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Road blocks on paleogenomes—polymerase extension profiling reveals the frequency of blocking lesions in ancient DNA

机译:古基因组学上的障碍-聚合酶延伸谱揭示了古代DNA中阻断病变的频率

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摘要

Although the last few years have seen great progress in DNA sequence retrieval from fossil specimens, some of the characteristics of ancient DNA remain poorly understood. This is particularly true for blocking lesions, i.e. chemical alterations that cannot be bypassed by DNA polymerases and thus prevent amplification and subsequent sequencing of affected molecules. Some studies have concluded that the vast majority of ancient DNA molecules carry blocking lesions, suggesting that the removal, repair or bypass of blocking lesions might dramatically increase both the time depth and geographical range of specimens available for ancient DNA analysis. However, previous studies used very indirect detection methods that did not provide conclusive estimates on the frequency of blocking lesions in endogenous ancient DNA. We developed a new method, polymerase extension profiling (PEP), that directly reveals occurrences of polymerase stalling on DNA templates. By sequencing thousands of single primer extension products using PEP methodology, we have for the first time directly identified blocking lesions in ancient DNA on a single molecule level. Although we found clear evidence for blocking lesions in three out of four ancient samples, no more than 40% of the molecules were affected in any of the samples, indicating that such modifications are far less frequent in ancient DNA than previously thought.
机译:尽管最近几年在从化石标本中检索DNA序列方面取得了长足进步,但对古代DNA的某些特征仍然知之甚少。对于阻断损伤,即DNA聚合酶不能绕过的化学改变,从而阻止受影响的分子的扩增和随后的测序,尤其如此。一些研究得出的结论是,绝大多数古代DNA分子带有封闭性病变,这表明去除,修复或绕过封闭性病变可能会大大增加用于古代DNA分析的标本的时间深度和地理范围。但是,先前的研究使用的是非常间接的检测方法,并未对封闭内源性古代DNA中损伤的频率提供结论性的估计。我们开发了一种新方法,聚合酶延伸分析(PEP),可直接揭示DNA模板上发生聚合酶停滞的情况。通过使用PEP方法对数千个单引物延伸产物进行测序,我们首次在单个分子水平上直接鉴定了古代DNA中的封闭性病变。尽管我们发现了四分之三的古代样本中有明显的阻断病变的证据,但在任何样本中受影响的分子均不超过40%,这表明在古代DNA中这种修饰的发生频率比以前认为的要少得多。

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