image: (Left) In normal dentate gyrus, EED binds to EZH2, SUZ12 and RbAP46/48 to form an interactive PRC2 complex which regulates neurogenesis in the dentate gyrus. (Right) inactivation of EED leads to a remarkable malformation of the dentate gyrus. view more
Credit: Liu Changmei
The dentate gyrus (DG) is the input region of the hippocampus and plays an important role in learning and memory. Although emerging evidence suggested that abnormal expression of the polycomb repressive complex 2 protein (PRC2) might cause neurological disease, the underlying molecular mechanisms had not been explored until recently.
Now, in a study published in Stem Cell Reports, a team led by Prof. LIU Changmei from the State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology of the Chinese Academy of Sciences, has shown that the PcG protein EED is essential for the proper formation of the DG.
By generating an EED conditional knockout mouse model, the researchers found that disruption of EED resulted in postnatal lethality, impaired migration of granule cells, loss of the subgranular zone (SGZ), and a severely disrupted secondary radial glial scaffold in the hippocampus.
They then identified Ink4a/Arf (Cdkn2a) and Sox11 as key downstream targets of EED with distinct functions in modulating the proliferation and differentiation of neural stem/progenitor cells (NSPCs) in the DG.
They also for the first time provided functional and molecular evidence supporting the essential role of EED-mediated H3K27 methylation in the reorganization of NSPCs during DG development.
This study establishes EED as an important modulator of hippocampal development and provides novel mechanistic insights into the complex role that EED plays in brain development and neurological diseases.
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The research was supported by the Strategic Priority Research Program of the Chinese Academy of Sciences, the National Key Research and Development Program of China and the National Science Foundation of China.
Journal
Stem Cell Reports