Evidence map›Paper›PMID 29860323›Full record

ArticleGenome biology and evolution2018

Activity of Genes with Functions in Human Williams-Beuren Syndrome Is Impacted by Mobile Element Insertions in the Gray Wolf Genome.

Bridgett M vonHoldt, Sarah S Ji, Matthew L Aardema, Daniel R Stahler, Monique A R Udell, Janet S Sinsheimer

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2025
    Review
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  8. iScience · 2023
    Article
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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

6 authors at 6 institutions in 1 country.

Bridgett M vonHoldtDepartment of Ecology & Evolutionary Biology, Princeton University, New Jersey.
Sarah S JiDepartment of Biostatistics, UCLA Fielding School of Public Health, Los Angeles, California.
Matthew L AardemaDepartment of Biology, Montclair State University, New Jersey.
Daniel R StahlerYellowstone Center for Resources, National Park Service, Yellowstone National Park, Wyoming.
Monique A R UdellDepartment of Animal & Rangeland Sciences, Oregon State University, Oregon.
Janet S SinsheimerDepartment of Biostatistics, UCLA Fielding School of Public Health, Los Angeles, California.
American Museum of Natural History · USNational Park Service · USOregon State University · USPrinceton University · USUCLA Health · USUniversity of California, Los Angeles · US

Funding

STATISTICAL METHODS FOR GENE MAPPINGR01GM053275 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LANGE, KENNETH L · 1995 to 2019
$9.3M
NIGMS NIH HHS R01 GM053275
6 · The paper itself

Abstract

In canines, transposon dynamics have been associated with a hyper-social behavioral syndrome, although the functional mechanism has yet to be described. We investigate the epigenetic and transcriptional consequences of these behavior-associated mobile element insertions (MEIs) in dogs and Yellowstone gray wolves. We posit that the transposons themselves may not be the causative feature; rather, their transcriptional regulation may exert the functional impact. We survey four outlier transposons associated with hyper-sociability, with the expectation that they are targeted for epigenetic silencing. We predict hyper-methylation of MEIs, suggestive that the epigenetic silencing of and not the MEIs themselves may be driving dysregulation of nearby genes. We found that transposon-derived sequences are significantly hyper-methylated, regardless of their copy number or species. Further, we have assessed transcriptome sequence data and found evidence that MEIs impact the expression levels of six genes (WBSCR17, LIMK1, GTF2I, WBSCR27, BAZ1B, and BCL7B), all of which have known roles in human Williams-Beuren syndrome due to changes in copy number, typically hemizygosity. Although further evidence is needed, our results suggest that a few insertions alter local expression at multiple genes, likely through a cis-regulatory mechanism that excludes proximal methylation.

Indexed as

AnimalsDNA Transposable ElementsDogsEpigenesis, GeneticGene DosageGene Expression RegulationGene SilencingHumansMethylationTranscription, GeneticTranscriptomeWilliams SyndromeWolvesDNA Transposable Elements

Identifiers

PMID29860323
PMCPMC6007319
OpenAlexW2806829006

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.