Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

9RTN

State 2 MAP 2 SPT6 with SETD2

Summary for 9RTN
Entry DOI10.2210/pdb9rtn/pdb
Related9GW2
EMDB information54247
DescriptorRNA polymerase II subunit D, DNA-directed RNA polymerase II subunit RPB7, Histone-lysine N-methyltransferase SETD2, ... (5 entities in total)
Functional Keywordsrna pol ii activated elongation complex co-transcriptional h3k36me3 setd2, transcription
Biological sourceHomo sapiens (human)
More
Total number of polymer chains5
Total formula weight484281.31
Authors
Walshe, J.L.,Ochmann, M.,Dienemann, C.,Cramer, P. (deposition date: 2025-07-03, release date: 2025-09-24, Last modification date: 2025-11-12)
Primary citationWalshe, J.L.,Ochmann, M.,Neef, U.,Dybkov, O.,Dienemann, C.,Oberthur, C.,Zheenbekova, A.,Urlaub, H.,Cramer, P.
Molecular mechanism of co-transcriptional H3K36 methylation by SETD2.
Nat Commun, 16:9565-9565, 2025
Cited by
PubMed Abstract: H3K36me3 is a hallmark of actively and recently transcribed genes and contributes to cellular memory and identity. The deposition of H3K36me3 occurs co-transcriptionally when the methyltransferase SETD2 associates with RNA polymerase II. Here we present three cryo-EM structures of SETD2 bound to RNA polymerase II elongation complexes at different states of nucleosome passage. Together with functional probing, our results suggest a 3-step mechanism of transcription-coupled H3K36me3 deposition. First, binding to the elongation factor SPT6 tethers the catalytic SET domain in proximity to the upstream DNA. Second, RNA polymerase II nucleosome passage leads to the transfer of a hexasome from downstream to upstream, poised for methylation. Finally, continued transcription leads to upstream nucleosome reassembly, partial dissociation of the histone chaperone FACT and sequential methylation of both H3 tails, completing H3K36me3 deposition of an upstream nucleosome after RNA polymerase II passage.
PubMed: 41162378
DOI: 10.1038/s41467-025-65439-y
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.82 Å)
Structure validation

246905

PDB entries from 2025-12-31

PDB statisticsPDBj update infoContact PDBjnumon