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5UQD

DPY-21 in complex with Fe(II) and alpha-Ketoglutarate

Summary for 5UQD
Entry DOI10.2210/pdb5uqd/pdb
DescriptorDumPY: shorter than wild-type, 2-OXOGLUTARIC ACID, FE (II) ION, ... (5 entities in total)
Functional Keywordsoxidoreductase, jmjc, h4k20me2 demethylase
Biological sourceCaenorhabditis elegans
Total number of polymer chains1
Total formula weight51074.01
Authors
Brejc, K.,Bian, Q.,Uzawa, S.,Wheeler, B.S.,Anderson, E.C.,King, D.S.,Kranzusch, P.J.,Preston, C.G.,Meyer, B.J. (deposition date: 2017-02-07, release date: 2017-09-13, Last modification date: 2024-03-06)
Primary citationBrejc, K.,Bian, Q.,Uzawa, S.,Wheeler, B.S.,Anderson, E.C.,King, D.S.,Kranzusch, P.J.,Preston, C.G.,Meyer, B.J.
Dynamic Control of X Chromosome Conformation and Repression by a Histone H4K20 Demethylase.
Cell, 171:85-102.e23, 2017
Cited by
PubMed Abstract: Chromatin modification and higher-order chromosome structure play key roles in gene regulation, but their functional interplay in controlling gene expression is elusive. We have discovered the machinery and mechanism underlying the dynamic enrichment of histone modification H4K20me1 on hermaphrodite X chromosomes during C. elegans dosage compensation and demonstrated H4K20me1's pivotal role in regulating higher-order chromosome structure and X-chromosome-wide gene expression. The structure and the activity of the dosage compensation complex (DCC) subunit DPY-21 define a Jumonji demethylase subfamily that converts H4K20me2 to H4K20me1 in worms and mammals. Selective inactivation of demethylase activity eliminates H4K20me1 enrichment in somatic cells, elevates X-linked gene expression, reduces X chromosome compaction, and disrupts X chromosome conformation by diminishing the formation of topologically associating domains (TADs). Unexpectedly, DPY-21 also associates with autosomes of germ cells in a DCC-independent manner to enrich H4K20me1 and trigger chromosome compaction. Our findings demonstrate the direct link between chromatin modification and higher-order chromosome structure in long-range regulation of gene expression.
PubMed: 28867287
DOI: 10.1016/j.cell.2017.07.041
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.798 Å)
Structure validation

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