Joel Fulton
Heterodimers of photoreceptor-specific nuclear receptor (PNR/NR2E3) and peroxisome proliferator-activated receptor (PPAR?) are disrupted by retinal disease-associated mutations
Fulton, Joel; Mazumder, Bismoy; Whitchurch, Jonathan; Monteiro, Cintia J.; Collins, Hilary M.; Chan, Chun M.; Clemente, Maria P.; Hernandez Quiles, Miguel; Stewart, Elizabeth A.; Amoaku, Winfried; Moran, Paula M.; Mongan, Nigel P.; Persson, Jenny L.; Ali, Simak; Heery, David M.
Authors
Bismoy Mazumder
Jonathan Whitchurch
Cintia J. Monteiro
HILARY COLLINS HILARY.COLLINS@NOTTINGHAM.AC.UK
Scientific Officer
Chun M. Chan
Maria P. Clemente
Miguel Hernandez Quiles
Elizabeth A. Stewart
WINFRIED AMOAKU winfried.amoaku@nottingham.ac.uk
Clinical Assoc Prof & Reader in Ophthalmology & Visual Sciences
Paula M. Moran
NIGEL MONGAN nigel.mongan@nottingham.ac.uk
Professor of Oncology
Jenny L. Persson
Simak Ali
DAVID HEERY david.heery@nottingham.ac.uk
Professor of Eucaryotic Gene Regulation
Abstract
Photoreceptor-specific nuclear receptor (PNR/NR2E3) and Tailless homolog (TLX/NR2E1) are human orthologs of the NR2E group, a subgroup of phylogenetically related members of the Nuclear Receptor (NR) superfamily of transcription factors. We assessed the ability of these NRs to form heterodimers with other members of the human NRs representing all major subgroups. The TLX ligand binding domain (LBD) did not appear to form homodimers or interact directly with any other NR tested. The PNR LBD was able to form homodimers, but also exhibited robust interactions with the LBDs of PPAR?/NR1C3 and TR?/NR1A2. The binding of PNR to PPAR? was specific for this paralog, as no interaction was observed with the LBDs of PPAR?NR1C1 or PPAR?NR1C2. In support of these findings, PPAR? and PNR were found to be co-expressed in human retinal tissue extracts and could be co-immunoprecipitated as a native complex. Selected sequence variants in the PNR LBD associated with human retinopathies, or a mutation in the dimerization region of PPAR? LBD associated with familial partial lipodystrophy type 3, were found to disrupt PNR/PPAR? complex formation. Wild type PNR, but not a PNR309G mutant, was able to repress PPAR?-mediated transcription in reporter assays. In summary our results reveal novel heterodimer interactions in the NR superfamily, suggesting previously unknown functional interactions of PNR with PPAR? and TR? that have potential importance in retinal development and disease.
Citation
Fulton, J., Mazumder, B., Whitchurch, J., Monteiro, C. J., Collins, H. M., Chan, C. M., …Heery, D. M. (2017). Heterodimers of photoreceptor-specific nuclear receptor (PNR/NR2E3) and peroxisome proliferator-activated receptor (PPARγ) are disrupted by retinal disease-associated mutations. Cell Death and Disease, 8, Article e2677. https://doi.org/10.1038/cddis.2017.98
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 23, 2017 |
Publication Date | Mar 16, 2017 |
Deposit Date | Feb 13, 2017 |
Publicly Available Date | Mar 17, 2017 |
Journal | Cell Death and Disease |
Electronic ISSN | 2041-4889 |
Publisher | Nature Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 8 |
Article Number | e2677 |
DOI | https://doi.org/10.1038/cddis.2017.98 |
Keywords | nuclear receptor, NR2E3, NR2E1, NR1C3, photoreceptor specific nuclear receptor (PNR), Tailless (TLX), peroxisome proliferator activated receptor (PPAR), dimerization, protein, protein interaction, enhanced S-cone syndrome |
Public URL | https://nottingham-repository.worktribe.com/output/851031 |
Publisher URL | http://www.nature.com/cddis/journal/v8/n3/full/cddis201798a.html |
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Copyright Statement
Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0
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