1cs3

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1cs3, resolution 2.00Å

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STRUCTURE OF BTB/POZ TRANSCRIPTION REPRESSION DOMAIN FROM PROMELOCYTIC LEUKEMIA ZINC FINGER ONCOPROTEIN

Contents

Overview

The evolutionarily conserved BTB/POZ domain from the promyelocytic, leukemia zinc finger (PLZF) oncoprotein mediates transcriptional, repression through the recruitment of corepressor proteins containing, histone deacetylases in acute promyelocytic leukemia. We have determined, the 2.0 A crystal structure of the BTB/POZ domain from PLZF, (PLZF-BTB/POZ), and have carried out biochemical analysis of PLZF-BTB/POZ, harboring site-directed mutations to probe structure-function, relationships. The structure reveals a novel alpha/beta homodimeric fold, in which dimer interactions occur along two surfaces of the protein, subunits. The conservation of BTB/POZ domain residues at the core of the, protomers and at the dimer interface implies an analogous fold and, dimerization mode for BTB/POZ domains from otherwise functionally, unrelated proteins. Unexpectedly, the BTB/POZ domain forms dimer-dimer, interactions in the crystals, suggesting a mode for higher-order protein, oligomerization for BTB/POZ-mediated transcriptional repression., Biochemical characterization of PLZF-BTB/POZ harboring mutations in, conserved residues involved in protein dimerization reveals that the, integrity of the dimer interface is exquisitely sensitive to mutation and, that dimer formation is required for wild-type levels of transcriptional, repression. Interestingly, similar mutational analysis of residues within, a pronounced protein cleft along the dimer interface, which had been, implicated previously for interaction with corepressors, has negligible, effects on dimerization or transcriptional repression. Together, these, studies form a structure-function framework for understanding, BTB/POZ-mediated oligomerization and transcriptional repression, properties.

Disease

Known diseases associated with this structure: Leukemia, acute promyelocytic, PL2F/RARA type OMIM:[176797]

About this Structure

1CS3 is a Single protein structure of sequence from Homo sapiens with MG and GOL as ligands. Full crystallographic information is available from OCA.

Reference

Structure-function studies of the BTB/POZ transcriptional repression domain from the promyelocytic leukemia zinc finger oncoprotein., Li X, Peng H, Schultz DC, Lopez-Guisa JM, Rauscher FJ 3rd, Marmorstein R, Cancer Res. 1999 Oct 15;59(20):5275-82. PMID:10537309

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