Evidence map›Paper›PMID 39957428›Full record

ArticleHuman molecular genetics2025

Functional characterization of OXTR-associated enhancers.

Dianne Laboy Cintrón, Rory R Sheng, Nadav Ahituv

Abstract read
In one paragraph

Article in Human molecular genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Dianne Laboy CintrónDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, 1700 4th St, Byers Hall, San Francisco, CA 94158, United States.
Rory R ShengDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, 1700 4th St, Byers Hall, San Francisco, CA 94158, United States.
Nadav AhituvDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, 1700 4th St, Byers Hall, San Francisco, CA 94158, United States.

Funding

Maximizing Opportunities for Research Excellence - Evaluation Training SupplementR25GM056847 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DUNCAN, D'ANNE S., SELLO, JASON K · 1998 to 2023
$14.1M
Functional characterization of obesity-associated OXTR enhancersR01DK124769 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AHITUV, NADAV, VAISSE, CHRISTIAN · 2020 to 2024
$3.7M
NIDDK NIH HHS 1R01DK124769NIDDK NIH HHS R01 DK124769NIGMS NIH HHS R25GM056847UCSF Discovery Fellowship, and NIDDK 3R01DK124769-04S1UCSF Initiative for Maximizing Student Development Program
6 · The paper itself

Abstract

The oxytocin receptor (OXTR) has a vital role in regulating human behavior, controlling lactation, parturition, pair bonding, maternal behavior, anxiety, and sociability. However, its regulatory elements and how variation in these sequences lead to behavioral changes remain largely unknown. Here, we identified seven OXTR candidate cis-regulatory elements (cCREs) from mouse and human hypothalamus single-cell RNA/ATAC-seq data and characterized them in cells and mice. Luciferase assays in hypothalamus cell lines identified three of the seven to be functional enhancers. Mouse enhancer assays for the most robust enhancer, OXTR candidate enhancer 7 (OCE7), found it to be active in the mouse olfactory bulb at postnatal day 28 and day 56. In summary, using genomic data coupled with cell and mouse enhancer assays, we characterized the OXTR regulatory landscape and identified a novel olfactory bulb OXTR-associated enhancer.

Indexed as

Enhancer Elements, GeneticReceptors, OxytocinAnimalsFemaleHumansHypothalamusMiceOlfactory BulbOxytocinOXTR protein, humanOXTR protein, mouseOxytocinReceptors, Oxytocinenhancergene regulationgeneticsoxytocin receptor

Identifiers

PMID39957428
PMCPMC12056307

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.