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首页> 外文期刊>Biochemical and Biophysical Research Communications >Sandwiched zinc-finger nucleases harboring a single-chain FokI dimer as a DNA-cleavage domain.
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Sandwiched zinc-finger nucleases harboring a single-chain FokI dimer as a DNA-cleavage domain.

机译:夹有锌指的核酸酶,具有单链FokI二聚体,可作为DNA切割域。

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摘要

Zinc-finger nucleases (ZFNs) are a powerful tool for manipulation of genomic DNA. Recently, we reported a new ZFN composed of one artificial zinc-finger protein (AZP) and a single-chain FokI dimer (scFokI) that refines ZFN technology. While AZP-scFokI cleaved DNA specifically around the AZP-target site, several nucleotide positions were cleaved due to the mobility of the scFokI domain. In the present study, we aimed to improve the DNA-cleavage specificity at the nucleotide level. To this end, we sandwiched a scFokI domain between two AZPs to reduce the mobility of the scFokI moiety when bound to DNA. We demonstrated that the AZP-sandwiched scFokI cleaved DNA at a single nucleotide position of a target plasmid, in which two AZP-binding sites were connected with a 6-bp spacer, with multiple turnovers. Further improvement of AZP-sandwiched scFokI will lead to development of ideal artificial meganucleases.
机译:锌指核酸酶(ZFN)是操纵基因组DNA的强大工具。最近,我们报道了一种由一种人工锌指蛋白(AZP)和一种单链FokI二聚体(scFokI)组成的新型ZFN,该ZFN技术完善了ZFN技术。尽管AZP-scFokI在AZP靶位点附近特异性切割了DNA,但由于scFokI域的移动性,几个核苷酸位置也被切割了。在本研究中,我们旨在提高核苷酸水平的DNA切割特异性。为此,我们将scFokI结构域夹在两个AZP之间,以减少与DNA结合时scFokI部分的迁移。我们证明了AZP夹心的scFokI在目标质粒的单个核苷酸位置切割了DNA,其中两个AZP结合位点与6 bp的间隔基连接,具有多个转换。 AZP夹心的scFokI的进一步改进将导致开发理想的人工大范围核酸酶。

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