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CRISPR-CasΦ from huge phages is a hypercompact genome editor.
Science ( IF 44.7 ) Pub Date : 2020-07-17 , DOI: 10.1126/science.abb1400
Patrick Pausch 1, 2 , Basem Al-Shayeb 1, 3 , Ezra Bisom-Rapp 4 , Connor A Tsuchida 1, 5 , Zheng Li 6 , Brady F Cress 1, 2 , Gavin J Knott 1, 2, 7 , Steven E Jacobsen 6, 8 , Jillian F Banfield 1, 9 , Jennifer A Doudna 1, 2, 8, 10, 11, 12
Affiliation  

CRISPR-Cas systems are found widely in prokaryotes, where they provide adaptive immunity against virus infection and plasmid transformation. We describe a minimal functional CRISPR-Cas system, comprising a single ~70-kilodalton protein, CasΦ, and a CRISPR array, encoded exclusively in the genomes of huge bacteriophages. CasΦ uses a single active site for both CRISPR RNA (crRNA) processing and crRNA-guided DNA cutting to target foreign nucleic acids. This hypercompact system is active in vitro and in human and plant cells with expanded target recognition capabilities relative to other CRISPR-Cas proteins. Useful for genome editing and DNA detection but with a molecular weight half that of Cas9 and Cas12a genome-editing enzymes, CasΦ offers advantages for cellular delivery that expand the genome editing toolbox.



中文翻译:

来自巨大噬菌体的CRISPR-CasΦ是超紧凑基因组编辑器。

CRISPR-Cas系统广泛存在于原核生物中,它们可提供针对病毒感染和质粒转化的适应性免疫力。我们描述了一个最小功能的CRISPR-Cas系统,包括一个〜70千达尔顿蛋白,CasΦ和一个CRISPR阵列,仅在巨大噬菌体的基因组中编码。CasΦ使用单个活性位点进行CRISPR RNA(crRNA)加工和crRNA指导的DNA切割,以靶向外来核酸。该超紧凑型系统在体外以及在人和植物细胞中均具有活性,相对于其他CRISPR-Cas蛋白具有扩展的靶标识别能力。CasΦ可用于基因组编辑和DNA检测,但分子量仅为Cas9和Cas12a基因组编辑酶的一半,为细胞传递提供了优势,从而扩展了基因组编辑工具箱。

更新日期:2020-07-17
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