JAZF1-SUZ12 dysregulates PRC2 function and gene expression during cell differentiation

Published: 20 April 2022| Version 1 | DOI: 10.17632/52rbsgb6by.1
Contributors:
Richard Jenner,
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Description

Polycomb repressive complex 2 (PRC2) methylates histone H3 lysine 27 (H3K27me3) to maintain gene repression and is essential for cell differentiation. In low-grade endometrial stromal sarcoma (LG-ESS), the PRC2 subunit SUZ12 is often fused with the NuA4/TIP60 subunit JAZF1. We show that JAZF1-SUZ12 dysregulates PRC2 composition, genome occupancy, histone modification, gene expression and cell differentiation. Loss of the SUZ12 N-terminus in the fusion protein abrogated interaction with specific PRC2 accessory factors, reduced occupancy at PRC2 target genes, and diminished H3K27me3. Fusion to JAZF1 increased H4Kac at PRC2 target genes and triggered recruitment to JAZF1 binding sites during cell differentiation. In human endometrial stromal cells, JAZF1-SUZ12 upregulated PRC2 target genes normally activated during decidualization while repressing genes associated with immune clearance, and JAZF1-SUZ12-induced genes were also overexpressed in LG-ESS. These results reveal defects in chromatin regulation, gene expression and cell differentiation caused by JAZF1-SUZ12, which may underlie its role in oncogenesis.

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Institutions

University College London

Categories

Biochemistry, Endometrial Cancer, Immunoprecipitation, Chromatin, Epigenetics

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