Evidence map›Paper›PMID 27998931›Full record

ArticleNucleic acids research2017

Human population-specific gene expression and transcriptional network modification with polymorphic transposable elements.

Lu Wang, Lavanya Rishishwar, Leonardo Mariño-Ramírez, I King Jordan

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
12.3field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
  3. TheProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. The landscape of non-reference SINE-VNTR-Alus in amyotrophic lateral sclerosis.Experimental biology and medicine (Maywood, N.J.) · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Observational
  14. Article
  15. Article
  16. Article
  17. Review
  18. Mechanisms of disease-associated SINE-VNTR-Alus.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
  19. Article
  20. Characterisation of the Function of a SINE-VNTR-Frontiers in molecular neuroscience · 2022
    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

4 authors at 2 institutions in 2 countries.

Lu WangSchool of Biology, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Lavanya RishishwarSchool of Biology, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Leonardo Mariño-RamírezPanAmerican Bioinformatics Institute, Cali, Valle del Cauca, 760043, Colombia.
I King JordanSchool of Biology, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Georgia Institute of Technology · USNational Institutes of Health · US

Funding

Genome Assemblies, Analyses, and ComparisonsZIALM082713 · NLM · NATIONAL LIBRARY OF MEDICINE · PI LANDSMAN, DAVID · 2013 to 2025
$3.5M
6 · The paper itself

Abstract

Transposable element (TE) derived sequences are known to contribute to the regulation of the human genome. The majority of known TE-derived regulatory sequences correspond to relatively ancient insertions, which are fixed across human populations. The extent to which human genetic variation caused by recent TE activity leads to regulatory polymorphisms among populations has yet to be thoroughly explored. In this study, we searched for associations between polymorphic TE (polyTE) loci and human gene expression levels using an expression quantitative trait loci (eQTL) approach. We compared locus-specific polyTE insertion genotypes to B cell gene expression levels among 445 individuals from 5 human populations. Numerous human polyTE loci correspond to both cis and trans eQTL, and their regulatory effects are directly related to cell type-specific function in the immune system. PolyTE loci are associated with differences in expression between European and African population groups, and a single polyTE loci is indirectly associated with the expression of numerous genes via the regulation of the B cell-specific transcription factor PAX5. The polyTE-gene expression associations we found indicate that human TE genetic variation can have important phenotypic consequences. Our results reveal that TE-eQTL are involved in population-specific gene regulation as well as transcriptional network modification.

Indexed as

Gene Regulatory NetworksGenome, HumanQuantitative Trait LociBlack PeopleB-LymphocytesCytokinesDNA Transposable ElementsGene Expression RegulationGenetic LociHumansImmunity, InnatePAX5 Transcription FactorPolymorphism, Single NucleotideReceptors, Antigen, T-CellWhite PeopleCytokinesDNA Transposable ElementsPAX5 protein, humanPAX5 Transcription FactorReceptors, Antigen, T-Cell

Identifiers

PMID27998931
PMCPMC5389732
OpenAlexW2565657638

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.