人内源性逆转录病毒K家族(HERV-K)染色体长末端重复序列的核苷酸序列和系统发育分析。

H. Kim, J. Y. Choi, W. Lee, K. Jang, B. Hyun
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引用次数: 2

摘要

有研究表明,人类内源性逆转录病毒K家族(HERV-K)在疾病中起作用,HERV-K的孤立长末端重复序列(lts)可能影响位置较近的基因的表达。利用人类单染色体8、9、17和18,用特异性PCR引物鉴定出34个新的HERV-K lts序列。这些LTR元件与人类特异性HERV-K LTR用邻居连接和最大简约法进行系统发育分析。克隆HKL8-5、HKL9-5和HKL9-8与人类特异性HERV-K lts同源性超过99%。9号染色体上的HKL9-5克隆与16号染色体上的人类特异性LTR AC002400序列完全相同。研究结果表明,人类染色体上的HERV-K LTR元件最近出现了增殖、转位或染色体易位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nucleotide sequence and phylogenetic analysis of long terminal repeats of human endogenous retrovirus K family (HERV-K) on human chromosomes.
It has been suggested that human endogenous retroviruses K family (HERV-K) has a role in disease, and solitary long terminal repeats (LTRs) of HERV-K have been potentially capable of affecting the expression of closely located genes. Using the human monochromosomes 8, 9, 17, and 18, with specific PCR primers, we identified thirty-four sequences of new HERV-K LTRs. Those LTR elements were analyzed phylogenetically with the human-specific HERV-K LTRs using neighbor-joining and maximum parsimony methods. Clones HKL8-5, HKL9-5, and HKL9-8 are related by more than 99% homology with the human-specific HERV-K LTRs. The HKL9-5 clone on chromosome 9 was 100% identical with the sequences of human-specific LTR, AC002400, on chromosome 16. The findings suggest that there has been recent proliferation, transposition, or chromosomal translocation of HERV-K LTR elements on human chromosomes.
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