Pearman William S, Arranz Vanessa, Carvajal Jose I, Whibley Annabel, Liau Yusmiati, Johnson Katherine, Gray Rachel, Treece Jackson M, Gemmell Neil J, Liggins Libby, Fraser Ceridwen I, Jensen Evelyn L, Green Nicholas J
Department of Marine Science, University of Otago, Dunedin, New Zealand.
School of Biological Sciences, The University of Auckland, Auckland, New Zealand.
J Phycol. 2024 Dec;60(6):1601-1610. doi: 10.1111/jpy.13513. Epub 2024 Oct 22.
Genomic resources have yielded unprecedented insights into ecological and evolutionary processes, not to mention their importance in economic and conservation management of specific organisms. However, the field of macroalgal genomics is hampered by difficulties in the isolation of suitable DNA. Even when DNA that appears high quality by standard metrics has been isolated, such samples may not perform well during the sequencing process. We here have compared Oxford Nanopore long-read sequencing results for three species of macroalgae to those of nonmacroalgal species and determined that when using macroalgal samples, sequencing activity declined rapidly, resulting in reduced sequencing yield. Chemical analysis of macroalgal DNA that would be considered suitable for sequencing revealed that DNA derived from dried macroalgae was enriched for polyphenol-DNA adducts (DNA with large polyphenols chemically attached to it), which may have led to sequencing inhibition. Of note, we observed the strongest evidence of sequencing inhibition and reduced sequence output when using samples dried using silica gel-suggesting that such storage approaches may not be appropriate for samples destined for Oxford Nanopore sequencing. Our findings have wide-ranging implications for the generation of genomic resources from macroalgae and suggest a need to develop new storage methods that are more amenable to Oxford Nanopore sequencing or to use fresh flash-frozen tissue wherever possible for genome sequencing.
基因组资源为生态和进化过程带来了前所未有的见解,更不用说它们在特定生物的经济和保护管理中的重要性了。然而,大型藻类基因组学领域受到合适DNA分离困难的阻碍。即使通过标准指标看起来质量很高的DNA被分离出来,这些样本在测序过程中可能也表现不佳。我们在此将三种大型藻类的牛津纳米孔长读长测序结果与非大型藻类物种的结果进行了比较,确定在使用大型藻类样本时,测序活性迅速下降,导致测序产量降低。对被认为适合测序的大型藻类DNA进行化学分析发现,来自干燥大型藻类的DNA富含多酚-DNA加合物(化学附着有大量多酚的DNA),这可能导致了测序抑制。值得注意的是,当使用硅胶干燥的样本时,我们观察到了最强的测序抑制证据和序列输出减少的情况,这表明这种储存方法可能不适用于用于牛津纳米孔测序的样本。我们的发现对从大型藻类生成基因组资源具有广泛影响,并表明需要开发更适合牛津纳米孔测序的新储存方法,或者尽可能使用新鲜的速冻组织进行基因组测序。