Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Nørre Alle 14, Copenhagen, 2200, Denmark.
Department of Micro- and Nanotechnology, Technical University of Denmark, Ørsteds Plads 345a, Kongens Lyngby, 2800, Denmark.
Sci Rep. 2017 Dec 20;7(1):17893. doi: 10.1038/s41598-017-18091-6.
Next-generation sequencing (NGS) has caused a revolution, yet left a gap: long-range genetic information from native, non-amplified DNA fragments is unavailable. It might be obtained by optical mapping of megabase-sized DNA molecules. Frequently only a specific genomic region is of interest, so here we introduce a method for selection and enrichment of megabase-sized DNA molecules intended for single-molecule optical mapping: DNA from a human cell line is digested by the NotI rare-cutting enzyme and size-selected by pulsed-field gel electrophoresis. For demonstration, more than 600 sub-megabase- to megabase-sized DNA molecules were recovered from the gel and analysed by denaturation-renaturation optical mapping. Size-selected molecules from the same gel were sequenced by NGS. The optically mapped molecules and the NGS reads showed enrichment from regions defined by NotI restriction sites. We demonstrate that the unannotated genome can be characterized in a locus-specific manner via molecules partially overlapping with the annotated genome. The method is a promising tool for investigation of structural variants in enriched human genomic regions for both research and diagnostic purposes. Our enrichment method could potentially work with other genomes or target specified regions by applying other genomic editing tools, such as the CRISPR/Cas9 system.
下一代测序(NGS)引发了一场革命,但仍存在一个空白:无法获得来自天然、未经扩增的 DNA 片段的长程遗传信息。这种信息可能通过对兆碱基大小的 DNA 分子进行光学作图获得。通常只有特定的基因组区域是人们感兴趣的,因此,我们在这里介绍一种用于选择和富集用于单分子光学作图的兆碱基大小 DNA 分子的方法:用人细胞系的 DNA 用稀切酶 NotI 进行酶切,然后通过脉冲场凝胶电泳进行大小选择。为了说明问题,我们从凝胶中回收了 600 多个亚兆碱基到兆碱基大小的 DNA 分子,并通过变性-复性光学作图进行分析。来自同一凝胶的大小选择分子通过 NGS 进行测序。光学作图分子和 NGS 读取结果显示,它们在 NotI 限制位点定义的区域中富集。我们证明,通过与注释基因组部分重叠的分子,可以以特定于基因座的方式对未注释的基因组进行特征描述。该方法是一种有前途的工具,可用于研究和诊断目的,在富含人类基因组区域中富集结构变体。通过应用其他基因组编辑工具,如 CRISPR/Cas9 系统,我们的富集方法有可能适用于其他基因组或特定的目标区域。