2a66: Difference between revisions

New page: left|200px<br /> <applet load="2a66" size="450" color="white" frame="true" align="right" spinBox="true" caption="2a66, resolution 2.20Å" /> '''Human Liver Recepto...
 
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<applet load="2a66" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2a66, resolution 2.20&Aring;" />
caption="2a66, resolution 2.20&Aring;" />
'''Human Liver Receptor Homologue DNA-Binding Domain (hLRH-1 DBD) in Complex with dsDNA from the hCYP7A1 Promoter'''<br />
'''Human Liver Receptor Homologue DNA-Binding Domain (hLRH-1 DBD) in Complex with dsDNA from the hCYP7A1 Promoter'''<br />


==Overview==
==Overview==
The DNA-binding and ligand-binding functions of nuclear receptors are, localized to independent domains separated by a flexible hinge. The, DNA-binding domain (DBD) of the human liver receptor homologue-1 (hLRH-1), which controls genes central to development and metabolic homeostasis, interacts with monomeric DNA response elements and contains an Ftz-F1, motif that is unique to the NR5A nuclear receptor subfamily. Here, we, present the 2.2A resolution crystal structure of the hLRH-1 DBD in complex, with duplex DNA, and elucidate the sequence-specific DNA contacts, essential for the ability of LRH-1 to bind to DNA as a monomer. We show, that the unique Ftz-F1 domain folds into a novel helix that packs against, the DBD but does not contact DNA. Mutations expected to disrupt the, positioning of the Ftz-F1 helix do not eliminate DNA binding but reduce, the transcriptional activity of full-length LRH-1 significantly. Moreover, we find that altering the Ftz-F1 helix positioning eliminates the, enhancement of LRH-1-mediated transcription by the coactivator GRIP1, an, action that is associated primarily with the distantly located, ligand-binding domain (LBD). Taken together, these results indicate that, subtle structural changes in a nuclear receptor DBD can exert long-range, functional effects on the LBD of a receptor, and significantly impact, transcriptional regulation.
The DNA-binding and ligand-binding functions of nuclear receptors are localized to independent domains separated by a flexible hinge. The DNA-binding domain (DBD) of the human liver receptor homologue-1 (hLRH-1), which controls genes central to development and metabolic homeostasis, interacts with monomeric DNA response elements and contains an Ftz-F1 motif that is unique to the NR5A nuclear receptor subfamily. Here, we present the 2.2A resolution crystal structure of the hLRH-1 DBD in complex with duplex DNA, and elucidate the sequence-specific DNA contacts essential for the ability of LRH-1 to bind to DNA as a monomer. We show that the unique Ftz-F1 domain folds into a novel helix that packs against the DBD but does not contact DNA. Mutations expected to disrupt the positioning of the Ftz-F1 helix do not eliminate DNA binding but reduce the transcriptional activity of full-length LRH-1 significantly. Moreover, we find that altering the Ftz-F1 helix positioning eliminates the enhancement of LRH-1-mediated transcription by the coactivator GRIP1, an action that is associated primarily with the distantly located ligand-binding domain (LBD). Taken together, these results indicate that subtle structural changes in a nuclear receptor DBD can exert long-range functional effects on the LBD of a receptor, and significantly impact transcriptional regulation.


==About this Structure==
==About this Structure==
2A66 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ZN and ACT as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2A66 OCA].  
2A66 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=ACT:'>ACT</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2A66 OCA].  


==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Hager, J.M.]]
[[Category: Hager, J M.]]
[[Category: McDonnell, D.P.]]
[[Category: McDonnell, D P.]]
[[Category: Ortlund, E.A.]]
[[Category: Ortlund, E A.]]
[[Category: Redinbo, M.R.]]
[[Category: Redinbo, M R.]]
[[Category: Safi, R.]]
[[Category: Safi, R.]]
[[Category: Solomon, I.H.]]
[[Category: Solomon, I H.]]
[[Category: ACT]]
[[Category: ACT]]
[[Category: ZN]]
[[Category: ZN]]
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[[Category: zinc finger]]
[[Category: zinc finger]]


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