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从植物标本馆标本中提取的 DNA 的损伤和衰变动力学的时间模式。

Temporal patterns of damage and decay kinetics of DNA retrieved from plant herbarium specimens.

机构信息

Research Group for Ancient Genomics and Evolution, Department of Molecular Biology , Max Planck Institute for Developmental Biology , Tuebingen 72076 , Germany.

Institute of Archaeological Sciences , University of Tübingen , Tuebingen 72076 , Germany.

出版信息

R Soc Open Sci. 2016 Jun 22;3(6):160239. doi: 10.1098/rsos.160239. eCollection 2016 Jun.

Abstract

Herbaria archive a record of changes of worldwide plant biodiversity harbouring millions of specimens that contain DNA suitable for genome sequencing. To profit from this resource, it is fundamental to understand in detail the process of DNA degradation in herbarium specimens. We investigated patterns of DNA fragmentation and nucleotide misincorporation by analysing 86 herbarium samples spanning the last 300 years using Illumina shotgun sequencing. We found an exponential decay relationship between DNA fragmentation and time, and estimated a per nucleotide fragmentation rate of 1.66 × 10(-4) per year, which is six times faster than the rate estimated for ancient bones. Additionally, we found that strand breaks occur specially before purines, and that depurination-driven DNA breakage occurs constantly through time and can to a great extent explain decreasing fragment length over time. Similar to what has been found analysing ancient DNA from bones, we found a strong correlation between the deamination-driven accumulation of cytosine to thymine substitutions and time, which reinforces the importance of substitution patterns to authenticate the ancient/historical nature of DNA fragments. Accurate estimations of DNA degradation through time will allow informed decisions about laboratory and computational procedures to take advantage of the vast collection of worldwide herbarium specimens.

摘要

标本馆档案记录了全球植物生物多样性的变化,其中蕴藏着数以百万计的标本,这些标本含有适合基因组测序的 DNA。为了充分利用这一资源,必须详细了解标本馆标本中 DNA 降解的过程。我们通过使用 Illumina shotgun 测序分析了跨越过去 300 年的 86 个标本馆样本,研究了 DNA 片段化和核苷酸错配的模式。我们发现 DNA 片段化与时间之间存在指数衰减关系,并估计每个核苷酸的片段化率为每年 1.66×10(-4),这比从古代骨骼中估计的速度快六倍。此外,我们发现链断裂特别发生在嘌呤之前,并且去嘌呤驱动的 DNA 断裂随着时间的推移不断发生,在很大程度上可以解释随时间推移片段长度的减少。与从骨骼中分析古代 DNA 时发现的情况类似,我们发现脱氨作用导致的胞嘧啶向胸腺嘧啶取代与时间之间存在很强的相关性,这加强了取代模式对验证 DNA 片段的古老/历史性质的重要性。对随时间推移的 DNA 降解进行准确估计,将有助于做出明智的决策,选择实验室和计算程序,以充分利用全球标本馆的大量标本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/4929915/e70a3ceb9f7e/rsos160239-g1.jpg

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