# Mechanism for controlled assembly of transcriptional condensates by Aire

**Authors:** Yu-San Huoh, Qianxia Zhang, Ricarda Törner, Sylvan C. Baca, Haribabu Arthanari, Sun Hur

PMC · DOI: 10.1038/s41590-024-01922-w · 2024-08-21

## TL;DR

This paper reveals how the Aire protein forms transcriptional condensates on enhancers to regulate gene expression, with a balance between different domains controlling its assembly.

## Contribution

The study identifies a multi-layered mechanism involving three Aire domains that regulate condensate assembly and transcriptional activity.

## Key findings

- Aire condensates assemble on enhancers and stimulate local transcriptional activity.
- The balance between PHD1 suppression and CTT stimulation is crucial for Aire condensate formation.
- Aire connects distant genomic loci through condensate assembly.

## Abstract

Transcriptional condensates play a crucial role in gene expression and regulation, yet their assembly mechanisms remain poorly understood. Here, we report a multi-layered mechanism for condensate assembly by autoimmune regulator (Aire), an essential transcriptional regulator that orchestrates gene expression reprogramming for central T cell tolerance. Aire condensates assemble on enhancers, stimulating local transcriptional activities and connecting disparate inter-chromosomal loci. This functional condensate formation hinges upon the coordination between three Aire domains: polymerization domain caspase activation recruitment domain (CARD), histone-binding domain (first plant homeodomain (PHD1)), and C-terminal tail (CTT). Specifically, CTT binds coactivators CBP/p300, recruiting Aire to CBP/p300-rich enhancers and promoting CARD-mediated condensate assembly. Conversely, PHD1 binds to the ubiquitous histone mark H3K4me0, keeping Aire dispersed throughout the genome until Aire nucleates on enhancers. Our findings showed that the balance between PHD1-mediated suppression and CTT-mediated stimulation of Aire polymerization is crucial to form transcriptionally active condensates at target sites, providing new insights into controlled polymerization of transcriptional regulators.

Sun Hur and colleagues examine the mechanism of Aire protein function underlying peripheral tissue antigen gene expression in thymic mTECs. They show that Aire condensates assemble on enhancers that are subject to intricate regulatory mechanisms, ensuring tight coordination of Aire CARD polymerization with genomic target recognition.

## Linked entities

- **Genes:** AIRE (autoimmune regulator) [NCBI Gene 326]
- **Proteins:** AIRE (autoimmune regulator), Crebbp (CREB binding protein)

## Full-text entities

- **Genes:** AIRE (autoimmune regulator) [NCBI Gene 326] {aka AIRE1, APECED, APS1, APSI, PGA1}, EGLN2 (egl-9 family hypoxia inducible factor 2) [NCBI Gene 112398] {aka EIT-6, EIT6, HIF-PH1, HIFPH1, HPH-1, HPH-3}

## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11362013/full.md

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Source: https://tomesphere.com/paper/PMC11362013