Highly enriched BEND3 prevents the premature activation of bivalent genes during differentiation

Bivalent genes are ready for activation upon the arrival of developmental cues. Here, we report that BEND3 is a CpG island (CGI)-binding protein that is enriched at regulatory elements. The cocrystal structure of BEND3 in complex with its target DNA reveals the structural basis for its DNA methylation-sensitive binding property. Mouse embryos ablated of Bend3 died at the pregastrulation stage. Bend3 null embryonic stem cells (ESCs) exhibited severe defects in differentiation, during which hundreds of CGI-containing bivalent genes were prematurely activated. BEND3 is required for the stable association of polycomb repressive complex 2 (PRC2) at bivalent genes that are highly occupied by BEND3, which suggests a reining function of BEND3 in maintaining high levels of H3K27me3 at these bivalent genes in ESCs to prevent their premature activation in the forthcoming developmental stage.

Automated summary

BEND3 is a CpG island-binding protein that is enriched at regulatory elements. It binds to DNA in a methylation-sensitive manner. Mice embryos lacking Bend3 die at the pregastrulation stage, while Bend3 null embryonic stem cells exhibit severe defects in differentiation, leading to premature activation of hundreds of CpG island-containing bivalent genes. BEND3 is required for maintaining high levels of H3K27me3 at these bivalent genes in order to prevent their premature activation in upcoming developmental stages.