Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.506959
Title: Characterisation of a novel nuclear receptor-like protein
Author: Granger, David William
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2009
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Abstract:
A genome threading algorithm was employed by Inpharmatica to identify a number of proteins with a predicted structure similar to that of the ligand binding domain (LBD) of nuclear receptors (NRs), an approach that has been successfully used to annotate the yeast transcription factor Oaf1 (Phelps et al, 2006). This work focuses on one such protein termed NR3, which is identical to TRPC4AP or TRUSS, a protein proposed to function as a scaffold protein in cell signalling processes and as a cell cycle regulator. It is conceivable that NR3 does not function as a transcription factor in contrast to bona fide NRs and that the putative LBD may function as an allosteric switch to control functional activity. To investigate the idea that NR3 may possess a fold similar to the LBD of NRs preliminary structural work has been undertaken, which has suggested the putative LBD folds into an autonomous domain as it is region resistant to proteolysis. In addition, the potential role of the putative LBD fold as a molecular switch was examined by using constitutively active fusion proteins in reporter gene assays. It was determined that the putative NR3 LBD acts in a repressive manner, potentially due to the alteration in subcellular localisation exerted by the putative NR3 LBD on the fusion protein. To further assess the role of the putative LBD a ligand screen was undertaken to identify compounds that may reduce its repressive activity, however no ligand was identified and it is conceivable NR3 may act in a ligand independent manner similar to some orphan receptors. Initial analysis of NR3 function indicates that its expression may have a positive effect on cell proliferation. To further assess the role of NR3 protein interaction assays were established to screen for binding partners. This identified the E3 ubiquitin ligase component DNA damage-binding protein 1 (DDB1) as an interacting protein involved in the regulation of cell cycle progression and DNA repair. Mapping studies suggest NR3 binds to the substrate docking site of DDB1 and further analysis showed NR3 to be ubiquitinated, affecting the stability of the protein. It is reported that the arylhydrocarbon receptor binds to a DDB1 complex, which then acts as a ligand regulated E3 ubiquitin ligase complex (Ohtake et al, 2007). This raises the possibility that NR3 may act in functionally analogous manner. To address NR3 function within the whole organism a targeting vector designed to inactivate the NR3 gene has been generated and currently a conditional knockout mouse line are being bred.
Supervisor: Parker, Malcolm Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.506959  DOI: Not available
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