Evidence map›Paper›PMID 41920822›Full record

ArticlePLoS genetics2026

ADNP regulates chromatin architecture and lineage fidelity during neural differentiation.

Phillip Wulfridge, Nathaniel Rell, John Doherty, Kuo-Chen Fang, Michelle Lee Lynskey, Kavitha Sarma

Abstract read
In one paragraph

Article in PLoS genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Phillip WulfridgeGene expression and Regulation program, The Wistar Institute, Philadelphia, Pennsylvania, United States of America.
Nathaniel RellGene expression and Regulation program, The Wistar Institute, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0009-0003-8125-1564
John DohertyGene expression and Regulation program, The Wistar Institute, Philadelphia, Pennsylvania, United States of America.
Kuo-Chen FangGene expression and Regulation program, The Wistar Institute, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0009-0007-3430-2081
Michelle Lee LynskeyGene expression and Regulation program, The Wistar Institute, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-0343-3413
Kavitha SarmaGene expression and Regulation program, The Wistar Institute, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-3045-210X

Funding

TRAINING PROGRAM IN BASIC CANCER RESEARCHT32CA009171 · NCI · WISTAR INSTITUTE · PI Alessandro Gardini · 1985 to 2026
$15.3M
CTCF-dependent mechanisms of ATRX in neuronal differentiationR01NS127828 · NINDS · WISTAR INSTITUTE · PI Kavitha Sarma · 2022 to 2026
$2.6M
ADNP mechanisms in R-loop regulation during differentiationR01GM143229 · NIGMS · WISTAR INSTITUTE · PI SARMA, KAVITHA · 2022 to 2025
$1.7M
R-loop functions in neuronal gene expression and genome organizationR01NS135217 · NINDS · WISTAR INSTITUTE · PI Kavitha Sarma · 2024 to 2026
$1.5M
The role of non-canonical nucleic acid structures in genome regulationR35GM161559 · NIGMS · WISTAR INSTITUTE · PI Kavitha Sarma · 2026 to 2026
$363k
NCI NIH HHS T32 CA009171NIGMS NIH HHS R01 GM143229NIGMS NIH HHS R35 GM161559NINDS NIH HHS R01 NS127828NINDS NIH HHS R01 NS135217
6 · The paper itself

Abstract

Transition from a pluripotent to a differentiated cell state is accompanied by significant changes in genome organization. Activity dependent neuroprotective protein (ADNP) is a chromatin regulator with critical roles in neurodevelopment and limits the genomic occupancy of CTCF, a master architectural protein in genome organization, in embryonic stem cells. However, ADNP localization, function, and relationship with CTCF in differentiated neural lineages are not well studied. Here we develop a dual degron model which allows us to acutely deplete ADNP in neural progenitor cells (NPCs). We find that ADNP depletion does not impact NPC survival in the short term, but results in a genome organization switch, which favors the formation of short-range chromatin looping interactions coinciding with CTCF accumulation. Furthermore, ADNP localizes to active gene promoters in NPCs that are unoccupied by CTCF, where it prevents over-expression of genes that are activated upon neurodifferentiation and represses those involved in commitment to other lineages. Our findings uncover CTCF-dependent as well as CTCF-independent regulatory mechanisms of ADNP in NPC-specific chromatin organization and gene expression programs that may underlie its essential function in neurodevelopment.

Indexed as

Cell DifferentiationChromatinNerve Tissue ProteinsNeural Stem CellsAnimalsCCCTC-Binding FactorCell LineageEmbryonic Stem CellsGene Expression Regulation, DevelopmentalMiceNeurodevelopmentNeurogenesisNeuronsPromoter Regions, GeneticRepressor ProteinsCCCTC-Binding FactorChromatinCtcf protein, mouseNerve Tissue ProteinsRepressor Proteins

Identifiers

PMID41920822
PMCPMC13061322

What Socratic 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 Socratic graph.