一种新的基于复制捕获的方法,用于未知逆转录事件的测序。

IF 4.7 2区 生物学 Q1 GENETICS & HEREDITY Mobile DNA Pub Date : 2020-12-14 DOI:10.1186/s13100-020-00228-6
Alexander Y Komkov, Shamil Z Urazbakhtin, Maria V Saliutina, Ekaterina A Komech, Yuri A Shelygin, Gaiaz A Nugmanov, Vitaliy P Shubin, Anastasia O Smirnova, Mikhail Y Bobrov, Alexey S Tsukanov, Anastasia V Snezhkina, Anna V Kudryavtseva, Yuri B Lebedev, Ilgar Z Mamedov
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引用次数: 2

摘要

背景:逆转录因子(REs)在包括人类在内的所有真核生物基因组中占有重要的一部分。人类基因组中的大多数逆转录因子是无活性的,不能反转录转座。在大多数正常组织中,数十个活性拷贝通过各种细胞机制受到抑制。这些拷贝可以在正常的种系和脑组织或癌症中变得活跃,导致新的逆转录事件。这些事件的后果及其在正常细胞功能和癌变中的作用尚不完全清楚。如果新的插入发生在一小部分细胞中,则只能使用基于RE富集和高通量测序的特定方法来发现。这种方法的高灵敏度的缺点是存在模仿真实插入的各种伪影,在许多情况下,由于缺乏初始模板DNA而无法验证。结果:在这里,我们描述了一种新的复制捕获技术,我们在一种称为逆转录事件未知测序的方法中实现了一种新的复制捕获技术,该技术允许有效和可靠地识别新的基因组RE插入。该方法基于目标分子拷贝的捕获(拷贝捕获),选择性扩增和两侧活性RE插入邻近的基因组区域测序。重要的是,模板基因组DNA保持完整,可以用于验证实验。此外,我们应用了一种新的系统来测试方法的灵敏度,并精确地显示了所开发的方法能够可靠地检测到100个细胞中有1个细胞中的插入,以及1000个细胞中有1个细胞中的大部分插入。利用该方法的优势,我们发现在携带肿瘤特异性L1HS插入的结直肠癌样本中没有体细胞Alu插入。结论:本研究首次描述和实现了复制捕获技术,并为定量评估一小部分细胞中的RE插入提供了第一个方法学基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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SeqURE - a new copy-capture based method for sequencing of unknown Retroposition events.

Background: Retroelements (REs) occupy a significant part of all eukaryotic genomes including humans. The majority of retroelements in the human genome are inactive and unable to retrotranspose. Dozens of active copies are repressed in most normal tissues by various cellular mechanisms. These copies can become active in normal germline and brain tissues or in cancer, leading to new retroposition events. The consequences of such events and their role in normal cell functioning and carcinogenesis are not yet fully understood. If new insertions occur in a small portion of cells they can be found only with the use of specific methods based on RE enrichment and high-throughput sequencing. The downside of the high sensitivity of such methods is the presence of various artifacts imitating real insertions, which in many cases cannot be validated due to lack of the initial template DNA. For this reason, adequate assessment of rare (< 1%) subclonal cancer specific RE insertions is complicated.

Results: Here we describe a new copy-capture technique which we implemented in a method called SeqURE for Sequencing Unknown of Retroposition Events that allows for efficient and reliable identification of new genomic RE insertions. The method is based on the capture of copies of target molecules (copy-capture), selective amplification and sequencing of genomic regions adjacent to active RE insertions from both sides. Importantly, the template genomic DNA remains intact and can be used for validation experiments. In addition, we applied a novel system for testing method sensitivity and precisely showed the ability of the developed method to reliably detect insertions present in 1 out of 100 cells and a substantial portion of insertions present in 1 out of 1000 cells. Using advantages of the method we showed the absence of somatic Alu insertions in colorectal cancer samples bearing tumor-specific L1HS insertions.

Conclusions: This study presents the first description and implementation of the copy-capture technique and provides the first methodological basis for the quantitative assessment of RE insertions present in a small portion of cells.

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来源期刊
Mobile DNA
Mobile DNA GENETICS & HEREDITY-
CiteScore
8.20
自引率
6.10%
发文量
26
审稿时长
11 weeks
期刊介绍: Mobile DNA is an online, peer-reviewed, open access journal that publishes articles providing novel insights into DNA rearrangements in all organisms, ranging from transposition and other types of recombination mechanisms to patterns and processes of mobile element and host genome evolution. In addition, the journal will consider articles on the utility of mobile genetic elements in biotechnological methods and protocols.
期刊最新文献
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