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杂交捕获法可用于分析古代海洋真核生物的 DNA 损伤。

Hybridisation capture allows DNA damage analysis of ancient marine eukaryotes.

机构信息

Australian Centre for Ancient DNA, School of Biological Sciences, Faculty of Sciences, The University of Adelaide, Adelaide, SA, Australia.

Institute for Marine and Antarctic Studies, University of Tasmania, Hobart, TAS, Australia.

出版信息

Sci Rep. 2021 Feb 5;11(1):3220. doi: 10.1038/s41598-021-82578-6.

Abstract

Marine sedimentary ancient DNA (sedaDNA) is increasingly used to study past ocean ecosystems, however, studies have been severely limited by the very low amounts of DNA preserved in the subseafloor, and the lack of bioinformatic tools to authenticate sedaDNA in metagenomic data. We applied a hybridisation capture 'baits' technique to target marine eukaryote sedaDNA (specifically, phyto- and zooplankton, 'Planktonbaits1'; and harmful algal bloom taxa, 'HABbaits1'), which resulted in up to 4- and 9-fold increases, respectively, in the relative abundance of eukaryotes compared to shotgun sequencing. We further used the bioinformatic tool 'HOPS' to authenticate the sedaDNA component, establishing a new proxy to assess sedaDNA authenticity, "% eukaryote sedaDNA damage", that is positively correlated with subseafloor depth. We used this proxy to report the first-ever DNA damage profiles from a marine phytoplankton species, the ubiquitous coccolithophore Emiliania huxleyi. Our approach opens new avenues for the detailed investigation of long-term change and evolution of marine eukaryotes over geological timescales.

摘要

海洋沉积物古 DNA(sedanDNA)越来越多地被用于研究过去的海洋生态系统,但由于海底保存的 DNA 量非常少,以及缺乏用于在宏基因组数据中验证 sedaDNA 的生物信息学工具,研究受到了严重限制。我们应用杂交捕获“诱饵”技术来靶向海洋真核 sedaDNA(特别是浮游植物和浮游动物,“浮游生物诱饵 1”;以及有害藻华分类群,“HAB 诱饵 1”),这分别导致真核生物的相对丰度相对于 shotgun 测序增加了 4 倍和 9 倍。我们进一步使用生物信息学工具“HOPS”来验证 sedaDNA 成分,建立了一个新的代理来评估 sedaDNA 的真实性,“%真核 sedaDNA 损伤”,这与海底深度呈正相关。我们使用该代理报告了来自海洋浮游植物物种——无处不在的颗石藻 Emiliania huxleyi 的首个 DNA 损伤谱。我们的方法为在地质时间尺度上详细研究海洋真核生物的长期变化和进化开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/270d/7864908/9d30c0b9dfdc/41598_2021_82578_Fig1_HTML.jpg

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