Human endogenous retrovirus K14C drove genomic diversification of the Y chromosome during primate evolution.
Human endogenous retrovirus K14C drove genomic diversification of the Y chromosome during primate evolution.
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人类内源性逆转录病毒 K14C 在灵长类动物进化过程中驱动了 Y 染色体的基因组多样化。
DOI:
10.1038/jhg.2010.94
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发表时间:
2010
期刊:
影响因子:
--
通讯作者:
Namiki M.
中科院分区:
文献类型:
--
作者:
Sin HS;Koh E;Kim DS;Murayama M;Sugimoto K;Maeda Y;Yoshida A;Namiki M.
The male-specific region of Y chromosome (MSY) has accumulated a higher density of human endogenous retroviruses (HERVs) and related sequences when compared with other regions of the human genome. Here, we focused on one HERV family, HERV-K14C that seemed to integrate preferentially into the Y chromosome in humans. To identify every copies of HERV-K14C in the human genome, we applied computational screening to map precisely the locus of individual HERV-K14C copies. Interestingly, 29 of all 146 copies were located in Y chromosome, and these 29 copies were mostly dispersed in the palindromic region. Three distinct HERV-K14C-related transcripts were found and were exclusively expressed in human testis tissue. Based on our phylogenetic analysis of the solitary LTRs derived from HERV-K14C on the Y chromosome we suggested that these sequences were generated as pairs of identical sequences. Specifically, analysis of HERV-K14C-related sequences in the palindromic region demonstrated that the Y chromosomal amplicons existed in our common ancestors and the duplicated pairs arose after divergence of great apes approximately 8–10 million years ago. Taken together, our observation suggested that HERV-K14C-related sequences contributed to genomic diversification of Y chromosome during speciation of great ape lineage.