Evidence map›Paper›PMID 33229517›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Unbiased optical mapping of telomere-integrated endogenous human herpesvirus 6.

Darren J Wight, Giulia Aimola, Amr Aswad, Chi-Yu Jill Lai, Christian Bahamon, Karl Hong, Joshua A Hill, Benedikt B Kaufer

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Endogenous human herpesviruses 6A/B.Journal of virology · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. DNA Labeling Using DNA Methyltransferases.Advances in experimental medicine and biology · 2022
    Article
  15. Article
  16. Article
  17. Review
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Darren J WightInstitut für Virologie, Freie Universität Berlin, 14163 Berlin, Germany; d.j.wight@gmail.com b.kaufer@fu-berlin.de.ORCID 0000-0001-6320-5597
Giulia AimolaInstitut für Virologie, Freie Universität Berlin, 14163 Berlin, Germany.ORCID 0000-0002-2793-8512
Amr AswadInstitut für Virologie, Freie Universität Berlin, 14163 Berlin, Germany.ORCID 0000-0002-5776-0057
Chi-Yu Jill LaiBionano Genomics, San Diego, CA 92121.
Christian BahamonBionano Genomics, San Diego, CA 92121.ORCID 0000-0003-2271-8083
Karl HongBionano Genomics, San Diego, CA 92121.
Joshua A HillDepartment of Medicine, University of Washington, Seattle, WA 98195-6420.ORCID 0000-0002-7665-7100
Benedikt B KauferInstitut für Virologie, Freie Universität Berlin, 14163 Berlin, Germany; d.j.wight@gmail.com b.kaufer@fu-berlin.de.ORCID 0000-0003-1328-2695
Freie Universität Berlin · DEBioNano Genomics (United States) · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Optical ImagingChromosomes, HumanGenome, ViralHerpesvirus 6, HumanHost-Pathogen InteractionsHumansTelomereTelomere Homeostasishuman herpesvirus 6iciHHV-6structural genomic mappingtelomere integrationvirus integration

Identifiers

PMID33229517
PMCPMC7733811
OpenAlexW3107343086

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.