Reifenberger Jeffrey G, Dorfman Kevin D, Cao Han
BioNano Genomics, 9640 Towne Centre Drive, Ste 100, San Diego, CA 92121, USA.
Analyst. 2015 Jul 21;140(14):4887-94. doi: 10.1039/c5an00343a. Epub 2015 May 20.
We present experimental data concerning potential topological events such as folds, internal backfolds, and/or knots within long molecules of double-stranded DNA when they are stretched by confinement in a nanochannel. Genomic DNA from E. coli was labeled near the 'GCTCTTC' sequence with a fluorescently labeled dUTP analog and stained with the DNA intercalator YOYO. Individual long molecules of DNA were then linearized and imaged using methods based on the NanoChannel Array technology (Irys® System) available from BioNano Genomics. Data were collected on 189 153 molecules of length greater than 50 kilobases. A custom code was developed to search for abnormal intensity spikes in the YOYO backbone profile along the length of individual molecules. By correlating the YOYO intensity spikes with the aligned barcode pattern to the reference, we were able to correlate the bright intensity regions of YOYO with abnormal stretching in the molecule, which suggests these events were either a knot or a region of internal backfolding within the DNA. We interpret the results of our experiments involving molecules exceeding 50 kilobases in the context of existing simulation data for relatively short DNA, typically several kilobases. The frequency of these events is lower than the predictions from simulations, while the size of the events is larger than simulation predictions and often exceeds the molecular weight of the simulated molecules. We also identified DNA molecules that exhibit large, single folds as they enter the nanochannels. Overall, topological events occur at a low frequency (∼7% of all molecules) and pose an easily surmountable obstacle for the practice of genome mapping in nanochannels.
我们展示了关于双链DNA长分子在纳米通道中受限制拉伸时可能出现的拓扑事件(如折叠、内部反向折叠和/或纽结)的实验数据。大肠杆菌的基因组DNA在“GCTCTTC”序列附近用荧光标记的dUTP类似物进行标记,并用DNA嵌入剂YOYO进行染色。然后,使用来自BioNano Genomics的基于纳米通道阵列技术(Irys®系统)的方法,将单个DNA长分子线性化并成像。收集了189153个长度大于50千碱基的分子的数据。开发了一个自定义代码,以搜索沿单个分子长度的YOYO主链轮廓中的异常强度峰值。通过将YOYO强度峰值与对齐的条形码模式与参考进行关联,我们能够将YOYO的明亮强度区域与分子中的异常拉伸相关联,这表明这些事件要么是一个纽结,要么是DNA内部的反向折叠区域。我们在相对较短的DNA(通常为几千碱基)的现有模拟数据的背景下,解释了我们涉及超过50千碱基分子的实验结果。这些事件的频率低于模拟预测,而事件的大小大于模拟预测,并且常常超过模拟分子的分子量。我们还鉴定出在进入纳米通道时呈现大的单折叠的DNA分子。总体而言,拓扑事件发生频率较低(约占所有分子的7%),并且对纳米通道中的基因组图谱绘制实践构成了一个易于克服的障碍。