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PDBsum entry 4x3e

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protein ligands links
Transcription PDB id
4x3e

 

 

 

 

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Contents
Protein chain
359 a.a.
Ligands
ALA-GLN-ARG-M3L-
PHE-ALA-GLN-SER
Waters ×175
PDB id:
4x3e
Name: Transcription
Title: Crystal structure of eed in complex with a trimethylated jarid2 peptide
Structure: Polycomb protein eed. Chain: a. Fragment: unp residues 77-441. Synonym: heed,wd protein associating with integrin cytoplasmic tails 1,wait-1. Engineered: yes. Ala-gln-arg-m3l-phe-ala-gln-ser. Chain: b. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: eed. Expressed in: escherichia coli. Expression_system_taxid: 562. Expressed in: synthetic construct. Expression_system_taxid: 32630
Resolution:
2.30Å     R-factor:   0.174     R-free:   0.224
Authors: N.Justin,S.J.Gamblin,R.Margueron
Key ref: S.Sanulli et al. (2015). Jarid2 Methylation via the PRC2 Complex Regulates H3K27me3 Deposition during Cell Differentiation. Mol Cell, 57, 769-783. PubMed id: 25620564 DOI: 10.1016/j.molcel.2014.12.020
Date:
28-Nov-14     Release date:   21-Jan-15    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
O75530  (EED_HUMAN) -  Polycomb protein EED from Homo sapiens
Seq:
Struc:
441 a.a.
359 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 

 
DOI no: 10.1016/j.molcel.2014.12.020 Mol Cell 57:769-783 (2015)
PubMed id: 25620564  
 
 
Jarid2 Methylation via the PRC2 Complex Regulates H3K27me3 Deposition during Cell Differentiation.
S.Sanulli, N.Justin, A.Teissandier, K.Ancelin, M.Portoso, M.Caron, A.Michaud, B.Lombard, S.T.da Rocha, J.Offer, D.Loew, N.Servant, M.Wassef, F.Burlina, S.J.Gamblin, E.Heard, R.Margueron.
 
  ABSTRACT  
 
Polycomb Group (PcG) proteins maintain transcriptional repression throughout development, mostly by regulating chromatin structure. Polycomb Repressive Complex 2 (PRC2), a component of the Polycomb machinery, is responsible for the methylation of histone H3 lysine 27 (H3K27me2/3). Jarid2 was previously identified as a cofactor of PRC2, regulating PRC2 targeting to chromatin and its enzymatic activity. Deletion of Jarid2 leads to impaired orchestration of gene expression during cell lineage commitment. Here, we reveal an unexpected crosstalk between Jarid2 and PRC2, with Jarid2 being methylated by PRC2. This modification is recognized by the Eed core component of PRC2 and triggers an allosteric activation of PRC2's enzymatic activity. We show that Jarid2 methylation is important to promote PRC2 activity at a locus devoid of H3K27me3 and for the correct deposition of this mark during cell differentiation. Our results uncover a regulation loop where Jarid2 methylation fine-tunes PRC2 activity depending on the chromatin context.
 

 

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