Details

Autor(en) / Beteiligte

• Pramio, Dimitrius Tansini
• Vieceli, Felipe Monteleone
• Varella-Branco, Elisa
• Goes, Carolina Purcell
• Kobayashi, Gerson Shigeru
• da Silva Pelegrina, Diogo Vieira
• de Moraes, Beatriz Caroline
• El Allam, Aicha
• De Kumar, Bony
• Jara, Gabriel
• Farfel, José Marcelo
• Bennett, David Alan
• Kundu, Somanath
• Viapiano, Mariano S.
• Reis, Eduardo Moraes
• de Oliveira, Paulo Sergio Lopes
• dos Santos e Passos-Bueno, Maria Rita
• Rothlin, Carla V.
• Ghosh, Sourav
• Schechtman, Deborah

Titel

DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ

Ist Teil von

• Biochimica et biophysica acta. Gene regulatory mechanisms, 2023-03, Vol.1866 (1), p.194909-194909, Article 194909

Ort / Verlag

Netherlands: Elsevier B.V

Erscheinungsjahr

2023

Quelle

Elsevier ScienceDirect

Beschreibungen/Notizen

• Protein kinase M zeta, PKMζ, is a brain enriched kinase with a well characterized role in Long-Term Potentiation (LTP), the activity-dependent strengthening of synapses involved in long-term memory formation. However, little is known about the molecular mechanisms that maintain the tissue specificity of this kinase. Here, we characterized the epigenetic factors, mainly DNA methylation, regulating PKMζ expression in the human brain. The PRKCZ gene has an upstream promoter regulating Protein kinase C ζ (PKCζ), and an internal promoter driving PKMζ expression. A demethylated region, including a canonical CREB binding site, situated at the internal promoter was only observed in human CNS tissues. The induction of site-specific hypermethylation of this region resulted in decreased CREB1 binding and downregulation of PKMζ expression. Noteworthy, CREB binding sites were absent in the upstream promoter of PRKCZ locus, suggesting a specific mechanism for regulating PKMζ expression. These observations were validated using a system of human neuronal differentiation from induced pluripotent stem cells (iPSCs). CREB1 binding at the internal promoter was detected only in differentiated neurons, where PKMζ is expressed. The same epigenetic mechanism in the context of CREB binding site was identified in other genes involved in neuronal differentiation and LTP. Additionally, aberrant DNA hypermethylation at the internal promoter was observed in cases of Alzheimer's disease, correlating with decreased expression of PKMζ in patient brains. Altogether, we present a conserved epigenetic mechanism regulating PKMζ expression and other genes enhanced in the CNS with possible implications in neuronal differentiation and Alzheimer's disease. [Display omitted] •DNA methylation, of a CRE regulates the specific expression of PKMζ in human brain.•CRE site methylation regulates brain-specific expression of Long-term potentiation genes.•PKMζ expression decreases and promoter methylation increases in Alzheimer’s disease.