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Genomic Treasure Troves: Complete Genome Sequencing of Herbarium and Insect Museum Specimens

机译:基因组宝库:植物标本室和昆虫博物馆标本的完整基因组测序

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摘要

Unlocking the vast genomic diversity stored in natural history collections would create unprecedented opportunities for genome-scale evolutionary, phylogenetic, domestication and population genomic studies. Many researchers have been discouraged from using historical specimens in molecular studies because of both generally limited success of DNA extraction and the challenges associated with PCR-amplifying highly degraded DNA. In today's next-generation sequencing (NGS) world, opportunities and prospects for historical DNA have changed dramatically, as most NGS methods are actually designed for taking short fragmented DNA molecules as templates. Here we show that using a standard multiplex and paired-end Illumina sequencing approach, genome-scale sequence data can be generated reliably from dry-preserved plant, fungal and insect specimens collected up to 115 years ago, and with minimal destructive sampling. Using a reference-based assembly approach, we were able to produce the entire nuclear genome of a 43-year-old Arabidopsis thaliana (Brassicaceae) herbarium specimen with high and uniform sequence coverage. Nuclear genome sequences of three fungal specimens of 22–82 years of age (Agaricus bisporus, Laccaria bicolor, Pleurotus ostreatus) were generated with 81.4–97.9% exome coverage. Complete organellar genome sequences were assembled for all specimens. Using de novo assembly we retrieved between 16.2–71.0% of coding sequence regions, and hence remain somewhat cautious about prospects for de novo genome assembly from historical specimens. Non-target sequence contaminations were observed in 2 of our insect museum specimens. We anticipate that future museum genomics projects will perhaps not generate entire genome sequences in all cases (our specimens contained relatively small and low-complexity genomes), but at least generating vital comparative genomic data for testing (phylo)genetic, demographic and genetic hypotheses, that become increasingly more horizontal. Furthermore, NGS of historical DNA enables recovering crucial genetic information from old type specimens that to date have remained mostly unutilized and, thus, opens up a new frontier for taxonomic research as well.
机译:释放自然历史记录中存储的巨大基因组多样性将为基因组规模的进化,系统发育,驯化和种群基因组研究创造前所未有的机会。不鼓励在分子研究中使用历史标本,这是因为DNA提取的成功通常有限,并且与PCR扩增高度降解的DNA相关的挑战也受到限制。在当今的下一代测序(NGS)世界中,历史DNA的机遇和前景发生了巨大变化,因为大多数NGS方法实际上都是为将短片段DNA分子作为模板而设计的。在这里,我们表明,使用标准的多重和配对末端Illumina测序方法,可以可靠地从长达115年前收集的干燥保存的植物,真菌和昆虫标本中可靠地生成基因组规模的序列数据,并且破坏性采样最少。使用基于参考的组装方法,我们能够生产43岁的拟南芥(Brassicaceae)植物标本室标本的完整核基因组,其序列覆盖率高且均匀。生成了三个22–82岁的真菌标本(双孢蘑菇,双花紫菜,平菇)的核基因组序列,外显子覆盖率为81.4–97.9%。为所有标本组装完整的细胞器基因组序列。使用从头组装,我们检索了16.2–71.0%的编码序列区域,因此对于从历史标本中进行从头组装基因组的前景保持谨慎。在我们的两个昆虫博物馆标本中观察到非目标序列污染。我们预计未来的博物馆基因组计划可能不会在所有情况下都生成完整的基因组序列(我们的标本包含相对较小且复杂度较低的基因组),但至少会生成至关重要的比较基因组数据,以测试(系统)遗传,人口统计学和遗传假设,变得越来越水平。此外,历史DNA的NGS能够从迄今为止仍未得到利用的旧样本中恢复重要的遗传信息,因此也为分类学研究开辟了新的领域。

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