首页> 外文期刊>Nucleic Acids Research >A novel four zinc-finger protein targeted against p190(BcrAbl) fusion oncogene cDNA: utilisation of zinc-finger recognition codes.
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A novel four zinc-finger protein targeted against p190(BcrAbl) fusion oncogene cDNA: utilisation of zinc-finger recognition codes.

机译:一种新型的针对p190(BcrAbl)融合癌基因cDNA的四个锌指蛋白: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 BCR:Abl, associated with acute lymphoblastic leukaemia, has previously been characterised. At this breakpoint, a sequence homology of 8/9 bp exists between the BCR:Abl (fusion) and c-ABL: (parental) target sequences. We show that the three zinc-finger protein discriminates poorly between the fusion (BCR:Abl) and parental (ABL:) sequence (K:(d)s 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 (K:(d )= 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BCR:Abl的cDNA特异性结合,与急性淋巴细胞白血病有关。在此断点处,BCR:Abl(融合)和c-ABL :(亲本)靶序列之间存在8/9 bp的序列同源性。我们显示,这三个锌指蛋白在融合(BCR:Abl)和亲本(ABL :)序列(分别为42.8和65.1 nM的K:(d)s)之间难以区分。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。这第四个手指识别了一个来自BCR:断点部分的3 bp的亚位点,并且不存在于c-ABL中:这种新颖的四手指蛋白现在可以识别一个12 bp的序列,表明与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,四指蛋白在BcrAbl和ABL:序列之间的区别得到了增强。

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