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Updated: Apr 19, 2026

Genome-wide Determination of Mammalian Replication Timing by DNA Content Measurement
Published on: January 19, 2017
Temporal separation of replication and transcription during S-phase progression
Matthieu Meryet-Figuiere1, Babak Alaei-Mahabadi, Mohamad Moustafa Ali
1a Department of Medical Genetics; Institute of Biomedicine; The Sahlgrenska Academy ; University of Gothenburg ; Gothenburg , Sweden.
This study reveals distinct temporal transcription patterns during S-phase, showing that gene transcription and DNA replication are separated in time. These findings offer new insights into cell cycle regulation.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- Cell cycle progression relies on precise transcriptional regulation during the S-phase.
- Understanding the dynamic interplay between DNA replication and gene expression is crucial for cell biology.
Purpose of the Study:
- To map the temporal patterns of transcriptional events occurring throughout the S-phase.
- To investigate the relationship between gene transcription timing and DNA replication timing during S-phase.
Main Methods:
- Utilized a nascent RNA capture assay combined with high-throughput sequencing.
- Analyzed temporal transcription patterns of S-phase-specific genes, including those for nucleosome assembly and DNA repair.
- Compared transcription timing with replication timing data.
Main Results:
- Identified distinct temporal transcription patterns for S-phase genes not apparent from total RNA levels.
- Observed that early replicating genes are transcribed later in S-phase, while late replicating genes are transcribed earlier.
- Found a global anti-correlation between replication and transcription timing when analyzing nascent RNA, but not total RNA.
Conclusions:
- Gene transcription and DNA replication are temporally separated during the S-phase of the cell cycle.
- Nascent RNA analysis provides a more accurate view of dynamic transcriptional events during S-phase than total RNA.
- These findings enhance our understanding of cell cycle regulation and gene expression dynamics.
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