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Insertionally polymorphic sites of human endogenous retrovirus-K (HML-2) with long target site duplications

BACKGROUND: Human endogenous retroviruses (HERVs) belong to the LTR-retrotransposon family, where the complete HERV sequence contains two long terminal repeats (LTRs) located at each end. Intact LTRs possess highly conserved transcriptional promoter and enhancer sequences, so analyses of HERV insert...

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Autores principales: Kahyo, Tomoaki, Yamada, Hidetaka, Tao, Hong, Kurabe, Nobuya, Sugimura, Haruhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488345/
https://www.ncbi.nlm.nih.gov/pubmed/28655292
http://dx.doi.org/10.1186/s12864-017-3872-6
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author Kahyo, Tomoaki
Yamada, Hidetaka
Tao, Hong
Kurabe, Nobuya
Sugimura, Haruhiko
author_facet Kahyo, Tomoaki
Yamada, Hidetaka
Tao, Hong
Kurabe, Nobuya
Sugimura, Haruhiko
author_sort Kahyo, Tomoaki
collection PubMed
description BACKGROUND: Human endogenous retroviruses (HERVs) belong to the LTR-retrotransposon family, where the complete HERV sequence contains two long terminal repeats (LTRs) located at each end. Intact LTRs possess highly conserved transcriptional promoter and enhancer sequences, so analyses of HERV insertional polymorphisms are expected to provide greater insights into human genomic variation compared with the conventional analysis of single nucleotide variations. High-throughput sequencing technology is developing but genome-wide investigations of HERVs are methodically challenging, and thus a comprehensive understanding of HERV insertional polymorphisms and target site duplications (TSDs) remains elusive. RESULTS: We identified five human-specific insertionally polymorphic sites in HERVK (HML-2), one of the HERV subgroups, by extracting HML-2-deleted sequences from the genomic structural variation database, which we successfully characterized and then updated the existing catalogue of HML-2 insertional polymorphisms. The insertionally polymorphic states were confirmed in a small Japanese population by genomic PCR analysis for four of the five sites identified. Sequencing of the preintegration sites clearly showed that the HML-2 site located at 7p21.2 had 250-base pair (bp) TSDs, which is one of the longest TSDs in HML-2. In addition to these five sites, another insertionally polymorphic site for a non-human-specific HML-2 site was also identified at 6p25.2, which was flanked by 111-bp TSDs and the corresponding ERV locus was also annotated in the genome of non-human primates. CONCLUSIONS: Our analysis demonstrated the existence of HERV insertions flanked by unconventionally long TSDs, including those with lengths as high as 250 bp. This suggests that the length range of retroviral TSDs is larger than considered previously, which might help to understand how retroviral integration occurs in the host genome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3872-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-54883452017-07-03 Insertionally polymorphic sites of human endogenous retrovirus-K (HML-2) with long target site duplications Kahyo, Tomoaki Yamada, Hidetaka Tao, Hong Kurabe, Nobuya Sugimura, Haruhiko BMC Genomics Research Article BACKGROUND: Human endogenous retroviruses (HERVs) belong to the LTR-retrotransposon family, where the complete HERV sequence contains two long terminal repeats (LTRs) located at each end. Intact LTRs possess highly conserved transcriptional promoter and enhancer sequences, so analyses of HERV insertional polymorphisms are expected to provide greater insights into human genomic variation compared with the conventional analysis of single nucleotide variations. High-throughput sequencing technology is developing but genome-wide investigations of HERVs are methodically challenging, and thus a comprehensive understanding of HERV insertional polymorphisms and target site duplications (TSDs) remains elusive. RESULTS: We identified five human-specific insertionally polymorphic sites in HERVK (HML-2), one of the HERV subgroups, by extracting HML-2-deleted sequences from the genomic structural variation database, which we successfully characterized and then updated the existing catalogue of HML-2 insertional polymorphisms. The insertionally polymorphic states were confirmed in a small Japanese population by genomic PCR analysis for four of the five sites identified. Sequencing of the preintegration sites clearly showed that the HML-2 site located at 7p21.2 had 250-base pair (bp) TSDs, which is one of the longest TSDs in HML-2. In addition to these five sites, another insertionally polymorphic site for a non-human-specific HML-2 site was also identified at 6p25.2, which was flanked by 111-bp TSDs and the corresponding ERV locus was also annotated in the genome of non-human primates. CONCLUSIONS: Our analysis demonstrated the existence of HERV insertions flanked by unconventionally long TSDs, including those with lengths as high as 250 bp. This suggests that the length range of retroviral TSDs is larger than considered previously, which might help to understand how retroviral integration occurs in the host genome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3872-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-27 /pmc/articles/PMC5488345/ /pubmed/28655292 http://dx.doi.org/10.1186/s12864-017-3872-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kahyo, Tomoaki
Yamada, Hidetaka
Tao, Hong
Kurabe, Nobuya
Sugimura, Haruhiko
Insertionally polymorphic sites of human endogenous retrovirus-K (HML-2) with long target site duplications
title Insertionally polymorphic sites of human endogenous retrovirus-K (HML-2) with long target site duplications
title_full Insertionally polymorphic sites of human endogenous retrovirus-K (HML-2) with long target site duplications
title_fullStr Insertionally polymorphic sites of human endogenous retrovirus-K (HML-2) with long target site duplications
title_full_unstemmed Insertionally polymorphic sites of human endogenous retrovirus-K (HML-2) with long target site duplications
title_short Insertionally polymorphic sites of human endogenous retrovirus-K (HML-2) with long target site duplications
title_sort insertionally polymorphic sites of human endogenous retrovirus-k (hml-2) with long target site duplications
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488345/
https://www.ncbi.nlm.nih.gov/pubmed/28655292
http://dx.doi.org/10.1186/s12864-017-3872-6
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