Abstract
Transcription in eukaryotes is regulated by chromatin-based mechanisms that control nucleosome occupancy, chromatin modifications, and transcription factor binding. We have previously shown that the transcription factor ADNP forms the ChAHP complex with the chromatin remodeler CHD4 and HP1 proteins, acting as a site-specific regulator of transcription and an antagonist of CTCF binding. However, the molecular basis of these functions remained unclear. Here, we demonstrate in mouse embryonic stem cells that the CHD4 subunit is essential for antagonizing CTCF and silencing the transcription of transposons, whereas HP1 proteins are dispensable. Although the remodeling activity of CHD4 is not required for ChAHP chromatin association, it is critical for both transposon repression and CTCF antagonism. Our findings support a model in which ADNP recruits chromatin-remodeling activity in a sequence-specific manner, enabling transcriptional control and local modulation of chromatin architecture.
| Original language | English |
|---|---|
| Pages (from-to) | 2754-2769.e9 |
| Journal | Molecular Cell |
| Volume | 86 |
| Issue number | 14 |
| Early online date | 7 Jul 2026 |
| DOIs | |
| Publication status | Published - 16 Jul 2026 |
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