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JMJD3 intrinsically disordered region links the 3D-genome structure to TGFβ-dependent transcription activation

Author

Listed:
  • Marta Vicioso-Mantis

    (Consejo Superior de Investigaciones Científicas (CSIC))

  • Raquel Fueyo

    (Consejo Superior de Investigaciones Científicas (CSIC)
    Stanford University)

  • Claudia Navarro

    (Consejo Superior de Investigaciones Científicas (CSIC))

  • Sara Cruz-Molina

    (University of Cologne)

  • Wilfred F. J. Ijcken

    (Erasmus University Medical Center Rotterdam)

  • Elena Rebollo

    (Consejo Superior de Investigaciones Científicas (CSIC))

  • Álvaro Rada-Iglesias

    (University of Cologne
    CSIC/University of Cantabria)

  • Marian A. Martínez-Balbás

    (Consejo Superior de Investigaciones Científicas (CSIC))

Abstract

Enhancers are key regulatory elements that govern gene expression programs in response to developmental signals. However, how multiple enhancers arrange in the 3D-space to control the activation of a specific promoter remains unclear. To address this question, we exploited our previously characterized TGFβ-response model, the neural stem cells, focusing on a ~374 kb locus where enhancers abound. Our 4C-seq experiments reveal that the TGFβ pathway drives the assembly of an enhancer-cluster and precise gene activation. We discover that the TGFβ pathway coactivator JMJD3 is essential to maintain these structures. Using live-cell imaging techniques, we demonstrate that an intrinsically disordered region contained in JMJD3 is involved in the formation of phase-separated biomolecular condensates, which are found in the enhancer-cluster. Overall, in this work we uncover novel functions for the coactivator JMJD3, and we shed light on the relationships between the 3D-conformation of the chromatin and the TGFβ-driven response during mammalian neurogenesis.

Suggested Citation

  • Marta Vicioso-Mantis & Raquel Fueyo & Claudia Navarro & Sara Cruz-Molina & Wilfred F. J. Ijcken & Elena Rebollo & Álvaro Rada-Iglesias & Marian A. Martínez-Balbás, 2022. "JMJD3 intrinsically disordered region links the 3D-genome structure to TGFβ-dependent transcription activation," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30614-y
    DOI: 10.1038/s41467-022-30614-y
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    1. Karl Agger & Paul A. C. Cloos & Jesper Christensen & Diego Pasini & Simon Rose & Juri Rappsilber & Irina Issaeva & Eli Canaani & Anna Elisabetta Salcini & Kristian Helin, 2007. "UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development," Nature, Nature, vol. 449(7163), pages 731-734, October.
    2. Patrick Cramer, 2019. "Organization and regulation of gene transcription," Nature, Nature, vol. 573(7772), pages 45-54, September.
    3. Robert D. Phair & Tom Misteli, 2000. "High mobility of proteins in the mammalian cell nucleus," Nature, Nature, vol. 404(6778), pages 604-609, April.
    4. Bi Shi & Wei Li & Yansu Song & Zhenjia Wang & Rui Ju & Aleksandra Ulman & Jing Hu & Francesco Palomba & Yanfang Zhao & John Philip Le & William Jarrard & David Dimoff & Michelle A. Digman & Enrico Gra, 2021. "UTX condensation underlies its tumour-suppressive activity," Nature, Nature, vol. 597(7878), pages 726-731, September.
    5. Huasong Lu & Dan Yu & Anders S. Hansen & Sourav Ganguly & Rongdiao Liu & Alec Heckert & Xavier Darzacq & Qiang Zhou, 2018. "Phase-separation mechanism for C-terminal hyperphosphorylation of RNA polymerase II," Nature, Nature, vol. 558(7709), pages 318-323, June.
    6. Jill E. Moore & Michael J. Purcaro & Henry E. Pratt & Charles B. Epstein & Noam Shoresh & Jessika Adrian & Trupti Kawli & Carrie A. Davis & Alexander Dobin & Rajinder Kaul & Jessica Halow & Eric L. No, 2020. "Expanded encyclopaedias of DNA elements in the human and mouse genomes," Nature, Nature, vol. 583(7818), pages 699-710, July.
    7. Diana M. Mitrea & Jaclyn A. Cika & Christopher B. Stanley & Amanda Nourse & Paulo L. Onuchic & Priya R. Banerjee & Aaron H. Phillips & Cheon-Gil Park & Ashok A. Deniz & Richard W. Kriwacki, 2018. "Self-interaction of NPM1 modulates multiple mechanisms of liquid–liquid phase separation," Nature Communications, Nature, vol. 9(1), pages 1-13, December.
    8. Yang Eric Guo & John C. Manteiga & Jonathan E. Henninger & Benjamin R. Sabari & Alessandra Dall’Agnese & Nancy M. Hannett & Jan-Hendrik Spille & Lena K. Afeyan & Alicia V. Zamudio & Krishna Shrinivas , 2019. "Pol II phosphorylation regulates a switch between transcriptional and splicing condensates," Nature, Nature, vol. 572(7770), pages 543-548, August.
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