6VIL
Crystal structure of mouse BAHCC1 BAH domain in complex with H3K27me3
Summary for 6VIL
Entry DOI | 10.2210/pdb6vil/pdb |
Descriptor | BAH and coiled-coil domain-containing protein 1, Histone H3.1 (2 entities in total) |
Functional Keywords | structural protein |
Biological source | Mus musculus (Mouse) More |
Total number of polymer chains | 12 |
Total formula weight | 154155.88 |
Authors | |
Primary citation | Fan, H.,Lu, J.,Guo, Y.,Li, D.,Zhang, Z.M.,Tsai, Y.H.,Pi, W.C.,Ahn, J.H.,Gong, W.,Xiang, Y.,Allison, D.F.,Geng, H.,He, S.,Diao, Y.,Chen, W.Y.,Strahl, B.D.,Cai, L.,Song, J.,Wang, G.G. BAHCC1 binds H3K27me3 via a conserved BAH module to mediate gene silencing and oncogenesis. Nat.Genet., 52:1384-1396, 2020 Cited by PubMed Abstract: Trimethylated histone H3 lysine 27 (H3K27me3) regulates gene repression, cell-fate determination and differentiation. We report that a conserved bromo-adjacent homology (BAH) module of BAHCC1 (BAHCC1) 'recognizes' H3K27me3 specifically and enforces silencing of H3K27me3-demarcated genes in mammalian cells. Biochemical, structural and integrated chromatin immunoprecipitation-sequencing-based analyses demonstrate that direct readout of H3K27me3 by BAHCC1 is achieved through a hydrophobic trimethyl-L-lysine-binding 'cage' formed by BAHCC1, mediating colocalization of BAHCC1 and H3K27me3-marked genes. BAHCC1 is highly expressed in human acute leukemia and interacts with transcriptional corepressors. In leukemia, depletion of BAHCC1, or disruption of the BAHCC1-H3K27me3 interaction, causes derepression of H3K27me3-targeted genes that are involved in tumor suppression and cell differentiation, leading to suppression of oncogenesis. In mice, introduction of a germline mutation at Bahcc1 to disrupt its H3K27me3 engagement causes partial postnatal lethality, supporting a role in development. This study identifies an H3K27me3-directed transduction pathway in mammals that relies on a conserved BAH 'reader'. PubMed: 33139953DOI: 10.1038/s41588-020-00729-3 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.301 Å) |
Structure validation
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