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PDBsum entry 6t90

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Top Page protein dna_rna ligands Protein-protein interface(s) links
Transcription PDB id
6t90
Contents
Protein chains
94 a.a.
82 a.a.
109 a.a.
93 a.a.
73 a.a.
74 a.a.
DNA/RNA
Ligands
PTD ×9

References listed in PDB file
Key reference
Title Mechanisms of oct4-Sox2 motif readout on nucleosomes.
Authors A.K.Michael, R.S.Grand, L.Isbel, S.Cavadini, Z.Kozicka, G.Kempf, R.D.Bunker, A.D.Schenk, A.Graff-Meyer, G.R.Pathare, J.Weiss, S.Matsumoto, L.Burger, D.Schübeler, N.H.Thomä.
Ref. Science, 2020, 368, 1460-1465. [DOI no: 10.1126/science.abb0074]
PubMed id 32327602
Abstract
Transcription factors (TFs) regulate gene expression through chromatin where nucleosomes restrict DNA access. To study how TFs bind nucleosome-occupied motifs, we focused on the reprogramming factors OCT4 and SOX2 in mouse embryonic stem cells. We determined TF engagement throughout a nucleosome at base-pair resolution in vitro, enabling structure determination by cryo-electron microscopy at two preferred positions. Depending on motif location, OCT4 and SOX2 differentially distort nucleosomal DNA. At one position, OCT4-SOX2 removes DNA from histone H2A and histone H3; however, at an inverted motif, the TFs only induce local DNA distortions. OCT4 uses one of its two DNA-binding domains to engage DNA in both structures, reading out a partial motif. These findings explain site-specific nucleosome engagement by the pluripotency factors OCT4 and SOX2, and they reveal how TFs distort nucleosomes to access chromatinized motifs.
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 Headers

 

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