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    Unbiased optical mapping of telomere-integrated endogenous human herpesvirus 6 (2020)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Wight, Darren J. (WE 5)
    Aimola, Giulia (WE 5)
    Aswad, Amr (WE 5)
    Jill Lai, Chi-Yu
    Bahamon, Christian
    Hong, Karl
    Hill, Joshua A.
    Kaufer, Benedikt B. (WE 5)
    Quelle
    Proceedings of the National Academy of Sciences of the United States of America
    Bandzählung: 117
    Heftzählung: 49
    Seiten: 31410 – 31416
    ISSN: 1091-6490
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://www.pnas.org/content/117/49/31410
    DOI: 10.1073/pnas.2011872117
    Pubmed: 33229517
    Kontakt
    Institut für Virologie

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51833
    virologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    Next-generation sequencing technologies allowed sequencing of thousands of genomes. However, there are genomic regions that remain difficult to characterize, including telomeres, centromeres, and other low-complexity regions, as well as transposable elements and endogenous viruses. Human herpesvirus 6A and 6B (HHV-6A and HHV-6B) are closely related viruses that infect most humans and can integrate their genomes into the telomeres of infected cells. Integration also occurs in germ cells, meaning that the virus can be inherited and result in individuals harboring the virus in every cell of their body. The integrated virus can reactivate and cause disease in humans. While it is well established that the virus resides in the telomere region, the integration locus is poorly defined due to the low sequence complexity (TTAGGG)n of telomeres that cannot be easily resolved through sequencing. We therefore employed genome imaging of the integrated HHV-6A and HHV-6B genomes using whole-genome optical site mapping technology. Using this technology, we identified which chromosome arm harbors the virus genome and obtained a high-resolution map of the integration loci of multiple patients. Surprisingly, this revealed long telomere sequences at the virus-subtelomere junction that were previously missed using PCR-based approaches. Contrary to what was previously thought, our technique revealed that the telomere lengths of chromosomes harboring the integrated virus genome were comparable to the other chromosomes. Taken together, our data shed light on the genetic structure of the HHV-6A and HHV-6B integration locus, demonstrating the utility of optical mapping for the analysis of genomic regions that are difficult to sequence.