The histone demethylase PHF8 regulates astrocyte differentiation and function

被引:9
|
作者
Iacobucci, Simona [1 ]
Padilla, Natalia [2 ]
Gabrielli, Martina [3 ]
Navarro, Claudia [1 ]
Lombardi, Marta [3 ]
Vicioso-Mantis, Marta [1 ]
Verderio, Claudia [3 ]
de la Cruz, Xavier [2 ]
Martinez-Balbas, Marian A. [1 ]
机构
[1] CSIC, Dept Mol Genom, Inst Biol Mol Barcelona IBMB, Barcelona 08028, Spain
[2] Vall dHebron Inst Res VHIR, Res Unit Clin & Translat Bioinformat, Passeig Vall dHebron 119, E-08035 Barcelona, Spain
[3] CNR, Inst Neurosci, Via Vanvitelli 32, I-20129 Milan, Italy
来源
DEVELOPMENT | 2021年 / 148卷 / 12期
关键词
PHF8; Histone demethylation; Chromatin transcription; Astrocyte differentiation; Synapse; XLID; LINKED MENTAL-RETARDATION; PLANT HOMEODOMAIN; NFIA CONTROLS; GENE; REVEALS; CELLS; ASTROGLIOGENESIS; PROGENITOR; MUTATIONS; PROTEINS;
D O I
10.1242/dev.194951
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Epigenetic factors have been shown to play a crucial role in X-linked intellectual disability (XLID). Here, we investigate the contribution of the XLID-associated histone demethylase PHF8 to astrocyte differentiation and function. Using genome-wide analyses and biochemical assays in mouse astrocytic cultures, we reveal a regulatory crosstalk between PHF8 and the Notch signaling pathway that balances the expression of the master astrocytic gene Nfia. Moreover, PHF8 regulates key synaptic genes in astrocytes by maintaining low levels of H4K20me3. Accordingly, astrocytic-PHF8 depletion has a striking effect on neuronal synapse formation and maturation in vitro. These data reveal that PHF8 is crucial in astrocyte development to maintain chromatin homeostasis and limit heterochromatin formation at synaptogenic genes. Our studies provide insights into the involvement of epigenetics in intellectual disability.
引用
收藏
页数:14
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