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本文引用的文献

1
Recalibrating Equus evolution using the genome sequence of an early Middle Pleistocene horse.利用早期中更新世马的基因组序列重新校准马的进化。
Nature. 2013 Jul 4;499(7456):74-8. doi: 10.1038/nature12323. Epub 2013 Jun 26.
2
Single-stranded DNA library preparation for the sequencing of ancient or damaged DNA.单链 DNA 文库制备用于测序古老或受损的 DNA。
Nat Protoc. 2013 Apr;8(4):737-48. doi: 10.1038/nprot.2013.038. Epub 2013 Mar 14.
3
DNA analysis of an early modern human from Tianyuan Cave, China.中国甜元洞早期现代人的 DNA 分析。
Proc Natl Acad Sci U S A. 2013 Feb 5;110(6):2223-7. doi: 10.1073/pnas.1221359110. Epub 2013 Jan 22.
4
MAFFT multiple sequence alignment software version 7: improvements in performance and usability.MAFFT 多序列比对软件版本 7:性能和易用性的改进。
Mol Biol Evol. 2013 Apr;30(4):772-80. doi: 10.1093/molbev/mst010. Epub 2013 Jan 16.
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The half-life of DNA in bone: measuring decay kinetics in 158 dated fossils.骨骼中 DNA 的半衰期:测量 158 个有日期化石的衰减动力学。
Proc Biol Sci. 2012 Dec 7;279(1748):4724-33. doi: 10.1098/rspb.2012.1745. Epub 2012 Oct 10.
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A high-coverage genome sequence from an archaic Denisovan individual.古丹尼索瓦人个体的高覆盖度基因组序列。
Science. 2012 Oct 12;338(6104):222-6. doi: 10.1126/science.1224344. Epub 2012 Aug 30.
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Temporal patterns of nucleotide misincorporations and DNA fragmentation in ancient DNA.古 DNA 中核苷酸错配和 DNA 片段化的时间模式。
PLoS One. 2012;7(3):e34131. doi: 10.1371/journal.pone.0034131. Epub 2012 Mar 30.
8
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Length and GC-biases during sequencing library amplification: a comparison of various polymerase-buffer systems with ancient and modern DNA sequencing libraries.测序文库扩增过程中的长度和 GC 偏倚:各种聚合酶-缓冲系统与古老和现代 DNA 测序文库的比较。
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Analysis of high-throughput ancient DNA sequencing data.高通量古代DNA测序数据的分析
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从中更新世洞穴熊的超短 DNA 片段重建的完整线粒体基因组序列。

Complete mitochondrial genome sequence of a Middle Pleistocene cave bear reconstructed from ultrashort DNA fragments.

机构信息

Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany.

出版信息

Proc Natl Acad Sci U S A. 2013 Sep 24;110(39):15758-63. doi: 10.1073/pnas.1314445110. Epub 2013 Sep 9.

DOI:10.1073/pnas.1314445110
PMID:24019490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3785785/
Abstract

Although an inverse relationship is expected in ancient DNA samples between the number of surviving DNA fragments and their length, ancient DNA sequencing libraries are strikingly deficient in molecules shorter than 40 bp. We find that a loss of short molecules can occur during DNA extraction and present an improved silica-based extraction protocol that enables their efficient retrieval. In combination with single-stranded DNA library preparation, this method enabled us to reconstruct the mitochondrial genome sequence from a Middle Pleistocene cave bear (Ursus deningeri) bone excavated at Sima de los Huesos in the Sierra de Atapuerca, Spain. Phylogenetic reconstructions indicate that the U. deningeri sequence forms an early diverging sister lineage to all Western European Late Pleistocene cave bears. Our results prove that authentic ancient DNA can be preserved for hundreds of thousand years outside of permafrost. Moreover, the techniques presented enable the retrieval of phylogenetically informative sequences from samples in which virtually all DNA is diminished to fragments shorter than 50 bp.

摘要

虽然在古代 DNA 样本中,存活的 DNA 片段数量与其长度之间存在反比关系,但古代 DNA 测序文库中明显缺乏短于 40 个碱基的分子。我们发现,短分子在 DNA 提取过程中可能会丢失,并提出了一种改进的基于二氧化硅的提取方案,可有效回收这些短分子。结合单链 DNA 文库制备,该方法使我们能够从西班牙阿塔普埃斯卡的西玛德洛斯 huesos 挖掘的中更新世洞穴熊(Ursus deningeri)骨中重建线粒体基因组序列。系统发育重建表明,U. deningeri 序列与所有西欧晚更新世洞穴熊形成早期分化的姊妹谱系。我们的结果证明,真正的古代 DNA 可以在永冻层之外保存数十万年。此外,所提出的技术可从几乎所有 DNA 都减少到短于 50 个碱基的片段的样本中检索具有系统发育信息的序列。