Marilley Monique, Milani Pascale, Rocca-Serra José
Laboratoire de régulation génique et fonctionnelle & microscopie champ proche (RGFCP), IFR 125, Faculté de Médecine, Réseau AFM, Université de la Méditerranée, 13385 Marseille cedex 5, France.
Biochimie. 2007 Apr;89(4):534-41. doi: 10.1016/j.biochi.2007.02.007. Epub 2007 Feb 23.
Local DNA melting is integral to fundamental processes such as replication or transcription. In vivo, these two processes do not occur on molecules free in solution but, instead, involve DNA molecules which are organized into DNA/proteins complexes. Atomic force microscopy imaging offers a possibility to look at individual molecules. It allowed us to follow the progress of local denaturation in liquid, but with the added constraints of DNA lying on a surface. We present a kinetic analysis of the mapping of the temperature-driven melting seen at a replication origin (Schizosaccharomyces pombe ars1). The results indicate an expected base composition dependency, but also a strong extremity effect. Noteworthy, a "structural" effect is clearly occurring - which is shown by the greater susceptibility of the strongly curved region present in the sequence to unwind. DNA melting, at this place, is seen to occur after an increase in the curvature amplitude and a simultaneous shift of the nucleotide sequence positioned at the apex. Because this may determine the position of the Replication Initiation (R.I.) site, the result suggests that eukaryotic replication origins, although described as possessing no consensus sequences, may well have their mechanics sustained by the properties of common structural features. Our analysis may, therefore, provide new information that will give genuine insights on how DNA molecules behave when organized into primosomes, replisomes, promoter initiation complexes, etc. and thus, be essential to better understanding the way genes function.
局部DNA解链对于诸如复制或转录等基本过程至关重要。在体内,这两个过程并非发生在溶液中游离的分子上,而是涉及组装成DNA/蛋白质复合物的DNA分子。原子力显微镜成像提供了观察单个分子的可能性。它使我们能够在液体中追踪局部变性的进程,但DNA位于表面这一情况增加了限制条件。我们对在复制起点(裂殖酵母ars1)观察到的温度驱动解链图谱进行了动力学分析。结果表明存在预期的碱基组成依赖性,同时也有强烈的末端效应。值得注意的是,明显出现了一种“结构”效应——序列中存在的强弯曲区域更易解链就表明了这一点。在此处,DNA解链是在曲率幅度增加以及位于顶端的核苷酸序列同时发生移位之后出现的。由于这可能决定复制起始(R.I.)位点的位置,该结果表明真核生物的复制起点虽然被描述为不具有共有序列,但很可能其机制由常见结构特征的性质所维持。因此,我们的分析可能会提供新的信息,从而真正深入了解DNA分子组装成引发体、复制体、启动子起始复合物等时的行为方式,进而对于更好地理解基因的功能发挥方式至关重要。