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相控(dA)5序列的热力学与预熔构象变化

Thermodynamics and premelting conformational changes of phased (dA)5 tracts.

作者信息

Chan S S, Breslauer K J, Austin R H, Hogan M E

机构信息

Department of Chemistry, Rutgers University, Piscataway, New Jersey 08855-0939.

出版信息

Biochemistry. 1993 Nov 9;32(44):11776-84. doi: 10.1021/bi00095a005.

Abstract

Using synthetic 45 bp long DNAs of known sequences, we have studied (i) the unusual structure that the phased A-tracts have at temperatures below 37 degrees C, (ii) the thermodynamics of the loss of that aberrant structure well below the duplex melting temperature, and (iii) the conformational changes that occur with temperature. Using temperature-dependent circular dichroism, we detect a low-temperature structural transition in a 45-mer duplex with four segments of phased (dA)5 tracks separated by five segments of five randomized G-C pairs, but none in the corresponding isomeric random sequence 45-mer duplex. Differential scanning calorimetry measurements reveal the enthalpy of this preglobal melting transition to be 3.5 kcal/mol.AT pair or 4.4 kcal/mol.AA step. The integrated enthalpy change for this helix-to-helix intramolecular event only is about 16% of the global duplex-to-single-strands melting enthalpy and is relatively broad compared to the global melting event (about 30 vs 15 degrees C for the full width at half maxima). Electric birefringence decay measurements show that the phased 45 bp duplex has a rotational time constant of 100 ns at 5 degrees C which increases to 220 ns above 40 degrees C. Simple modeling of the dynamics within the junction model for bending yields that the bend per A-tract is 42 degrees at 5 degrees C, decreasing to 0 degrees above 40 degrees C. We suggest that this sequence-dependent structure which "melts" at physiological temperatures may be relevant to DNA topology and function.

摘要

我们使用已知序列的合成45个碱基对长的DNA,研究了:(i)在低于37摄氏度的温度下,相间A序列所具有的异常结构;(ii)在远低于双链解链温度时该异常结构丧失的热力学性质;以及(iii)随温度发生的构象变化。利用温度依赖的圆二色性,我们在一个45聚体双链体中检测到低温结构转变,该双链体有四段由五段随机G-C对隔开的相间(dA)5序列,但在相应的异构随机序列45聚体双链体中未检测到。差示扫描量热法测量显示,这种全局预解链转变的焓为3.5千卡/摩尔·AT对或4.4千卡/摩尔·AA步。仅该螺旋间分子内事件的积分焓变约为双链体到单链全局解链焓的16%,并且与全局解链事件相比相对较宽(半峰全宽约为30摄氏度对15摄氏度)。电双折射衰减测量表明,相间的45个碱基对双链体在5摄氏度时的旋转时间常数为100纳秒,在40摄氏度以上增加到220纳秒。在弯曲的连接点模型内对动力学进行简单建模得出,在5摄氏度时每个A序列的弯曲角度为42度,在40摄氏度以上降至0度。我们认为,这种在生理温度下“解链”的序列依赖性结构可能与DNA拓扑结构和功能相关。

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