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Updated: Jan 18, 2026

Combined Immunofluorescence and DNA FISH on 3D-preserved Interphase Nuclei to Study Changes in 3D Nuclear Organization
Published on: February 3, 2013
Inferring chromatin architecture at a single locus through probabilistic in situ DNA localization
Minh Tam Le1, James McGehee1, Leslie Dunipace1
1Division of Biology and Biological Engineering, California Institute of Technology, 1200 East California Blvd, Pasadena, CA, USA.
None:
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.
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