首页> 外文期刊>Nucleic Acids Research >Mb- and FnCpf1 nucleases are active in mammalian cells: activities and PAM preferences of four wild-type Cpf1 nucleases and of their altered PAM specificity variants
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Mb- and FnCpf1 nucleases are active in mammalian cells: activities and PAM preferences of four wild-type Cpf1 nucleases and of their altered PAM specificity variants

机译:MB-和FNCPF1核酸酶在哺乳动物细胞中活跃:四种野生型CPF1核酸酶的活性和PAM偏好以及其改变的PAM特异性变体

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摘要

Cpf1s, the RNA-guided nucleases of the class II clustered regularly interspaced short palindromic repeats system require a short motive called protospacer adjacent motif (PAM) to be present next to the targeted sequence for their activity. The TTTV PAM sequence of As- and LbCpf1 nucleases is relatively rare in the genome of higher eukaryotic organisms. Here, we show that two other Cpf1 nucleases, Fn- and MbCpf1, which have been reported to utilize a shorter, more frequently occurring PAM sequence (TTN) when tested in vitro, carry out efficient genome modification in mammalian cells. We found that all four Cpf1 nucleases showed similar activities and TTTV PAM preferences. Our approach also revealed that besides their activities their PAM preferences are also target dependent. To increase the number of the available targets for Fn- and MbCpf1 we generated their RVR and RR mutants with altered PAM specificity and compared them to the wild-type and analogous As- and LbCpf1 variants. The mutants gained new PAM specificities but retained their activity on targets with TTTV PAMs, redefining RR-Cpf1's PAM-specificities as TTYV/TCCV, respectively. These variants may become versatile substitutes for wild-type Cpf1s by providing an expanded range of targets for genome engineering applications.
机译:CPF1s,II类聚集的RNA引导核酸酶定期间隙的短语重复重复系统需要一个短暂的动机,称为Protospacer相邻的基序(PAM)旁边的靶向序列旁边的活性。在高等真菌生物体的基因组中,AS和LBCPF1核酸酶的TTTV PAM序列相对罕见。在这里,我们表明,在体外测试时,据报道,据报道,据报道的另外其他CPF1核酸酶,FN和MBCPF1在哺乳动物细胞中进行了有效的基因组改性。我们发现所有四个CPF1核酸次数都显示出类似的活动和TTTV PAM偏好。我们的方法还透露,除了他们的活动外,他们的PAM偏好也是依赖的目标。为了增加Fn-and MBCPF1的可用目标的数量,我们产生了具有改变的PAM特异性的RVR和RR突变体,并将其与野生型并类似于和LBCPF1变体进行比较。突变体获得了新的PAM特异性,但在具有TTTV PAM的目标上保留了它们的活动,分别将RR-CPF1的PAM特异性重新定义为TTYV / TCCV。通过为基因组工程应用的扩展目标提供扩展范围,这些变体可以对野生型CPF1S进行多功能替代品。

著录项

  • 来源
    《Nucleic Acids Research》 |2018年第19期|共14页
  • 作者单位

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

    Hungarian Acad Sci Inst Biochem Biol Res Ctr H-6726 Szeged Hungary;

    Hungarian Acad Sci Inst Enzymol Res Ctr Nat Sci H-1117 Budapest Hungary;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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