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Extraction of ultrashort DNA molecules from herbarium specimens

机译:从植物标本标本中提取超短DNA分子

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DNA extracted from herbarium specimens is highly fragmented; therefore, it is crucial to use extraction protocols that retrieve short DNA molecules. Improvements in extraction and DNA library preparation protocols for animal remains have allowed efficient retrieval of molecules shorter than 50 bp. Here, we applied these improvements to DNA extraction protocols for herbarium specimens and evaluated extraction performance by shotgun sequencing, which allows an accurate estimation of the distribution of DNA fragment lengths. Extraction with N-phenacylthiazolium bromide (PTB) buffer decreased median fragment length by 35% when compared with cetyl-trimethyl ammonium bromide (CTAB); modifying the binding conditions of DNA to silica allowed for an additional decrease of 10%. We did not observe a further decrease in length for single-stranded DNA (ssDNA) versus double-stranded DNA (dsDNA) library preparation methods. Our protocol enables the retrieval of ultrashort molecules from herbarium specimens, which will help to unlock the genetic information stored in herbaria.
机译:从植物标料标本中提取的DNA高度碎片;因此,使用检索短DNA分子的提取方案至关重要。用于动物的提取和DNA文库的改进仍然允许有效地检索分子短于50bp。在这里,我们将这些改进应用于植物标本标本的DNA提取方案,并通过霰弹枪测序评估提取性能,这允许准确地估计DNA片段长度的分布。与甲苯甲酸三甲基铵溴(CTAB)相比,用N-苯三噻唑硫化物(PTB)缓冲液中的中值碎片长度降低35%;将DNA的结合条件改性为二氧化硅,允许额外的降低10%。我们没有观察到单链DNA(SSDNA)与双链DNA(DSDNA)文库制备方法进行进一步降低。我们的协议使得从Bbarium标本中检索超短的超级分子,这将有助于解锁储存在豆根草丛中的遗传信息。

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