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First progeria monkey model generated using base editor

机译:使用基本编辑器生成的第一个Progeria Monkey模型

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In this issue, Wang et al. report on the generation of a nonhumanprimate model of Hutchinson-Gilford progeria syndrome(HGPS) using a base editor. Base editing is anemerging novel genome editing technique for modifying asingle base pair at specific sites in the genome. Base editors(BEs) have two principal components, a catalytically inactiveor single strand cleaving Cas-variant, which binds to theguide RNA and a nucleobase deaminase domain to convertspecific base pairs at the target loci (Komor et al., 2016;Nishida et al., 2016; Gaudelli et al., 2017). Cytosine baseeditor (CBE) and adenine base editor (ABE) are two baseeditors,which convert Cytosine-Guanine (C-G) to ThymineAdenine(T-A) and A-T to G-C, respectively. Likewise, RNAbase editor (RBE) was created by fusing nucleobasedeaminases with the Cas13 protein, which allows for a basesubstitution of A to inosine (I) or C to uracil (U) in the targetedRNA (Cox et al., 2017). Recently, a dual base editor wasdeveloped that can catalyze both cytosine and adenine baseconversions at the same time, broadening base editingcapability (Zhang et al., 2020).
机译:在这个问题中,Wang等人。使用基本编辑器兼出Hutchinson-Gilford Progeria综合征(HGPS)非体力利用模型的报告。基础编辑是一种用于在基因组中特定位点的修饰asingle碱基对的一种新型基因组编辑技术。基础编辑器(BES)具有两个主要成分,一种催化惰性单链切割CAS变体,其与导点RNA和核碱基脱氨酶结构域结合到目标基因座的转化特异性碱对(Komor等,2016; Nishida等人。 ,2016; Gaudelli等人。,2017)。胞嘧啶碱基管(CBE)和腺嘌呤基础编辑器(ABE)是两种基础对立剂,将胞嘧啶 - 鸟嘌呤(C-G)转化为胸腺烯(T-A)和A-T至G-C。同样地,通过用CAS13蛋白熔化核咔哒胺酶来创建rnabase编辑器(Rbe),这允许在TargetEdRNA中允许A inosine(I)或C至Uracil(U)的基础溶解物(Cox等,2017)。最近,双基础编辑器是培养的,可以同时催化胞嘧啶和腺嘌呤基座Versions,拓宽基础编辑性(Zhang等,2020)。

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