Human-Specific HERV-K Insertion Causes Genomic Variations in the Human Genome

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Abstract

Human endogenous retroviruses (HERV) sequences account for about 8% of the human genome. Through comparative genomics and literature mining, we identified a total of 29 human-specific HERV-K insertions. We characterized them focusing on their structure and flanking sequence. The results showed that four of the human-specific HERV-K insertions deleted human genomic sequences via non-classical insertion mechanisms. Interestingly, two of the human-specific HERV-K insertion loci contained two HERV-K internals and three LTR elements, a pattern which could be explained by LTR-LTR ectopic recombination or template switching. In addition, we conducted a polymorphic test and observed that twelve out of the 29 elements are polymorphic in the human population. In conclusion, human-specific HERV-K elements have inserted into human genome since the divergence of human and chimpanzee, causing human genomic changes. Thus, we believe that human-specific HERV-K activity has contributed to the genomic divergence between humans and chimpanzees, as well as within the human population. © 2013 Shin et al.

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Shin, W., Lee, J., Son, S. Y., Ahn, K., Kim, H. S., & Han, K. (2013). Human-Specific HERV-K Insertion Causes Genomic Variations in the Human Genome. PLoS ONE, 8(4). https://doi.org/10.1371/journal.pone.0060605

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