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PMID: 8221895 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

The crystal structure of the estrogen receptor DNA-binding domain bound to DNA: how receptors discriminate between their response elements.

Cell ·Vol. 75 ·No. 3 ·1993-11-05 ·Pages 567-78

Schwabe JW, Chapman L, Finch JT, Rhodes D

Abstract

The nuclear hormone receptors are a superfamily of ligand-activated DNA-binding transcription factors. We have determined the crystal structure (at 2.4 A) of the fully specific complex between the DNA-binding domain from the estrogen receptor and DNA. The protein binds as a symmetrical dimer to its palindromic binding site consisting of two 6 bp consensus half sites with three intervening base pairs. This structure reveals how the protein recognizes its own half site sequence rather than that of the related glucocorticoid receptor, which differs by only two base pairs. Since all nuclear hormone receptors recognize one or the other of these two consensus half site sequences, this recognition mechanism applies generally to the whole receptor family.

MeSH Terms
Amino Acid Sequence Base Composition Base Sequence Binding Sites Consensus Sequence Crystallography, X-Ray DNA/chemistry Gene Expression Regulation Hydrogen Bonding Macromolecular Substances Models, Molecular Molecular Sequence Data Protein Conformation Receptors, Estrogen/chemistry Receptors, Glucocorticoid/chemistry Regulatory Sequences, Nucleic Acid
Chemicals
Macromolecular Substances Receptors, Estrogen Receptors, Glucocorticoid DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Schwabe J W
Medical Research Council Laboratory of Molecular Biology, Cambridge, England.
Chapman L
Finch J T
Rhodes D
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1993-11-05
Pages
567-78
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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