8vo0: Difference between revisions
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==H3K36me3-modified nucleosome bound to PRC2_AJ1-450 with histone H3 tail disengaged== | |||
<StructureSection load='8vo0' size='340' side='right'caption='[[8vo0]], [[Resolution|resolution]] 3.30Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8vo0]] is a 10 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Xenopus_laevis Xenopus laevis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8VO0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8VO0 FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.3Å</td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8vo0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8vo0 OCA], [https://pdbe.org/8vo0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8vo0 RCSB], [https://www.ebi.ac.uk/pdbsum/8vo0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8vo0 ProSAT]</span></td></tr> | |||
</table> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/H32_HUMAN H32_HUMAN] | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Polycomb repressive complex 2 (PRC2) trimethylates histone H3 on K27 (H3K27me3) leading to gene silencing that is essential for embryonic development and maintenance of cell identity. PRC2 is regulated by protein cofactors and their crosstalk with histone modifications. Trimethylated histone H3 on K4 (H3K4me3) and K36 (H3K36me3) localize to sites of active transcription and inhibit PRC2 activity through unknown mechanisms. Using cryo-electron microscopy, we reveal that histone H3 tails containing H3K36me3 engage poorly with PRC2 and preclude its effective interaction with chromatin, while H3K4me3 binds to the allosteric site in the EED subunit, acting as an antagonist that competes with activators required for spreading of the H3K27me3 repressive mark. Thus, the location of the H3K4me3 and H3K36me3 modifications along the H3 tail allows them to target two requirements for efficient trimethylation of H3K27 by PRC2. We further show that the JARID2 cofactor modulates PRC2 activity in the presence of these histone modifications. | |||
Structural basis for the inhibition of PRC2 by active transcription histone posttranslational modifications.,Cookis T, Lydecker A, Sauer P, Kasinath V, Nogales E Nat Struct Mol Biol. 2025 Jan 7. doi: 10.1038/s41594-024-01452-x. PMID:39774834<ref>PMID:39774834</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
[[Category: | </div> | ||
<div class="pdbe-citations 8vo0" style="background-color:#fffaf0;"></div> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Xenopus laevis]] | |||
[[Category: Cookis T]] | |||
[[Category: Nogales E]] | |||
Latest revision as of 13:12, 22 January 2025
H3K36me3-modified nucleosome bound to PRC2_AJ1-450 with histone H3 tail disengagedH3K36me3-modified nucleosome bound to PRC2_AJ1-450 with histone H3 tail disengaged
Structural highlights
FunctionPublication Abstract from PubMedPolycomb repressive complex 2 (PRC2) trimethylates histone H3 on K27 (H3K27me3) leading to gene silencing that is essential for embryonic development and maintenance of cell identity. PRC2 is regulated by protein cofactors and their crosstalk with histone modifications. Trimethylated histone H3 on K4 (H3K4me3) and K36 (H3K36me3) localize to sites of active transcription and inhibit PRC2 activity through unknown mechanisms. Using cryo-electron microscopy, we reveal that histone H3 tails containing H3K36me3 engage poorly with PRC2 and preclude its effective interaction with chromatin, while H3K4me3 binds to the allosteric site in the EED subunit, acting as an antagonist that competes with activators required for spreading of the H3K27me3 repressive mark. Thus, the location of the H3K4me3 and H3K36me3 modifications along the H3 tail allows them to target two requirements for efficient trimethylation of H3K27 by PRC2. We further show that the JARID2 cofactor modulates PRC2 activity in the presence of these histone modifications. Structural basis for the inhibition of PRC2 by active transcription histone posttranslational modifications.,Cookis T, Lydecker A, Sauer P, Kasinath V, Nogales E Nat Struct Mol Biol. 2025 Jan 7. doi: 10.1038/s41594-024-01452-x. PMID:39774834[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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