Institute of Electronic Paper Displays, South China Academy for Advanced Optoelectronics, South China Normal University, Guangzhou Higher Education Mega Center, Guangzhou 510006, China.
Joint International Research Laboratory of Optical Information of the Chinese Ministry of Education, South China Normal University, Guangzhou Higher Education Mega Center, Guangzhou 510006, China.
Sci Rep. 2017 Jan 18;7:40745. doi: 10.1038/srep40745.
DNA fragmentation down to a precise fragment size is important for biomedical applications, disease determination, gene therapy and shotgun sequencing. In this work, a cheap, easy to operate and high efficiency DNA fragmentation method is demonstrated based on hydrodynamic shearing in a bubbling system. We expect that hydrodynamic forces generated during the bubbling process shear the DNA molecules, extending and breaking them at the points where shearing forces are larger than the strength of the phosphate backbone. Factors of applied pressure, bubbling time and temperature have been investigated. Genomic DNA could be fragmented down to controllable 1-10 Kbp fragment lengths with a yield of 75.30-91.60%. We demonstrate that the ends of the genomic DNAs generated from hydrodynamic shearing can be ligated by T4 ligase and the fragmented DNAs can be used as templates for polymerase chain reaction. Therefore, in the bubbling system, DNAs could be hydrodynamically sheared to achieve smaller pieces in dsDNAs available for further processes. It could potentially serve as a DNA sample pretreatment technique in the future.
DNA 碎片化到精确的片段大小对于生物医学应用、疾病确定、基因治疗和鸟枪法测序非常重要。在这项工作中,我们展示了一种基于冒泡系统中流体动力剪切的廉价、易于操作和高效的 DNA 碎片化方法。我们期望在冒泡过程中产生的流体动力在剪切力大于磷酸骨架强度的地方拉伸和断裂 DNA 分子。研究了施加压力、冒泡时间和温度等因素。基因组 DNA 可以被碎片化到可控的 1-10 Kbp 片段长度,产率为 75.30-91.60%。我们证明,从流体动力剪切产生的基因组 DNA 的末端可以通过 T4 连接酶连接,并且可以将碎片化的 DNA 用作聚合酶链反应的模板。因此,在冒泡系统中,可以通过流体动力剪切将 DNA 剪切为更小的片段,用于进一步的处理。它可能成为未来 DNA 样本预处理技术。