Meroni Alice, Mentegari Elisa, Crespan Emmanuele, Muzi-Falconi Marco, Lazzaro Federico, Podestà Alessandro
Dipartimento di Bioscienze, Università degli Studi di Milano, Milano, Italy.
DNA Enzymology and Molecular Virology, Institute of Molecular Genetics IGM-CNR, Pavia, Italy.
Biophys J. 2017 Oct 3;113(7):1373-1382. doi: 10.1016/j.bpj.2017.07.013.
Ribonucleotide incorporation is the most common error occurring during DNA replication. Cells have hence developed mechanisms to remove ribonucleotides from the genome and restore its integrity. Indeed, the persistence of ribonucleotides into DNA leads to severe consequences, such as genome instability and replication stress. Thus, it becomes important to understand the effects of ribonucleotides incorporation, starting from their impact on DNA structure and conformation. Here we present a systematic study of the effects of ribonucleotide incorporation into DNA molecules. We have developed, to our knowledge, a new method to efficiently synthesize long DNA molecules (hundreds of basepairs) containing ribonucleotides, which is based on a modified protocol for the polymerase chain reaction. By means of atomic force microscopy, we could therefore investigate the changes, upon ribonucleotide incorporation, of the structural and conformational properties of numerous DNA populations at the single-molecule level. Specifically, we characterized the scaling of the contour length with the number of basepairs and the scaling of the end-to-end distance with the curvilinear distance, the bending angle distribution, and the persistence length. Our results revealed that ribonucleotides affect DNA structure and conformation on scales that go well beyond the typical dimension of the single ribonucleotide. In particular, the presence of ribonucleotides induces a systematic shortening of the molecules, together with a decrease of the persistence length. Such structural changes are also likely to occur in vivo, where they could directly affect the downstream DNA transactions, as well as interfere with protein binding and recognition.
核糖核苷酸掺入是DNA复制过程中最常见的错误。因此,细胞已经发展出从基因组中去除核糖核苷酸并恢复其完整性的机制。事实上,核糖核苷酸在DNA中的持续存在会导致严重后果,如基因组不稳定和复制应激。因此,从核糖核苷酸对DNA结构和构象的影响开始,了解其掺入的影响变得很重要。在这里,我们对核糖核苷酸掺入DNA分子的影响进行了系统研究。据我们所知,我们开发了一种新方法,基于聚合酶链反应的改进方案,高效合成含有核糖核苷酸的长DNA分子(数百个碱基对)。通过原子力显微镜,我们能够在单分子水平上研究大量DNA群体在掺入核糖核苷酸后结构和构象性质的变化。具体来说,我们表征了轮廓长度与碱基对数目的标度关系、端到端距离与曲线距离的标度关系、弯曲角度分布以及持久长度。我们的结果表明,核糖核苷酸对DNA结构和构象的影响范围远远超出单个核糖核苷酸的典型尺寸。特别是,核糖核苷酸的存在会导致分子系统性缩短,同时持久长度降低。这种结构变化也可能在体内发生,在那里它们可能直接影响下游的DNA交易,以及干扰蛋白质的结合和识别。