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      Structure of the retinoid X receptor α-liver X receptor β (RXRα-LXRβ) heterodimer on DNA.

      Nature Structural & Molecular Biology

      Zinc Fingers, DNA, genetics, chemistry, Retinoid X Receptor alpha, Protein Structure, Tertiary, Protein Multimerization, Protein Binding, Promoter Regions, Genetic, Orphan Nuclear Receptors, Mutation, Models, Molecular, Ligands, Humans, metabolism, Escherichia coli, DNA, Complementary

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          Abstract

          Nuclear receptors (NRs) are conditional transcription factors with common multidomain organization that bind diverse DNA elements. How DNA sequences influence NR conformation is poorly understood. Here we report the crystal structure of the human retinoid X receptor α-liver X receptor β (RXRα-LXRβ) heterodimer on its cognate element, an AGGTCA direct repeat spaced by 4 nt. The complex has an extended X-shaped arrangement, with DNA- and ligand-binding domains crossed, in contrast to the parallel domain arrangement of other NRs that bind an AGGTCA direct repeat spaced by 1 nt. The LXRβ core binds DNA via canonical contacts and auxiliary DNA contacts that enhance affinity for the response element. Comparisons of RXRα-LXRβs in the crystal asymmetric unit and with previous NR structures reveal flexibility in NR organization and suggest a role for RXRα in adaptation of heterodimeric complexes to DNA.

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          Journal
          10.1038/nsmb.2778
          24561505

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