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Chimeric DNA:RNA Guide for High Accuracy Cas9 Genome Editing

机译:嵌合DNA:RNA Cas9基因组高精度编辑指南

摘要

A chimeric DNA:RNA guide for very high accuracy Cas9 genome editing employs nucleotide-type substitutions in nucleic acid-guided endonucleases for enhanced specificity. The CRISPR-Cas9 gene editing system is manipulated to generate chimeric DNA:RNA guide strands to minimize the off-target cleavage events of the S. pyogenes Cas9 endonuclease. A DNA:RNA chimeric guide strand is sufficient to guide Cas9 to a specified target sequence for indel formation and minimize off-target cleavage events due to the specificity conferred by DNA-DNA interactions. Use of chimeric mismatch-evading lowered-thermostability guides (“melt-guides”) demonstrate that nucleotide-type substitutions in the spacer can reduce cleavage of sequences mismatched by as few as a single base pair. The chimeric mismatch-evading lowered-thermostability guides replace most gRNA spacer positions with DNA bases to suppress mismatched targets under Cas9's catalytic threshold.
机译:用于非常高精度Cas9基因组编辑的嵌合DNA:RNA指南在核酸引导的核酸内切酶中采用核苷酸类型的取代来增强特异性。操纵CRISPR-Cas9基因编辑系统以生成嵌合DNA:RNA引导链,以最大程度地降低IS的脱靶切割事件。化脓 Cas9核酸内切酶。 DNA:RNA嵌合引导链足以将Cas9引导至指定的靶序列以形成插入缺失,并由于DNA-DNA相互作用赋予的特异性而使脱靶切割事件最小化。避免嵌合错配的降低热稳定性的指南(“熔解指南”)表明,间隔区中的核苷酸类型取代可以减少错配的序列的切割,少至单个碱基对。避免嵌合错配的降低热稳定性的指南用DNA碱基取代了大多数gRNA间隔子位置,以抑制Cas9催化阈值以下的错配靶标。

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