Polycomb protein binding and looping in the ON transcriptional state.

Sci Adv

Institute of Comparative Medicine, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.

Published: April 2024

AI Article Synopsis

  • Polycomb group (PcG) proteins play a crucial role in silencing developmental genes by modifying histones and compacting chromatin through two main complexes, PRC1 and PRC2, which are directed to DNA by specific regions known as CpG islands (CGIs) and Polycomb response elements (PREs).
  • When genes are turned OFF, PcG proteins attach to PREs, causing gene silencing through stabilizing loops that connect these elements.
  • Interestingly, while most PcG proteins detach from PREs when genes are active (ON state), a specific PRC1 component, Ph, stays bound, and PREs can create loops with each other and nearby enhancers, indicating their role as important structural features for regulating gene

Article Abstract

Polycomb group (PcG) proteins mediate epigenetic silencing of important developmental genes by modifying histones and compacting chromatin through two major protein complexes, PRC1 and PRC2. These complexes are recruited to DNA by CpG islands (CGIs) in mammals and Polycomb response elements (PREs) in . When PcG target genes are turned OFF, PcG proteins bind to PREs or CGIs, and PREs serve as anchors that loop together and stabilize gene silencing. Here, we address which PcG proteins bind to PREs and whether PREs mediate looping when their targets are in the ON transcriptional state. While the binding of most PcG proteins decreases at PREs in the ON state, one PRC1 component, Ph, remains bound. Further, PREs can loop to each other and with presumptive enhancers in the ON state and, like CGIs, may act as tethering elements between promoters and enhancers. Overall, our data suggest that PREs are important looping elements for developmental loci in both the ON and OFF states.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11042752PMC
http://dx.doi.org/10.1126/sciadv.adn1837DOI Listing

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