Millennia-old coral holobiont DNA provides insight into future adaptive trajectories

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Carly B. Scott, Anny Cárdenas, Matthew Mah, Vagheesh M. Narasimhan, Nadin Rohland, Lauren T. Toth, Christian R. Voolstra, David Reich, Mikhail V. Matz
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引用次数: 1

Abstract

Ancient DNA (aDNA) has been applied to evolutionary questions across a wide variety of taxa. Here, for the first time, we utilized aDNA from millennia-old fossil coral fragments to gain new insights into a rapidly declining western Atlantic reef ecosystem. We sampled four Acropora palmata fragments (dated 4215 BCE to 1099 CE) obtained from two Florida Keys reef cores. From these samples, we established that it is possible both to sequence aDNA from reef cores and place the data in the context of modern-day genetic variation. We recovered varying amounts of nuclear DNA exhibiting the characteristic signatures of aDNA from the A. palmata fragments. To describe the holobiont sensu lato, which plays a crucial role in reef health, we utilized metagenome-assembled genomes as a reference to identify a large additional proportion of ancient microbial DNA from the samples. The samples shared many common microbes with modern-day coral holobionts from the same region, suggesting remarkable holobiont stability over time. Despite efforts, we were unable to recover ancient Symbiodiniaceae reads from the samples. Comparing the ancient A. palmata data to whole-genome sequencing data from living acroporids, we found that while slightly distinct, ancient samples were most closely related to individuals of their own species. Together, these results provide a proof-of-principle showing that it is possible to carry out direct analysis of coral holobiont change over time, which lays a foundation for studying the impacts of environmental stress and evolutionary constraints.

几千年前的珊瑚全息生物DNA提供了对未来适应轨迹的洞察
古DNA (aDNA)已被应用于各种分类群的进化问题。在这里,我们第一次利用来自几千年前的化石珊瑚碎片的aDNA来获得对快速下降的西大西洋珊瑚礁生态系统的新见解。我们从两个佛罗里达礁岛岩心中采集了4块掌肢Acropora palmata碎片(公元前4215年至公元1099年)。从这些样本中,我们确定了对珊瑚礁核心的aDNA进行测序并将数据置于现代遗传变异的背景下是可能的。我们从掌藻碎片中恢复了不同数量的核DNA,显示出aDNA的特征特征。为了描述在珊瑚礁健康中起关键作用的全息生物感知,我们利用宏基因组组装的基因组作为参考,从样本中鉴定了大量额外的古代微生物DNA。这些样本与来自同一地区的现代珊瑚全息生物有许多共同的微生物,这表明随着时间的推移,全息生物具有显著的稳定性。尽管付出了努力,我们还是无法从样本中恢复共生科的古老读数。将古代A. palmata的数据与现存acroporids的全基因组测序数据进行比较,我们发现,尽管古代样本略有不同,但它们与自己物种的个体关系最为密切。总之,这些结果提供了一个原理证明,表明可以对珊瑚全息生物随时间的变化进行直接分析,这为研究环境压力和进化约束的影响奠定了基础。
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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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