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A序列结构中的协同性以及复合TnAn模块的弯曲特性

Cooperativity in A-tract structure and bending properties of composite TnAn blocks.

作者信息

Haran T E, Crothers D M

机构信息

Department of Chemistry, Yale University, New Haven, Connecticut 06511.

出版信息

Biochemistry. 1989 Apr 4;28(7):2763-7. doi: 10.1021/bi00433a003.

Abstract

The existence of intrinsically curved DNA molecules incorporating short runs of adenines is undisputed, but none of the current models can explain the entire experimental data set. Recently, Burkhoff and Tullius [Burkhoff, A. M., & Tullius, T. D. (1988) Nature 331, 455-457] offered an explanation for Hagerman's observations on A4T4N2 vs T4A4N2 polymers [Hagerman, P. J. (1986) Nature 321, 449-450], which showed that A4T4N2 multimers migrate anomalously slowly on polyacrylamide gels and T4A4N2 multimers migrate normally. In A4T4N2 multimers Burkhoff and Tullius observe a hydroxy-radical cutting pattern associated with bent DNA and a B-like cutting pattern in T4A4N2. They attribute this difference in cutting pattern to a clash in the TA step of T4A4N2 and suggest that TA4N5 might already adopt an unbent B-DNA conformation [Tullius T. D., & Burkhoff, A. M. (1988) in Structure and Expression. Vol. 3: DNA Bending and Curvature (Olson, W. K., Sarma, M. H., Sarma, R. H., & Sundaralingam, M., Eds.) pp 77-85, Adenine Press, Guilderland, NY]. We show that the conformation adopted by TnAn blocks is similar to that of AnTn blocks. Two A-tract structures of opposite polarity coexist in both blocks. Moreover, we demonstrate a cooperative buildup of a T-tract structure adjacent to an A-tract structure that cannot be predicted by any of the current models. We conclude that AA steps do not assume the same conformation in long tracts of A's as in isolated AA steps. Therefore, the assumption of nearest-neighbor models, that global curvature is an additive phenomenon of local effects, is invalid.

摘要

包含短腺嘌呤序列的内在弯曲DNA分子的存在是无可争议的,但目前的模型都无法解释整个实验数据集。最近,伯克霍夫和图利乌斯[伯克霍夫,A. M.,& 图利乌斯,T. D.(1988年)《自然》331卷,455 - 457页]对哈格曼关于A4T4N2与T4A4N2聚合物的观察结果给出了解释[哈格曼,P. J.(1986年)《自然》321卷,449 - 450页],该观察结果表明A4T4N2多聚体在聚丙烯酰胺凝胶上迁移异常缓慢,而T4A4N2多聚体迁移正常。在A4T4N2多聚体中,伯克霍夫和图利乌斯观察到与弯曲DNA相关的羟基自由基切割模式以及T4A4N2中的B样切割模式。他们将这种切割模式的差异归因于T4A4N2中TA步的冲突,并表明TA4N5可能已经采用了未弯曲的B - DNA构象[图利乌斯,T. D.,& 伯克霍夫,A. M.(1988年)载于《结构与表达》。第3卷:DNA弯曲与曲率(奥尔森,W. K.,萨尔马,M. H.,萨尔马,R. H.,& 桑达拉林加姆,M. 编)第77 - 85页,腺嘌呤出版社,纽约州圭尔德兰]。我们表明TnAn片段采用的构象与AnTn片段相似。在两个片段中都共存着两种相反极性的A - 序列结构。此外,我们证明了与A - 序列结构相邻的T - 序列结构的协同形成,这是目前任何模型都无法预测的。我们得出结论,AA步在长腺嘌呤序列中所呈现的构象与孤立的AA步不同。因此,最近邻模型中关于全局曲率是局部效应的累加现象这一假设是无效的。

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