Buzdin Anton, Khodosevich Konstantin, Mamedov Ilgar, Vinogradova Tatyana, Lebedev Yuri, Hunsmann Gerhard, Sverdlov Eugene
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10 Miklukho-Maklaya, Moscow, 117997, Russia.
Genomics. 2002 Mar;79(3):413-22. doi: 10.1006/geno.2002.6705.
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.
我们开发了一种靶向基因组差异分析(TGDA)方法,用于全基因组检测密切相关基因组之间散布重复序列整合位点的差异。该方法包括对比较中的两个基因组DNA中与目标散布重复元件相邻的侧翼进行全基因组扩增,以及对选定扩增子进行消减杂交(SH)。通过检测人类和黑猩猩基因组之间人类内源性逆转录病毒K(HERV-K)及相关孤立长末端重复序列(LTR)整合位点的差异,证明了TGDA的潜力。在一个富含人类特异性整合(HSI)位点的文库中随机测序的55个克隆中,33个(60%)代表HSI。所有人类特异性(Hs)LTR均属于两个相关的进化上年轻的群体,这表明在人科谱系中有两个主基因同时活跃。对25名无关的高加索个体的LTR HSI未检测到缺失/插入多态性。我们还讨论了TGDA研究可能的研究应用。