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High-Throughput Targeted Repeat Element Bisulfite Sequencing (HT-TREBS): Genome-Wide DNA Methylation Analysis of IAP LTR Retrotransposon

机译:高通量靶向重复元素亚硫酸氢盐测序(HT-TREBS):IAP LTR反转录转座子的全基因组DNA甲基化分析

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摘要

In vertebrates, DNA methylation-mediated repression of retrotransposons is essential for the maintenance of genomic integrity. In the current study, we developed a technique termed HT-TREBS (High-Throughput Targeted Repeat Element Bisulfite Sequencing). This technique is designed to measure the DNA methylation levels of individual loci of any repeat families with next-generation sequencing approaches. To test the feasibility of HT-TREBS, we analyzed the DNA methylation levels of the IAP LTR family using a set of 12 different genomic DNA isolated from the brain, liver and kidney of 4 one-week-old littermates of the mouse strain C57BL/6N. This technique has successfully generated the CpG methylation data of 5,233 loci common in all the samples, representing more than 80% of the individual loci of the five targeted subtypes of the IAP LTR family. According to the results, approximately 5% of the IAP LTR loci have less than 80% CpG methylation levels with no genomic position preference. Further analyses of the IAP LTR loci also revealed the presence of extensive DNA methylation variations between different tissues and individuals. Overall, these data demonstrate the efficiency and robustness of the new technique, HT-TREBS, and also provide new insights regarding the genome-wide DNA methylation patterns of the IAP LTR repeat elements.
机译:在脊椎动物中,DNA甲基化介导的逆转座子阻遏对于维持基因组完整性至关重要。在当前的研究中,我们开发了一种称为HT-TREBS(高通量靶向重复元素亚硫酸氢盐测序)的技术。此技术旨在通过下一代测序方法测量任何重复家族的单个基因座的DNA甲基化水平。为了测试HT-TREBS的可行性,我们使用了12种不同基因组DNA的集合,分析了IAP LTR家族的DNA甲基化水平,这些基因组DNA分离自小鼠品系C57BL / 4个一周龄同窝仔的脑,肝和肾。 6N。此技术已成功生成了所有样品中共有的5,233个基因座的CpG甲基化数据,占IAP LTR家族五个靶向亚型的单个基因座的80%以上。根据结果​​,大约5%的IAP LTR位点的CpG甲基化水平低于80%,并且没有基因组位置偏爱。对IAP LTR基因座的进一步分析还揭示了不同组织和个体之间存在广泛的DNA甲基化变异。总体而言,这些数据证明了新技术HT-TREBS的效率和鲁棒性,还提供了有关IAP LTR重复元件的全基因组DNA甲基化模式的新见解。

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