The histone demethylase PHF8 regulates astrocyte differentiation and function

Author:

Iacobucci Simona1,Padilla Natalia2,Gabrielli Martina3ORCID,Navarro Claudia1,Lombardi Marta3,Vicioso-Mantis Marta1ORCID,Verderio Claudia3,de la Cruz Xavier2,Martínez-Balbás Marian A.1ORCID

Affiliation:

1. Department of Molecular Genomics, Instituto de Biología Molecular de Barcelona (IBMB), Consejo Superior de Investigaciones Científicas (CSIC), Barcelona 08028, Spain

2. Research Unit in Clinical and Translational Bioinformatics, Vall d'Hebron Institute of Research (VHIR), Passeig de la Vall d'Hebron, 119; E-08035 Barcelona, Spain. Institut Català per la Recerca i Estudis Avançats (ICREA), Barcelona 08018, Spain

3. CNR Institute of Neuroscience, via Vanvitelli 32, 20129 Milan, Italy

Abstract

ABSTRACT 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.

Funder

Ministry of Economy

Ministerio de Economía, Industria y Competitividad, Gobierno de España

Boehringer Ingelheim

Ministerio de Ciencia e Innovación de España

Consejo Superior de Investigaciones Científicas

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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