首页> 美国卫生研究院文献>Biochemical Journal >Effect of a triplex-binding ligand on triple helix formation at a site within a natural DNA fragment.
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Effect of a triplex-binding ligand on triple helix formation at a site within a natural DNA fragment.

机译:三重结合的配体对天然DNA片段内某个位置的三重螺旋形成的影响。

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摘要

We have used DNase I footprinting to examine the effect of a triplex-binding ligand on the formation of parallel intermolecular DNA triple helices at a mixed sequence target site contained within a natural DNA fragment (tyrT). In the presence of 10 microM ligand (N-[2-(dimethylamino)ethyl]-2-(naphthyl)quinolin-4-ylamine), the binding of CTCTTTTTGCTT (12G) to the sequence GAGAAAAATGAA (generating a complex containing 8 x T x AT, 1 x G x TA and 3 x C+ x GC triplets) was enhanced 3-fold at pH 5.5. When the oligonucleotide CTCTTTTTTCTT (12T) was substituted for 12G (replacing G x TA with T x TA) there was a large reduction in affinity for the target sequence. However, this was stabilized by about 300-fold in the presence of the ligand, requiring a similar concentration to produce a footprint as 12G in the absence of the ligand. When the sequence of the target site was altered to GAGAAAAAAGAA, generating an uninterrupted run of purines [tyrT(46A)], the binding of 12T (generating a complex containing 9 x T x AT, and 3 x C+ x GC triplets) was enhanced 3-fold by 10 microM of the triplex-binding ligand. However, although the binding of 12G to this sequence generating a complex containing a G x AT triplet, was much weaker, this too was stabilized by about 30-fold by the ligand, requiring a similar concentration as the perfect matched oligonucleotide (12T) in the absence of the ligand. A secondary, less stable footprint was also observed in these fragments when using either 12T or 12G, which was evident only in the presence of the triplex-binding ligand. This site, which contained a number of triplet mismatches, appears to be realated to the formation of four or five central T x AT triplets. This reduction in the stringency of oligonucleotide binding by the triplex-binding ligand promotes the formation of complexes at non-targeted regions but may also have the potential for enabling recognition at sites that contain regions where there are no specific triplet matches.
机译:我们已使用DNase I足迹来检查三链体结合配体对天然DNA片段(tyrT)中包含的混合序列靶位点上平行分子间DNA三链螺旋形成的影响。在存在10 microM配体(N- [2-(二甲基氨基)乙基] -2-(萘基)喹啉-4-基胺)的情况下,CTCTTTTTGCTT(12G)与序列GAGAAAAATGAA的结合(生成的复合物包含8 x T x AT,1 x G x TA和3 x C + x GC三联体)在pH 5.5时提高了3倍。当寡核苷酸CTCTTTTTTCTT(12T)替换为12G(用T x TA替换G x TA)时,对靶序列的亲和力大大降低。但是,在存在配体的情况下,其稳定度约为300倍,需要类似的浓度才能在不存在配体的情况下产生与12G相同的足迹。当目标位点的序列更改为GAGAAAAAAGAA,生成不间断的嘌呤[tyrT(46A)]时,增强了12T的结合(生成包含9 x T x AT和3 x C + x GC三联体的复合物)。三倍结合配体的3倍乘10 microM。然而,尽管12G与该序列的结合产生了一个含G x AT三联体的复合物,虽然弱得多,但也被配体稳定了约30倍,需要与完全匹配的寡核苷酸(12T)相似的浓度。不存在配体。当使用12T或12G时,在这些片段中还观察到次要的,不稳定的足迹,这仅在存在三重结合配体的情况下才明显。该位点包含许多三联体错配,似乎可以实现四个或五个中央T x AT三联体的形成。通过三链体结合配体的寡核苷酸结合的严格性的这种降低促进了非靶向区域处复合物的形成,但是也可能具有使得能够在包含没有特定三链体匹配的区域的位点处进行识别的潜力。

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