清脆的
生物
核糖核酸
基因组编辑
基因组
遗传学
引导RNA
Cas9
计算生物学
DNA
核酸内切酶
反式激活crRNA
基因
作者
Karthik Murugan,Arun S. Seetharam,Andrew Severin,Dipali G. Sashital
标识
DOI:10.1074/jbc.ra120.012933
摘要
cleavage assays to determine and compare the native cleavage specificities and activities of three different natural Cas12a orthologs (FnCas12a, LbCas12a, and AsCas12a). Surprisingly, we observed pervasive sequence-specific nicking of randomized target libraries, with strong nicking of DNA sequences containing up to four mismatches in the Cas12a-targeted DNA-RNA hybrid sequences. We also found that these nicking and cleavage activities depend on mismatch type and position and vary with Cas12a ortholog and CRISPR RNA sequence. Our analysis further revealed robust nonspecific nicking of dsDNA when Cas12a is activated by binding to a target DNA. Together, our findings reveal that Cas12a has multiple nicking activities against dsDNA substrates and that these activities vary among different Cas12a orthologs.
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