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Updated: Aug 10, 2026

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
Published on: June 6, 2017
DRTF1/E2F: an expanding family of heterodimeric transcription factors implicated in cell-cycle control
1Laboratory of Eukaryotic Molecular Genetics, MRC National Institute for Medical Research, London, UK.
Abstract:
During the cell cycle, the transcription of certain genes is integrated with cell-cycle progression, thus providing an important level of control. In mammalian cells, DRTF1/E2F is a transcription activity comprising a group of related heterodimeric transcription factors that function in this integration process. The primary molecules involved in generating the afferent signals that converge on DRTF1/E2F belong to a class of proteins, exemplified by the retinoblastoma tumour suppressor gene product, whose activities are, in turn, regulated by cyclin-dependent kinases. The transcriptional activity of DRTF1/E2F is therefore regulated through a pathway that links the machinery of the cell cycle to the transcription apparatus. As such, it is likely to play a pivotal role in regulating cell-cycle progression.
Insights
Gene transcription is controlled during the cell cycle. In mammalian cells, the DRTF1/E2F transcription factor integrates cell-cycle progression signals, linking cell-cycle machinery to transcription.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- Cell-cycle progression involves regulated gene transcription for precise control.
- Transcription factors play a crucial role in integrating cellular processes.
- The retinoblastoma tumor suppressor protein is a key regulator in cell cycle control.
Purpose of the Study:
- To elucidate the role of DRTF1/E2F transcription factors in mammalian cell cycle regulation.
- To understand how extracellular signals are integrated with the cell cycle machinery.
- To investigate the pathway linking cell cycle regulators to transcriptional control.
Main Methods:
- Analysis of transcription factor activity in mammalian cell lines.
- Investigating the interaction between cell cycle proteins and transcription factors.
- Studying the regulation of DRTF1/E2F by cyclin-dependent kinases.
Main Results:
- DRTF1/E2F is identified as a key transcription activity integrating cell-cycle progression.
- Proteins like the retinoblastoma tumor suppressor gene product generate signals converging on DRTF1/E2F.
- Cyclin-dependent kinases regulate the activity of these signaling proteins.
Conclusions:
- DRTF1/E2F acts as a crucial link between cell cycle machinery and the transcription apparatus.
- This regulatory pathway is pivotal for controlling cell-cycle progression in mammalian cells.
- Understanding this mechanism provides insights into cell proliferation and tumor suppression.
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