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Surprising Features of Nuclear Receptor Interaction Networks Revealed by Live Cell Single Molecule Imaging
Type 2 Nuclear Receptors (T2NRs) require heterodimerization with a common partner, the Retinoid X Receptor (RXR), to bind cognate DNA recognition sites in chromatin. Based on previous biochemical and over-expression studies, binding of T2NRs to chromatin is proposed to be regulated by competition fo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516011/ https://www.ncbi.nlm.nih.gov/pubmed/37745337 http://dx.doi.org/10.1101/2023.09.16.558083 |
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author | Dahal, Liza Graham, Thomas GW Dailey, Gina M Heckert, Alec Tjian, Robert Darzacq, Xavier |
author_facet | Dahal, Liza Graham, Thomas GW Dailey, Gina M Heckert, Alec Tjian, Robert Darzacq, Xavier |
author_sort | Dahal, Liza |
collection | PubMed |
description | Type 2 Nuclear Receptors (T2NRs) require heterodimerization with a common partner, the Retinoid X Receptor (RXR), to bind cognate DNA recognition sites in chromatin. Based on previous biochemical and over-expression studies, binding of T2NRs to chromatin is proposed to be regulated by competition for a limiting pool of the core RXR subunit. However, this mechanism has not yet been tested for endogenous proteins in live cells. Using single molecule tracking (SMT) and proximity-assisted photoactivation (PAPA), we monitored interactions between endogenously tagged retinoid X receptor (RXR) and retinoic acid receptor (RAR) in live cells. Unexpectedly, we find that higher expression of RAR, but not RXR increases heterodimerization and chromatin binding in U2OS cells. This surprising finding indicates the limiting factor is not RXR but likely its cadre of obligate dimer binding partners. SMT and PAPA thus provide a direct way to probe which components are functionally limiting within a complex TF interaction network providing new insights into mechanisms of gene regulation in vivo with implications for drug development targeting nuclear receptors. |
format | Online Article Text |
id | pubmed-10516011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105160112023-09-23 Surprising Features of Nuclear Receptor Interaction Networks Revealed by Live Cell Single Molecule Imaging Dahal, Liza Graham, Thomas GW Dailey, Gina M Heckert, Alec Tjian, Robert Darzacq, Xavier bioRxiv Article Type 2 Nuclear Receptors (T2NRs) require heterodimerization with a common partner, the Retinoid X Receptor (RXR), to bind cognate DNA recognition sites in chromatin. Based on previous biochemical and over-expression studies, binding of T2NRs to chromatin is proposed to be regulated by competition for a limiting pool of the core RXR subunit. However, this mechanism has not yet been tested for endogenous proteins in live cells. Using single molecule tracking (SMT) and proximity-assisted photoactivation (PAPA), we monitored interactions between endogenously tagged retinoid X receptor (RXR) and retinoic acid receptor (RAR) in live cells. Unexpectedly, we find that higher expression of RAR, but not RXR increases heterodimerization and chromatin binding in U2OS cells. This surprising finding indicates the limiting factor is not RXR but likely its cadre of obligate dimer binding partners. SMT and PAPA thus provide a direct way to probe which components are functionally limiting within a complex TF interaction network providing new insights into mechanisms of gene regulation in vivo with implications for drug development targeting nuclear receptors. Cold Spring Harbor Laboratory 2023-10-02 /pmc/articles/PMC10516011/ /pubmed/37745337 http://dx.doi.org/10.1101/2023.09.16.558083 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Dahal, Liza Graham, Thomas GW Dailey, Gina M Heckert, Alec Tjian, Robert Darzacq, Xavier Surprising Features of Nuclear Receptor Interaction Networks Revealed by Live Cell Single Molecule Imaging |
title | Surprising Features of Nuclear Receptor Interaction Networks Revealed by Live Cell Single Molecule Imaging |
title_full | Surprising Features of Nuclear Receptor Interaction Networks Revealed by Live Cell Single Molecule Imaging |
title_fullStr | Surprising Features of Nuclear Receptor Interaction Networks Revealed by Live Cell Single Molecule Imaging |
title_full_unstemmed | Surprising Features of Nuclear Receptor Interaction Networks Revealed by Live Cell Single Molecule Imaging |
title_short | Surprising Features of Nuclear Receptor Interaction Networks Revealed by Live Cell Single Molecule Imaging |
title_sort | surprising features of nuclear receptor interaction networks revealed by live cell single molecule imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516011/ https://www.ncbi.nlm.nih.gov/pubmed/37745337 http://dx.doi.org/10.1101/2023.09.16.558083 |
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