficiency can be increased by microinjection of two sgRNAs, either one or two sgRNAs were microinjected. Results indicated that when one sgRNA was microinjected, albino mice were obtained at relatively low efficiency (3/16, 19% or 13/23, 65%); however, the efficiency was increased by microinjecting two sgRNAs (24/26 92.9%). In conclusion, we demonstrate here that knockout mice at F0 can be obtained by microinjection of two sgRNA and Cas9 mRNA at high efficiency.
机译:CRISPR / Cas9系统是用于生成基因敲除小鼠的强大基因组编辑工具。为了产生突变小鼠,将酪氨酸酶的单向导RNA(sgRNA)与模板寡核苷酸DNA体外转录,并将一种或两种sgRNA和Cas9 mRNA的混合物显微注射到C57BL / 6J受精卵(黑发和眼睛)中。为了确定是否成功敲除酪氨酸酶基因,观察了它们的表型(黑发/眼睛或白化病)。在这项研究中,为了研究是否可以通过显微注射两种sgRNA来提高敲除效率,显微注射一种或两种sgRNA。结果表明,当微量注射一种sgRNA时,获得的白化病小鼠效率相对较低(3 / 16、19%或13 / 23、65%);然而,通过微量注射两种sgRNA,效率得以提高(24/26 92.9%)。总而言之,我们在这里证明可以通过高效注射两个sgRNA和Cas9 mRNA来获得F0的敲除小鼠。

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