# Regulation of Enhancers by SUMOylation Through TFAP2C Binding and Recruitment of HDAC Complex to the Chromatin

**Authors:** Tharindumala Abeywardana, Xiwei Wu, Shih-Ting Huang, Grace Aldana Masangkay, Andrei S. Rodin, Sergio Branciamore, Grigoriy Gogoshin, Arthur Li, Li Du, Neranjan Tharuka, Ross Tomaino, Yuan Chen

PMC · DOI: 10.21203/rs.3.rs-4201913/v1 · 2024-04-02

## TL;DR

This study shows how SUMOylation and the protein TFAP2C regulate enhancer activity by recruiting HDAC complexes to chromatin.

## Contribution

The study reveals a novel mechanism where SUMOylation and TFAP2C control enhancer marks through HDAC recruitment.

## Key findings

- SUMOylation regulates H3K27Ac at enhancers through UBA2 and TFAP2C.
- TFAP2C recruits HDAC complexes to chromatin, reducing H3K27Ac marks.
- SUMOylation of HDAC machinery proteins affects their recruitment to enhancers.

## Abstract

Enhancers are fundamental to gene regulation. Post-translational modifications by the small ubiquitin-like modifiers (SUMO) modify chromatin regulation enzymes, including histone acetylases and deacetylases. However, it remains unclear whether SUMOylation regulates enhancer marks, acetylation at the 27th lysine residue of the histone H3 protein (H3K27Ac). To investigate whether SUMOylation regulates H3K27Ac, we performed genome-wide ChIP-seq analyses and discovered that knockdown (KD) of the SUMO activating enzyme catalytic subunit UBA2 reduced H3K27Ac at most enhancers. Bioinformatic analysis revealed that TFAP2C-binding sites are enriched in enhancers whose H3K27Ac was reduced by UBA2 KD. ChIP-seq analysis in combination with molecular biological methods showed that TFAP2C binding to enhancers increased upon UBA2 KD or inhibition of SUMOylation by a small molecule SUMOylation inhibitor. However, this is not due to the SUMOylation of TFAP2C itself. Proteomics analysis of TFAP2C interactome on the chromatin identified histone deacetylation (HDAC) and RNA splicing machineries that contain many SUMOylation targets. TFAP2C KD reduced HDAC1 binding to chromatin and increased H3K27Ac marks at enhancer regions, suggesting that TFAP2C is important in recruiting HDAC machinery. Taken together, our findings provide insights into the regulation of enhancer marks by SUMOylation and TFAP2C and suggest that SUMOylation of proteins in the HDAC machinery regulates their recruitments to enhancers.

## Linked entities

- **Genes:** UBA2 (ubiquitin like modifier activating enzyme 2) [NCBI Gene 10054], TFAP2C (transcription factor AP-2 gamma) [NCBI Gene 7022], HDAC1 (histone deacetylase 1) [NCBI Gene 3065]
- **Proteins:** Sumo (Small ubiquitin like modifier), HDAC9 (histone deacetylase 9)

## Full-text entities

- **Genes:** TFAP2C (transcription factor AP-2 gamma) [NCBI Gene 7022] {aka AP2-GAMMA, ERF1, TFAP2G, hAP-2g}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}, UBA2 (ubiquitin like modifier activating enzyme 2) [NCBI Gene 10054] {aka ACCES, ARX, HRIHFB2115, SAE2}, HDAC1 (histone deacetylase 1) [NCBI Gene 3065] {aka GON-10, HD1, KDAC1, RPD3, RPD3L1}

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11030540/full.md

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Source: https://tomesphere.com/paper/PMC11030540