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Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
Published on: December 10, 2012
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Replication timing uncovers a two-compartment nuclear architecture of interphase euchromatin
H S Akram1, E E Wear2, L Mickelson-Young2
1Department of Biological Science, Florida State University, Tallahassee, FL 32303, United States.
The Plant Cell
|February 20, 2026
Summary
Replication timing (RT) divides maize euchromatin into distinct spatial subcompartments. These early and middle S phase regions maintain separate nuclear territories, revealing a dynamic genome organization.
Area of Science:
- Genomics
- Cell Biology
- Epigenetics
Background:
- Replication timing (RT) regulates genome duplication during S phase.
- Previous models suggested maize euchromatin subcompartmentalization based on chromatin condensation and RT.
- The persistence of this compartmentalization throughout the cell cycle remained unclear.
Purpose of the Study:
- To investigate the spatial organization of maize euchromatin.
- To determine if proposed subcompartments persist throughout the cell cycle.
- To redefine the maize euchromatin 'A' compartment based on RT and spatial organization.
Main Methods:
- Genome-wide interaction data using Hi-C.
- Direct visualization of chromatin organization using 3D FISH painting.
- Analysis of epigenomic signatures associated with replication timing.
Main Results:
- Hi-C revealed distinct interaction patterns for early-S (negative insulation, long-range contacts) and middle-S regions.
- Early-S regions correlated strongly with open, transcriptionally active chromatin.
- 3D FISH confirmed early-S and middle-S regions occupy adjacent, non-overlapping nuclear sub-territories throughout interphase.
Conclusions:
- Maize euchromatin 'A' compartment comprises two spatially distinct subcompartments.
- These subcompartments are defined by high-frequency RT transitions along the genome.
- RT is a critical feature defining genome organization and has implications for chromatin-templated processes.
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