Multimodal interactions drive chromatin phase separation and compaction

Author:

Ukmar-Godec Tina1ORCID,Cima-Omori Maria-Sol1ORCID,Yerkesh Zhadyra2,Eswara Karthik2ORCID,Yu Taekyung1ORCID,Ramesh Reshma1,Riviere Gwladys1,Ibanez de Opakua Alain1,Fischle Wolfgang2ORCID,Zweckstetter Markus13ORCID

Affiliation:

1. German Center for Neurodegenerative Diseases, Translational Structural Biology, Göttingen 37075, Germany

2. Bioscience Program, Biological and Environmental Science and Engineering Division, Laboratory of Chromatin Biochemistry, King Abdullah University of Science and Technology, Thuwal 23955, Saudi Arabia

3. Department of NMR-based Structural Biology, Max Planck Institute for Multidisciplinary Sciences, Göttingen 37077, Germany

Abstract

Gene silencing is intimately connected to DNA condensation and the formation of transcriptionally inactive heterochromatin by Heterochromatin Protein 1α (HP1α). Because heterochromatin foci are dynamic and HP1α can promote liquid–liquid phase separation, HP1α-mediated phase separation has been proposed as a mechanism of chromatin compaction. The molecular basis of HP1α-driven phase separation and chromatin compaction and the associated regulation by trimethylation of lysine 9 in histone 3 (H3K9me3), which is the hallmark of constitutive heterochromatin, is however largely unknown. Using a combination of chromatin compaction and phase separation assays, site-directed mutagenesis, and NMR-based interaction analysis, we show that human HP1α can compact chromatin in the absence of liquid–liquid phase separation. We further demonstrate that H3K9-trimethylation promotes compaction of chromatin arrays through multimodal interactions. The results provide molecular insights into HP1α-mediated chromatin compaction and thus into the role of human HP1α in the regulation of gene silencing.

Funder

EC | ERC | HORIZON EUROPE European Research Council

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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