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SSX2 is a novel DNA-binding protein that antagonizes polycomb group body formation and gene repression
Author(s) -
Morten F. Gjerstorff,
Mette Marie Relster,
Katrine Buch Vidén Greve,
Jesper B. Moeller,
Daniel Eliáš,
Jonas Lindgreen,
Steffen Schmidt,
Jan Mollenhauer,
Bjørn G. Voldborg,
Christina Bøg Pedersen,
Nadine Heidi Brückmann,
Niels Erik Møllegaard,
Henrik J. Ditzel
Publication year - 2014
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gku852
Subject(s) - biology , chromatin , polycomb group proteins , histone , histone h3 , chromatin remodeling , microbiology and biotechnology , ezh2 , regulation of gene expression , gene , gene expression , genetics , repressor
Polycomb group (PcG) complexes regulate cellular identity through epigenetic programming of chromatin. Here, we show that SSX2, a germline-specific protein ectopically expressed in melanoma and other types of human cancers, is a chromatin-associated protein that antagonizes BMI1 and EZH2 PcG body formation and derepresses PcG target genes. SSX2 further negatively regulates the level of the PcG-associated histone mark H3K27me3 in melanoma cells, and there is a clear inverse correlation between SSX2/3 expression and H3K27me3 in spermatogenesis. However, SSX2 does not affect the overall composition and stability of PcG complexes, and there is no direct concordance between SSX2 and BMI1/H3K27me3 presence at regulated genes. This suggests that SSX2 antagonizes PcG function through an indirect mechanism, such as modulation of chromatin structure. SSX2 binds double-stranded DNA in a sequence non-specific manner in agreement with the observed widespread association with chromatin. Our results implicate SSX2 in regulation of chromatin structure and function.

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