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7ZEV

Free form of extended Cyp33-RRM

Summary for 7ZEV
Entry DOI10.2210/pdb7zev/pdb
Related7ZEW 7ZEX 7ZEY 7ZEZ
NMR InformationBMRB: 34724
DescriptorPeptidyl-prolyl cis-trans isomerase E (1 entity in total)
Functional Keywordsrrm, rna binding protein-structural protein complex, histone 3, h3k4me3, epigenetic, mll1 transcription regulation, infant leukemia, transcription
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight13189.85
Authors
Blatter, M.,Allain, F.,Meylan, C. (deposition date: 2022-03-31, release date: 2022-04-13, Last modification date: 2024-06-19)
Primary citationBlatter, M.,Meylan, C.,Clery, A.,Giambruno, R.,Nikolaev, Y.,Heidecker, M.,Solanki, J.A.,Diaz, M.O.,Gabellini, D.,Allain, F.H.
RNA binding induces an allosteric switch in Cyp33 to repress MLL1-mediated transcription.
Sci Adv, 9:eadf5330-eadf5330, 2023
Cited by
PubMed Abstract: Mixed-lineage leukemia 1 (MLL1) is a transcription activator of the HOX family, which binds to specific epigenetic marks on histone H3 through its third plant homeodomain (PHD3) domain. Through an unknown mechanism, MLL1 activity is repressed by cyclophilin 33 (Cyp33), which binds to MLL1 PHD3. We determined solution structures of Cyp33 RNA recognition motif (RRM) free, bound to RNA, to MLL1 PHD3, and to both MLL1 and the histone H3 lysine N6-trimethylated. We found that a conserved α helix, amino-terminal to the RRM domain, adopts three different positions facilitating a cascade of binding events. These conformational changes are triggered by Cyp33 RNA binding and ultimately lead to MLL1 release from the histone mark. Together, our mechanistic findings rationalize how Cyp33 binding to MLL1 can switch chromatin to a transcriptional repressive state triggered by RNA binding as a negative feedback loop.
PubMed: 37075125
DOI: 10.1126/sciadv.adf5330
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

227111

數據於2024-11-06公開中

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