9YNZ

Human PU.1 ETS-Domain (165-270) Bound to d(5'-AATAAGCGGAAGTGGG-3') d(5'-TCCCACT*CPD*CGCTTAT-3')

Summary for 9YNZ

• Entry DOI: 10.2210/pdb9ynz/pdb
• Related: 9OA4 9OB0
• Descriptor: DNA (5'-D(*AP*AP*TP*AP*AP*GP*CP*GP*GP*AP*AP*GP*TP*GP*GP*G)-3'), DNA (5'-D(P*CP*CP*CP*AP*CP*T*(CPD)P*CP*GP*CP*TP*TP*AP*T)-3'), Transcription factor PU.1, ... (4 entities in total)
• Functional Keywords: transcription factor, protein-dna complex, ets family, ets, pu.1, transcription-dna complex, dna mismatch, transcription
• Biological source: Homo sapiens (human); More
• Total number of polymer chains: 3
• Total formula weight: 22247.98

Authors

Terrell, J.R.,Poon, G.M.K. (deposition date: 2025-10-13, release date: 2025-10-22, Last modification date: 2026-08-05)

Primary citation

Sivapragasam, S.,Terrell, J.R.,van der Vaart, A.,Germann, M.W.,Laughery, M.F.,Everly, M.E.,Adhikari, S.P.,Hrdlicka, P.J.,Wyrick, J.J.,Poon, G.M.K.
Molecular basis of UV lesion binding and repair inhibition by ETS-family transcription factors.
Nucleic Acids Res., 54:-, 2026

PubMed Abstract: Mutation hotspots in melanoma frequently occur at DNA binding sites of E26 transformation-specific (ETS)-family transcription factors, as ETS factors stimulate the formation of UV-induced cyclobutane pyrimidine dimers (CPDs) while suppressing repair at ETS-bound DNA sites. To elucidate the molecular mechanism by which ETS factors bind to damaged DNA sites and inhibit repair, we investigated the binding of members from the three major classes of the ETS superfamily (Ets1, ELF1, and PU.1) to cognate DNA containing a cis-syn TpT CPD. These site-specific CPDs modulated ETS recognition and repair by a model repair enzyme in a position-dependent manner. Specifically, a deaminated CPD located in a damage hotspot in the ETS binding motif consistently stimulated binding and inhibited T4 PDG (a CPD repair enzyme) by all three paralogs. Co-crystal structures of PU.1 reveal that CPDs and mismatches are recognized within the framework of canonical ETS/DNA complexes. Molecular dynamics simulations in explicit solvent show that CPD introduces compensatory structural dynamics to both the free and ETS-bound states that strongly modify the underlying thermodynamics of recognition. The results offer a molecular basis for how ETS factors induce mutation hotspots in skin cancers and other UV-exposed tissues by binding to CPD-containing sites and inhibiting their repair.

PubMed: 42500821
DOI: 10.1093/nar/gkag711

Experimental method

X-RAY DIFFRACTION (2.05 Å)