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Highly conserved ENY2/Sus1 protein binds to Drosophila CTCF and is required for barrier activity.


ABSTRACT: Chromatin insulators affect interactions between promoters and enhancers/silencers and function as barriers for the spreading of repressive chromatin. Drosophila insulator protein dCTCF marks active promoters and boundaries of many histone H3K27 trimethylation domains associated with repressed chromatin. In particular, dCTCF binds to such boundaries between the parasegment-specific regulatory domains of the Bithorax complex. Here we demonstrate that the evolutionarily conserved protein ENY2 is recruited to the zinc-finger domain of dCTCF and is required for the barrier activity of dCTCF-dependent insulators in transgenic lines. Inactivation of ENY2 by RNAi in BG3 cells leads to the spreading of H3K27 trimethylation and Pc protein at several dCTCF boundaries. The results suggest that evolutionarily conserved ENY2 is responsible for barrier activity mediated by the dCTCF protein.

SUBMITTER: Maksimenko O 

PROVIDER: S-EPMC4169018 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature

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Highly conserved ENY2/Sus1 protein binds to Drosophila CTCF and is required for barrier activity.

Maksimenko Oksana O   Kyrchanova Olga O   Bonchuk Artem A   Stakhov Viacheslav V   Parshikov Alexander A   Georgiev Pavel P  

Epigenetics 20140801 9


Chromatin insulators affect interactions between promoters and enhancers/silencers and function as barriers for the spreading of repressive chromatin. Drosophila insulator protein dCTCF marks active promoters and boundaries of many histone H3K27 trimethylation domains associated with repressed chromatin. In particular, dCTCF binds to such boundaries between the parasegment-specific regulatory domains of the Bithorax complex. Here we demonstrate that the evolutionarily conserved protein ENY2 is r  ...[more]

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