Giolai Michael, Paajanen Pirita, Verweij Walter, Percival-Alwyn Lawrence, Baker David, Witek Kamil, Jupe Florian, Bryan Glenn, Hein Ingo, Jones Jonathan D G, Clark Matthew D
Earlham Institute (EI), Norwich Research Park, Norwich, UK.
The Sainsbury Laboratory, Norwich Research Park, Norwich, UK.
Biotechniques. 2016 Dec 1;61(6):315-322. doi: 10.2144/000114484.
Targeted capture provides an efficient and sensitive means for sequencing specific genomic regions in a high-throughput manner. To date, this method has mostly been used to capture exons from the genome (the exome) using short insert libraries and short-read sequencing technology, enabling the identification of genetic variants or new members of large gene families. Sequencing larger molecules results in the capture of whole genes, including intronic and intergenic sequences that are typically more polymorphic and allow the resolution of the gene structure of homologous genes, which are often clustered together on the chromosome. Here, we describe an improved method for the capture and single-molecule sequencing of DNA molecules as large as 7 kb by means of size selection and optimized PCR conditions. Our approach can be used to capture, sequence, and distinguish between similar members of the NB-LRR gene family-key genes in plant immune systems.
靶向捕获为以高通量方式对特定基因组区域进行测序提供了一种高效且灵敏的方法。迄今为止,该方法主要用于使用短插入文库和短读长测序技术从基因组中捕获外显子(外显子组),从而能够鉴定遗传变异或大型基因家族的新成员。对更大的分子进行测序可实现对整个基因的捕获,包括通常具有更多多态性的内含子和基因间序列,并能够解析同源基因的基因结构,这些同源基因通常在染色体上聚集在一起。在此,我们描述了一种通过大小选择和优化的PCR条件对长达7 kb的DNA分子进行捕获和单分子测序的改进方法。我们的方法可用于捕获、测序并区分植物免疫系统中的关键基因——NB-LRR基因家族的相似成员。