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A technique for genome-wide identification of differences in the interspersed repeats integrations between closely related genomes and its application to detection of human-specific integrations of HERV-K LTRs.

机译:一种用于全基因组识别紧密相关基因组之间的重复重复整合差异的技术,并将其用于检测HERV-K LTR的人特异性整合。

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摘要

We have developed a method of targeted genomic difference analysis (TGDA) for genomewide detection of interspersed repeat integration site differences between closely related genomes. The method includes a whole-genome amplification of the flanks adjacent to target interspersed repetitive elements in both genomic DNAs under comparison, and subtractive hybridization (SH) of the selected amplicons. The potential of TGDA was demonstrated by the detection of differences in the integration sites of human endogenous retroviruses K (HERV-K) and related solitary long terminal repeats (LTRs) between the human and chimpanzee genomes. Of 55 randomly sequenced clones from a library enriched with human-specific integration (HSI) sites, 33 (60%) represented HSIs. All the human-specific (Hs) LTRs belong to two related evolutionarily young groups, suggesting simultaneous activity of two master genes in the hominid lineage. No deletion/insertion polymorphism was detected for the LTR HSIs for 25 unrelated caucasoid individuals. We also discuss the possible research applications for TGDA research.
机译:我们已经开发了一种靶向基因组差异分析(TGDA)的方法,可用于在全基因组范围内检测紧密相关的基因组之间散布的重复整合位点差异。该方法包括在比较中的两个基因组DNA中与目标散布的重复元件相邻的侧翼进行全基因组扩增,以及所选扩增子的减性杂交(SH)。 TGDA的潜力已通过检测人类内源性逆转录病毒K(HERV-K)和人类与黑猩猩基因组之间相关的孤立长末端重复序列(LTR)整合位点的差异而得到证明。来自富集人特异性整合(HSI)位点的文库的55个随机测序的克隆中,有33个(60%)代表HSI。所有人类特异的(Hs)LTR都属于两个相关的进化年轻群体,表明在原始人类谱系中同时存在两个主基因的活性。没有检测到25个无关的高加索人的LTR HSI的删除/插入多态性。我们还将讨论TGDA研究的可能研究应用。

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