Suppression of liquid–liquid phase separation by 1,6-hexanediol partially compromises the 3D genome organization in living cells

Author:

Ulianov Sergey V12ORCID,Velichko Artem K134,Magnitov Mikhail D135,Luzhin Artem V13,Golov Arkadiy K1,Ovsyannikova Natalia6,Kireev Igor I67,Gavrikov Alexey S8,Mishin Alexander S8,Garaev Azat K1ORCID,Tyakht Alexander V13ORCID,Gavrilov Alexey A13,Kantidze Omar L1ORCID,Razin Sergey V1ORCID

Affiliation:

1. Institute of Gene Biology Russian Academy of Science, 119334 Moscow, Russia

2. Faculty of Biology, Lomonosov Moscow State University, 119992 Moscow, Russia

3. Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology Russian Academy of Sciences, 119334 Moscow, Russia

4. Institute for Translational Medicine and Biotechnology, Sechenov First Moscow State Medical University, 119991 Moscow, Russia

5. Department of Biological and Medical Physics, Moscow Institute of Physics and Technology (National Research University), 141701 Dolgoprudny, Russia

6. A.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119992 Moscow, Russia

7. V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology, and Perinatology, 117997 Moscow, Russia

8. Shemyakin−Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russia

Abstract

Abstract Liquid–liquid phase separation (LLPS) contributes to the spatial and functional segregation of molecular processes within the cell nucleus. However, the role played by LLPS in chromatin folding in living cells remains unclear. Here, using stochastic optical reconstruction microscopy (STORM) and Hi-C techniques, we studied the effects of 1,6-hexanediol (1,6-HD)-mediated LLPS disruption/modulation on higher-order chromatin organization in living cells. We found that 1,6-HD treatment caused the enlargement of nucleosome clutches and their more uniform distribution in the nuclear space. At a megabase-scale, chromatin underwent moderate but irreversible perturbations that resulted in the partial mixing of A and B compartments. The removal of 1,6-HD from the culture medium did not allow chromatin to acquire initial configurations, and resulted in more compact repressed chromatin than in untreated cells. 1,6-HD treatment also weakened enhancer-promoter interactions and TAD insulation but did not considerably affect CTCF-dependent loops. Our results suggest that 1,6-HD-sensitive LLPS plays a limited role in chromatin spatial organization by constraining its folding patterns and facilitating compartmentalization at different levels.

Funder

Russian Science Foundation

Ministry of Science and Higher Education of the Russian Federation

Publisher

Oxford University Press (OUP)

Subject

Genetics

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