Evrogen JSC, Moscow, Russia.
Biotechniques. 2010 Jun;48(6):455-9. doi: 10.2144/000113422.
An application of duplex-specific nuclease (DSN) normalization technology to whole-genome shotgun sequencing of genomes with a large proportion of repetitive DNA is described. The method uses a thermostable DSN from the Kamchatka crab that specifically hydrolyzes dsDNA. In model experiments on human genomic DNA, we demonstrated that DSN normalization of double-stranded DNA formed during C0t analysis is effective against abundant repetitive sequences with high sequence identity, while retaining highly divergent repeats and coding regions at base-line levels. Thus, DSN normalization applied to C0t analysis can be used to eliminate evolutionarily young repetitive elements from genomic DNA before sequencing, and should prove invaluable in studies of large eukaryotic genomes, such as those of higher plants.
描述了一种将双链特异性核酸酶(DSN)归一化技术应用于具有大量重复 DNA 比例的全基因组鸟枪法测序的方法。该方法使用来自堪察加蟹的耐热 DSN,该酶特异性水解 dsDNA。在人类基因组 DNA 的模型实验中,我们证明了 C0t 分析过程中形成的双链 DNA 的 DSN 归一化对具有高度序列同一性的丰富重复序列是有效的,同时保留了高度分化的重复序列和编码区的基线水平。因此,在测序前,应用于 C0t 分析的 DSN 归一化可以用于从基因组 DNA 中消除进化年轻的重复元件,并且应该在研究大型真核生物基因组(如高等植物基因组)方面非常有价值。