Evidence map›Paper›PMID 41025794›Full record

ArticleJournal of virology2025

Epigenetic motifs distinguishing endogenous from exogenous retroviral integrants.

Sarah LaMere, Hanbei Xiong, Wei Wang, Brian LaMere, Niema Moshiri

Abstract read
In one paragraph

Article in Journal of virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Sarah LaMereDepartment of Medicine, University of California San Diego, La Jolla, California, USA.ORCID 0000-0002-4612-0425
Hanbei XiongDepartment of Chemistry and Biochemistry, University of California San Diego, La Jolla, California, USA.
Wei WangDepartment of Chemistry and Biochemistry, University of California San Diego, La Jolla, California, USA.
Brian LaMereIndependent Researcher, Escondido, California, USA.
Niema MoshiriDepartment of Computer Science and Engineering, University of California San Diego, La Jolla, California, USA.

Funding

Integrated analysis of genetic variation and epigenomic dataR01HG009626 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WANG, WEI · 2017 to 2025
$4.5M
Epigenetic profiling of HIV-associated neuroinflammation and proviral expression in the brainR01NS137852 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Sarah Adrianne LaMere · 2024 to 2026
$2.4M
Comparative Retroviral EpigenomicsK01OD026565 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LAMERE, SARAH ADRIANNE · 2018 to 2023
$797k
NHGRI NIH HHS R01 HG009626NIH HHS 1K01OD026565NIH HHS K01 OD026565NIH HHS R01HG009626NIH HHS R01NS137852NINDS NIH HHS R01 NS137852
6 · The paper itself

Abstract

Retroviruses are subject to epigenetic regulation by the host genome after integrating, similar to vertebrate genes. However, their patterns of integration, and therefore their likely epigenetic regulation, differ between genera. Beta- and gammaretroviruses are two types of simple retroviruses that have a strong tendency to infect germ cells and endogenize. While ancient endogenous retroviruses are often easy to spot due to mutations rendering them non-functional, more recent integrants can maintain the capacity for full viral production, making it sometimes difficult to discern which integrants are exogenous and likely more clinically relevant. Because endogenous retroviruses generally spend a longer time integrated and subject to host epigenetic regulation as proviral DNA, we hypothesized we could show these integrants exhibit sequence differences from their exogenous counterparts, likely resulting from DNA methylation and histone modifications, and that endogenous retroviruses would generally show habituation to host promoters. Therefore, we have used statistical analyses of publicly available sequence data to demonstrate that endogenous retroviral variants exhibit decreased CpG dinucleotide and altered trinucleotide frequencies over time, and that they will show evidence for loss of motifs associated with "active" histone modifications. Close examination of these patterns provides further clues for distinguishing endogenous and exogenous retroviral variants, potentially aiding in the study of retroviruses in less well-characterized wildlife species. IMPORTANCE: Expression of vertebrate genes is regulated by chemical modifications made directly to the DNA or to the proteins associated with it, termed epigenetics. Because retroviruses integrate into DNA, they are subject to the same epigenetic modifications as regular genes. Retroviruses will tend to endogenize, meaning they will become a permanent part of a species' genome when their hidden DNA is passed down to progeny during reproduction. However, sometimes it is difficult to discern whether a retroviral sequence is endogenous (permanently fixed) or exogenous (an infectious entity). We hypothesized that changes to the retroviral sequences over time after endogenization would result from epigenetic modifications, and that these changes could help distinguish an endogenous retrovirus from an exogenous one. In this paper, we show that changes to the viral sequences associated with epigenetics indeed take place after endogenization.

Indexed as

Endogenous RetrovirusesEpigenesis, GeneticVirus IntegrationAnimalsCpG IslandsDNA MethylationHumansProvirusesDNA methylationendogenous retrovirusepigenetics

Identifiers

PMID41025794
PMCPMC12548410

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.