Price M A, Tullius T D
Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218.
Biochemistry. 1993 Jan 12;32(1):127-36. doi: 10.1021/bi00052a018.
We present a new model to explain the bending and local structural properties of TnAn sequences in DNA. Current models suggest that an adenine tract has the same unusual structure when found in a TnAn sequence as it has when surrounded by mixed-sequence B-DNA. On the basis of hydroxyl radical cleavage patterns of several TnAn sequences, we instead propose that the T2A2 or T3A3 core of such sequences is B-DNA-like but that adenines and thymines outside of this core, if sufficient in number, can form the unusual structure adopted by adenine tracts surrounded by mixed sequence DNA. We pursued further the structure of T7A7N7, a molecule which exhibits reduced electrophoretic mobility on native polyacrylamide gels and is therefore presumed to be bent. We attempted to mimic the structure of T7A7N7 that was predicted by our model by designing two new sequences, one in which the T3A3 core of T7A7N7 is substituted by six nucleotides of mixed sequence (N6) and the other in which the T2A2 core is replaced by N4. Hydroxyl radical cleavage patterns of all three molecules are nearly indistinguishable. All three molecules run anomalously slowly on a native polyacrylamide gel, with the mobility of T4N6A4N7 > T7A7N7 approximately T5N4A5N7. Analysis of the hydroxyl radical cutting pattern of T7A7N7 by Fourier transformation reveals the occurrence of an unusual structure at intervals of approximately 10 bp, a periodicity which is not evident in the sequence of the DNA.
我们提出了一个新模型来解释DNA中TnAn序列的弯曲和局部结构特性。目前的模型表明,腺嘌呤序列在TnAn序列中时具有与在混合序列B-DNA中时相同的异常结构。基于几个TnAn序列的羟基自由基切割模式,我们反而提出,此类序列的T2A2或T3A3核心类似B-DNA,但该核心之外的腺嘌呤和胸腺嘧啶如果数量足够,可形成被混合序列DNA包围的腺嘌呤序列所采用的异常结构。我们进一步研究了T7A7N7的结构,该分子在天然聚丙烯酰胺凝胶上表现出降低的电泳迁移率,因此被推测是弯曲的。我们试图通过设计两个新序列来模拟我们模型预测的T7A7N7的结构,一个新序列中T7A7N7的T3A3核心被六个混合序列核苷酸(N6)取代,另一个新序列中T2A2核心被N4取代。所有三个分子的羟基自由基切割模式几乎无法区分。所有三个分子在天然聚丙烯酰胺凝胶上的迁移异常缓慢,迁移率顺序为T4N6A4N7 > T7A7N7 ≈ T5N(4)A5N7。通过傅里叶变换对T7A7N7的羟基自由基切割模式进行分析,发现每隔约10 bp会出现一种异常结构,这种周期性在DNA序列中并不明显。