Author
Listed:
- Lennart Hilbert
(Center for Systems Biology Dresden
Max Planck Institute of Molecular Cell Biology and Genetics
Max Planck Institute for the Physics of Complex Systems
Karlsruhe Institute of Technology)
- Yuko Sato
(Tokyo Institute of Technology)
- Ksenia Kuznetsova
(Max Planck Institute of Molecular Cell Biology and Genetics)
- Tommaso Bianucci
(Max Planck Institute of Molecular Cell Biology and Genetics
Max Planck Institute for the Physics of Complex Systems)
- Hiroshi Kimura
(Tokyo Institute of Technology)
- Frank Jülicher
(Center for Systems Biology Dresden
Max Planck Institute for the Physics of Complex Systems
Technical University Dresden
Technical University Dresden)
- Alf Honigmann
(Max Planck Institute of Molecular Cell Biology and Genetics)
- Vasily Zaburdaev
(Center for Systems Biology Dresden
Max Planck Institute for the Physics of Complex Systems
Friedrich-Alexander Universität Erlangen-Nuremberg, Max Planck Zentrum für Physik und Medizin)
- Nadine L. Vastenhouw
(Max Planck Institute of Molecular Cell Biology and Genetics
University of Lausanne)
Abstract
In eukaryotes, DNA is packed inside the cell nucleus in the form of chromatin, which consists of DNA, proteins such as histones, and RNA. Euchromatin, which is permissive for transcription, is spatially organized into transcriptionally inactive domains interspersed with pockets of transcriptional activity. While transcription and RNA have been implicated in euchromatin organization, it remains unclear how their interplay forms and maintains transcription pockets. Here we combine theory and experiment to analyze the dynamics of euchromatin organization as pluripotent zebrafish cells exit mitosis and begin transcription. We show that accumulation of RNA induces formation of transcription pockets which displace transcriptionally inactive chromatin. We propose that the accumulating RNA recruits RNA-binding proteins that together tend to separate from transcriptionally inactive euchromatin. Full phase separation is prevented because RNA remains tethered to transcribed euchromatin through RNA polymerases. Instead, smaller scale microphases emerge that do not grow further and form the typical pattern of euchromatin organization.
Suggested Citation
Lennart Hilbert & Yuko Sato & Ksenia Kuznetsova & Tommaso Bianucci & Hiroshi Kimura & Frank Jülicher & Alf Honigmann & Vasily Zaburdaev & Nadine L. Vastenhouw, 2021.
"Transcription organizes euchromatin via microphase separation,"
Nature Communications, Nature, vol. 12(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21589-3
DOI: 10.1038/s41467-021-21589-3
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Citations
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Cited by:
- Hossein Salari & Geneviève Fourel & Daniel Jost, 2024.
"Transcription regulates the spatio-temporal dynamics of genes through micro-compartmentalization,"
Nature Communications, Nature, vol. 15(1), pages 1-15, December.
- Aayush Kant & Zixian Guo & Vinayak Vinayak & Maria Victoria Neguembor & Wing Shun Li & Vasundhara Agrawal & Emily Pujadas & Luay Almassalha & Vadim Backman & Melike Lakadamyali & Maria Pia Cosma & Viv, 2024.
"Active transcription and epigenetic reactions synergistically regulate meso-scale genomic organization,"
Nature Communications, Nature, vol. 15(1), pages 1-19, December.
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