Evidence map›Paper›PMID 38690732›Full record

ArticleThe Journal of clinical investigation2024

BAP1 is required prenatally for differentiation and maintenance of postnatal murine enteric nervous system.

Sabine Schneider, Jessica B Anderson, Rebecca P Bradley, Katherine Beigel, Christina M Wright, Beth A Maguire, Guang Yan, Deanne M Taylor, J William Harbour, Robert O Heuckeroth

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2024. 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
1.7field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Whole-Gut Spatial Genomic Analysis Reveals Molecular Regionalization of the Differentiating Zebrafish Enteric Nervous System.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    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

10 authors at 2 institutions in 1 country.

Sabine SchneiderChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
Jessica B AndersonChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
Rebecca P BradleyChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
Katherine BeigelChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
Christina M WrightChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
Beth A MaguireChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
Guang YanChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
Deanne M TaylorChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
J William HarbourDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Robert O HeuckerothChildren's Hospital of Philadelphia Research Institute, Abramson Research Center, Philadelphia, Pennsylvania, USA.
Children's Hospital of Philadelphia · USThe University of Texas Southwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epigenetic regulatory mechanisms are underappreciated, yet are critical for enteric nervous system (ENS) development and maintenance. We discovered that fetal loss of the epigenetic regulator Bap1 in the ENS lineage caused severe postnatal bowel dysfunction and early death in Tyrosinase-Cre Bap1fl/fl mice. Bap1-depleted ENS appeared normal in neonates; however, by P15, Bap1-deficient enteric neurons were largely absent from the small and large intestine of Tyrosinase-Cre Bap1fl/fl mice. Bowel motility became markedly abnormal with disproportionate loss of cholinergic neurons. Single-cell RNA sequencing at P5 showed that fetal Bap1 loss in Tyrosinase-Cre Bap1fl/fl mice markedly altered the composition and relative proportions of enteric neuron subtypes. In contrast, postnatal deletion of Bap1 did not cause enteric neuron loss or impaired bowel motility. These findings suggest that BAP1 is critical for postnatal enteric neuron differentiation and for early enteric neuron survival, a finding that may be relevant to the recently described human BAP1-associated neurodevelopmental disorder.

Indexed as

Cell DifferentiationEnteric Nervous SystemTumor Suppressor ProteinsUbiquitin ThiolesteraseAnimalsFemaleGastrointestinal MotilityHumansMiceMice, KnockoutNeuronsBAP1 protein, mouseTumor Suppressor ProteinsUbiquitin ThiolesteraseDevelopmentGastroenterologyNeurodegeneration

Identifiers

PMID38690732
PMCPMC11060734
OpenAlexW4396531028

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.