Evidence map›Paper›PMID 41540049›Full record

ArticleNature communications2026

Inferring chromatin architecture at a single locus through probabilistic in situ DNA localization.

Minh Tam Le, James McGehee, Leslie Dunipace, David Rumph, Angelike Stathopoulos

Abstract read
In one paragraph

Article in Nature communications, 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. 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

5 authors.

Minh Tam LeDivision of Biology and Biological Engineering, California Institute of Technology, 1200 East California Blvd, Pasadena, CA, USA.ORCID http://orcid.org/0009-0003-4665-7876
James McGeheeDivision of Biology and Biological Engineering, California Institute of Technology, 1200 East California Blvd, Pasadena, CA, USA.ORCID http://orcid.org/0000-0002-9353-1235
Leslie DunipaceDivision of Biology and Biological Engineering, California Institute of Technology, 1200 East California Blvd, Pasadena, CA, USA.ORCID http://orcid.org/0000-0002-1739-6537
David RumphSchmidt Academy for Software Engineering - Office of the Provost, California Institute of Technology, 1200 East California Blvd, Pasadena, CA, USA.
Angelike StathopoulosDivision of Biology and Biological Engineering, California Institute of Technology, 1200 East California Blvd, Pasadena, CA, USA. angelike@caltech.edu.ORCID http://orcid.org/0000-0001-6597-2036

Funding

Temporal control of cell patterning, signaling, and movement in early embryosR35GM118146 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI STATHOPOULOS, ANGELIKE · 2016 to 2025
$5.8M
Regulation of long distance enhancer-promoter interactions by promoter-proximal elementsR01HD106799 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI Angelike Stathopoulos · 2022 to 2026
$1.8M
NICHD NIH HHS R01 HD106799NIGMS NIH HHS R35 GM118146U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) R01HD106799U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM118146
6 · The paper itself

Abstract

Chromatin conformation is thought to be critical for enhancer function, but its dynamic, nanoscale organization is difficult to measure directly. Here we introduce PLOTTED (Probabilistic Localization of Oligopaint Tagged Target Element Distances), an integrated imaging and computational framework that infers chromatin architecture from targeted high-resolution imaging of cis-regulatory modules (CRMs). PLOTTED generates spatial distance distributions between DNA loci, enabling quantitative modeling of chromatin configurations across developmental time, spatial axes, and genotypes. Applying PLOTTED to the brinker locus in Drosophila embryos, we measured distances among three CRMs and used chromatin geometry as a proxy for regulatory activity. In wild type, CRM configurations shift dynamically at nuclear cycle 13, whereas these changes are delayed in mutants and vary along the dorsal-ventral and anterior-posterior axes. Importantly, these conformational changes correlate with altered gene expression. Together, our findings position PLOTTED as a probabilistic, single-locus framework for interpreting chromatin architecture in development and disease.

Indexed as

ChromatinDNADrosophila melanogasterAnimalsDrosophilaDrosophila ProteinsEmbryo, NonmammalianGene Expression Regulation, DevelopmentalGenetic LociHomeodomain ProteinsRepressor ProteinsTrans-Activatorsbcd protein, DrosophilaChromatinDNADrosophila ProteinsHomeodomain ProteinsRepressor ProteinsTrans-Activators

Identifiers

PMID41540049
PMCPMC12914033

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.