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Updated: Jun 3, 2025

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts
Published on: January 2, 2018
Transcription factor networks in cellular quiescence
Mithun Mitra1,2, Sandra L Batista3, Hilary A Coller4,5,6
1Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, USA. mmitra@ucla.edu.
Mammalian cells enter a reversible quiescent state, pausing division but retaining proliferative potential. Transcription factors (TFs) control this quiescence, regulating gene expression and cell cycle arrest, with age-related dysregulation a key focus.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Mammalian tissues contain quiescent cells that can re-enter the cell cycle.
- Transcription factors (TFs) are crucial for maintaining quiescence by repressing proliferation genes.
- Understanding quiescence is vital for tissue repair and aging research.
Purpose of the Study:
- To review the role of transcription factors (TFs) in maintaining quiescent cell states.
- To discuss the dysregulation of TF networks in aging and cellular heterogeneity.
- To explore regulatory mechanisms of TFs at RNA, protein, and chromatin levels.
Main Methods:
- Literature review and synthesis of current research on quiescence and TFs.
- Discussion of findings from single-cell technologies.
- Analysis of gene regulatory networks in quiescent cells.
Main Results:
- Coordinated TF activities maintain reversible cell cycle arrest and protective signaling in quiescent cells.
- Age-related dysregulation of TF networks is an emerging area of study.
- Single-cell technologies reveal heterogeneity and complexity in quiescence TF networks.
Conclusions:
- Transcription factors are central to reversible quiescence and its age-related decline.
- Further research is needed to fully define TF networks in quiescent cells.
- Understanding TF regulation is key to manipulating quiescence for therapeutic benefit.
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