Benchmarking three simple DNA staining-based image metrics for live-cell tracking of chromatin organization
- Journal
- Nucleus (Austin, Tex.) (Q1)
- Published
- 12 September 2026
- Study design
- Unclassified
- Evidence level
- Level 5, Expert Opinion (CEBM 5)
- Authors
- Minwoo Kang, Aidan Tomas Cabral, Manasi Sawant, Hawa Racine Thiam
- PMID
- 42730618
- DOI
- 10.1080/19491034.2026.2721777
Why clinicians should know about it
- Picked for Histology (paper of the day, 17 September 2026): DNA staining metrics track chromatin reorganization in live cells
Abstract
Quantifying chromatin-state dynamics in living cells remains challenging, in part because most methods require fixation or cell lysis. Here, we introduce two simple DNA image-derived metrics - Diffuse Signal Index (DSI)and 1-Gini - and benchmark them against the coefficient of variation (CV) as fixation-free readouts of chromatin reorganization. Leveraging the pronounced compact-to-decompact chromatin transition of NETosis, we show that all three metrics track progressive chromatin reorganization, with DSI providing the strongest trajectory-level discrimination between NETing and non-NETing cells. All three metrics also correlate with ATAC-see-based chromatin accessibility measurement in fixed cells, supporting their biological interpretability. In dividing cells, the metrics capture mitotic chromatin compaction and post-mitotic decompaction, demonstrating applicability in diverse biological processes. Together, these results provide a practical framework for extracting readouts of chromatin reorganization from routine live-cell DNA staining. We also provide NucMetrics, an open-source ImageJ/Fiji macro toolset for easily computing CV, DSI and 1-Gini.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.