Abstract
The HMG-box protein capicua (CIC) is a conserved transcriptional repressor with key functions in development and disease. CIC binding of DNA requires both its HMG-box and a separate domain called C1. How these domains cooperate to recognize specific DNA sequences is not known. Here, we report the crystal structure of the human CIC HMG-box and C1 domains complexed with a DNA oligomer containing a consensus octameric binding site. We find that both domains adopt tri-helical structures that pack against opposite sides of the DNA helix. The C1 domain folds into a helix-turn-helix (HTH) structure, inserting into the DNA major groove to enhance affinity. We investigate the system using molecular dynamics simulations and binding assays that interrogate the observed HMG-box and C1 domain interface and prominent cancer variants. Our results reveal a unique bipartite DNA-binding module and provide insights into the effects of cancer and domain interface mutations.
| Original language | English |
|---|---|
| Journal | Structure |
| DOIs | |
| State | Accepted/In press - 2025 |
ASJC Scopus Subject Areas
- Structural Biology
- Molecular Biology
Keywords
- cancer mutations
- CIC
- DNA binding affinity
- EMSA
- helix-turn-helix
- HTH
- MST
- protein-DNA complex
- repressor protein
- Xray crystallography
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