Evidence map›Paper›PMID 25806706›Full record

ArticleNature communications2015

A family of transposable elements co-opted into developmental enhancers in the mouse neocortex.

James H Notwell, Tisha Chung, Whitney Heavner, Gill Bejerano

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
18.6field-weighted citation impact, top 1% 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

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 113 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Germline hypomethylation shapes dynamic CpG reservoirs in ape genomes.bioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Transposable Elements Co-Option in Genome Evolution and Gene Regulation.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Review

3 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

James H NotwellDepartment of Computer Science, Stanford University, 279 Campus Drive West (MC 5329), Beckman Center B-300, Stanford, California 94305-5329, USA.
Tisha ChungDepartment of Developmental Biology, Stanford University, 279 Campus Drive West (MC 5329), Beckman Center B-300, Stanford, California 94305-5329, USA.
Whitney Heavner1] Department of Developmental Biology, Stanford University, 279 Campus Drive West (MC 5329), Beckman Center B-300, Stanford, California 94305-5329, USA [2] Department of Biology, Stanford University, 279 Campus Drive West (MC 5329), Beckman Center B-300, Stanford, California 94305-5329, USA.ORCID 0000000167094062
Gill Bejerano1] Department of Computer Science, Stanford University, 279 Campus Drive West (MC 5329), Beckman Center B-300, Stanford, California 94305-5329, USA [2] Department of Developmental Biology, Stanford University, 279 Campus Drive West (MC 5329), Beckman Center B-300, Stanford, California 94305-5329, USA [3] Department of Pediatrics, Division of Medical Genetics, Stanford University, 279 Campus Drive West (MC 5329), Beckman Center B-300, Stanford, California 94305-5329, USA.
Stanford University · US

Funding

Combining genetics, genomics, and anatomy to classify cell types across mammalsU01MH105949 · NIMH · BRANDEIS UNIVERSITY · PI BEJERANO, GILL, LOIS, CARLOS · 2014 to 2016
$3.4M
NIMH NIH HHS NIH U01MH105949NIMH NIH HHS U01 MH105949
6 · The paper itself

Abstract

The neocortex is a mammalian-specific structure that is responsible for higher functions such as cognition, emotion and perception. To gain insight into its evolution and the gene regulatory codes that pattern it, we studied the overlap of its active developmental enhancers with transposable element (TE) families and compared this overlap to uniformly shuffled enhancers. Here we show a striking enrichment of the MER130 repeat family among active enhancers in the mouse dorsal cerebral wall, which gives rise to the neocortex, at embryonic day 14.5. We show that MER130 instances preserve a common code of transcriptional regulatory logic, function as enhancers and are adjacent to critical neocortical genes. MER130, a nonautonomous interspersed TE, originates in the tetrapod or possibly Sarcopterygii ancestor, which far predates the appearance of the neocortex. Our results show that MER130 elements were recruited, likely through their common regulatory logic, as neocortical enhancers.

Indexed as

AnimalsDatabases, GeneticDNA Transposable ElementsE1A-Associated p300 ProteinEmbryo, MammalianEnhancer Elements, GeneticEvolution, MolecularGene Expression Regulation, DevelopmentalMiceNeocortexTranscription FactorsDNA Transposable ElementsE1A-Associated p300 ProteinEp300 protein, mouseTranscription Factors

Identifiers

PMID25806706
PMCPMC4438107
OpenAlexW2032496688

What OpenQuestion holds

Textmetadata
LicenceTDM
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.