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Updated: Mar 11, 2026

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
Published on: September 20, 2018
Insight into the machinery that oils chromatin dynamics
Roni H G Wright1,2, Narcis Fernandez-Fuentes3, Baldomero Oliva2
1a Gene Regulation Stem Cells and Cancer Program, Center for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST) , Barcelona , Spain.
Cells utilize nuclear ATP synthesis for rapid chromatin reorganization during stress. This process, activated by hormones, uses ADP-ribose and pyrophosphate to fuel DNA accessibility and cell survival.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Chromatin packaging allows compact genetic information storage and selective DNA access.
- ATP-dependent chromatin remodelers use ATP hydrolysis for DNA accessibility.
- The source of ATP for nuclear chromatin remodeling is largely unexplored.
Purpose of the Study:
- Investigate the energetic cost of chromatin configuration changes.
- Explore nuclear ATP synthesis for chromatin remodeling during cellular reprogramming.
- Provide historical context, detailed enzymatic steps, and potential enzyme structure for nuclear ATP synthesis.
Main Methods:
- Investigated nuclear ATP synthesis mechanism.
- Identified ADP-ribose and pyrophosphate as substrates.
- Examined hormone-induced activation of nuclear ATP production.
Main Results:
- Discovered a nuclear ATP synthesis mechanism activated by hormones.
- This mechanism utilizes ADP-ribose and pyrophosphate.
- Suggests a dedicated nuclear energy production for rapid chromatin reorganization.
Conclusions:
- Nuclear ATP synthesis is activated in response to hormones.
- This pathway provides energy for rapid chromatin reorganization and cell survival.
- Highlights a novel link between nuclear energy metabolism and gene regulation.
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