# PRC2 Diversity in Neuronal Differentiation and Developmental Disorders

**Authors:** Jasmine Akoto, Thomas Roule, Naiara Akizu

PMC · DOI: 10.3390/genes16101191 · 2025-10-13

## TL;DR

This paper reviews how PRC2, an epigenetic complex, influences neuronal diversity and is linked to human developmental disorders.

## Contribution

The paper highlights recent discoveries on the evolutionary complexity of PRC2 subcomplexes and their role in neurodevelopment.

## Key findings

- PRC2 is crucial for epigenetic regulation in neuronal differentiation.
- Variations in PRC2 subcomplexes contribute to human developmental disorders.
- Evolutionary complexity of PRC2 is increasingly understood in neurodevelopmental contexts.

## Abstract

Advances in genetic studies have not only improved the diagnosis and treatment of neurodevelopmental disorders but also uncovered human-specific aspects of nervous system development. The generation of neuronal diversity in the human brain relies on tightly regulated epigenetic mechanisms, with Polycomb Repressive Complex 2 (PRC2) emerging as a key player. In this review, we first summarize foundational studies that established the role of PRC2 in the epigenetic maintenance of transcriptional silencing. We then highlight recent insights into the increasing evolutionary complexity of PRC2 subcomplexes, their roles in neurodevelopment, and their contribution to human developmental disorders.

## Linked entities

- **Proteins:** prc2 (protein regulator of cytokinesis 2)

## Full-text entities

- **Diseases:** Developmental Disorders (MESH:D002658)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12562812/full.md

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Source: https://tomesphere.com/paper/PMC12562812