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Solution Structures of PPAR?2/RXR? Complexes.

ABSTRACT: PPAR? is a key regulator of glucose homeostasis and insulin sensitization. PPAR? must heterodimerize with its dimeric partner, the retinoid X receptor (RXR), to bind DNA and associated coactivators such as p160 family members or PGC-1? to regulate gene networks. To understand how coactivators are recognized by the functional heterodimer PPAR?/RXR? and to determine the topological organization of the complexes, we performed a structural study using small angle X-ray scattering of PPAR?/RXR? in complex with DNA from regulated gene and the TIF2 receptor interacting domain (RID). The solution structures reveal an asymmetry of the overall structure due to the crucial role of the DNA in positioning the heterodimer and indicate asymmetrical binding of TIF2 to the heterodimer.

SUBMITTER: Osz J

PROVIDER: S-EPMC3539437 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

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Solution Structures of PPARγ2/RXRα Complexes.

Osz Judit J Pethoukhov Maxim V MV Sirigu Serena S Svergun Dmitri I DI Moras Dino D Rochel Natacha N

PPAR research 20121218

PPARγ is a key regulator of glucose homeostasis and insulin sensitization. PPARγ must heterodimerize with its dimeric partner, the retinoid X receptor (RXR), to bind DNA and associated coactivators such as p160 family members or PGC-1α to regulate gene networks. To understand how coactivators are recognized by the functional heterodimer PPARγ/RXRα and to determine the topological organization of the complexes, we performed a structural study using small angle X-ray scattering of PPARγ/RXRα in co ...[more]

PMID: 23319938

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