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A novel four zinc-finger protein targeted against p190BcrAbl fusion oncogene cDNA: utilisation of zinc-finger recognition codes

机译:针对p190BcrAbl融合癌基因cDNA的新型四个锌指蛋白:利用锌指识别码

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A three zinc-finger protein that binds specifically to the cDNA representing the unique fusion gene BcrAbl, associated with acute lymphoblastic leukaemia, has previously been characterised. At this breakpoint, a sequence homology of 8/9 bp exists between the BcrAbl (fusion) and c-Abl (parental) target sequences. We show that the three zinc-finger protein discriminates poorly between the fusion (BcrAbl) and parental (Abl) sequence (Kds of 42.8 and 65.1 nM, respectively). In order to improve the discriminatory properties of this protein, and to demonstrate the utility of current zinc-finger databases, we have added a fourth zinc-finger to the original three zinc-finger protein. This fourth finger recognises a 3 bp subsite derived from the Bcr portion of the breakpoint and is not present in c-Abl. This novel four finger protein, which now recognises a 12 bp sequence, demonstrates improved specific binding to BcrAbl (Kd = 17 nM). More significantly we have shown that there is now enhanced discrimination between BcrAbl and Abl sequences by the four finger protein than the original three finger protein.
机译:先前已经鉴定了三种锌指蛋白,其与代表独特融合基因BcrAbl的cDNA特异性结合,与急性淋巴细胞白血病有关。在此断点处,BcrAbl(融合)和c-Abl(亲本)靶序列之间存在8/9 bp的序列同源性。我们表明,这三个锌指蛋白在融合序列(BcrAbl)和亲本序列(Abl)之间的区分差(分别为42.8和65.1 nM的K d)。为了改善该蛋白的区分特性,并证明当前锌指数据库的实用性,我们在原始的三个锌指蛋白中添加了第四个锌指。该第四根手指识别出源自断点的Bcr部分的3 bp亚位点,并不存在于c-Abl中。这种新颖的四指蛋白现在可以识别12 bp的序列,证明与BcrAbl的特异性结合得以改善(K d = 17 nM)。更重要的是,我们已经表明,与原始的三指蛋白相比,现在四指蛋白在BcrAbl和Abl序列之间的区别得到增强。

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