Ubiquitination of nuclear receptors
- PMID: 28473472
- DOI: 10.1042/CS20160708
Ubiquitination of nuclear receptors
Abstract
Nuclear receptors (NRs) are cellular proteins, which upon ligand activation, act to exert regulatory control over transcription and subsequent expression. Organized via systemic classification into seven subfamilies, NRs partake in modulating a vast expanse of physiological functions essential for maintenance of life. NRs display particular characteristics towards ubiquitination, the process of addition of specific ubiquitin tags at appropriate locations. Orchestrated through groups of enzymes harboring a diverse array of specialized structural components, the ubiquitination process emphatically alters the fate or downstream effects of NRs. Such influence is especially prominent in transcriptional processes such as promoter clearing for optimization and degradation pathways eliminating or recycling targeted proteins. Ultimately, the ubiquitination of NRs carries significant implications in terms of generating pathological clinical manifestations. Increasing evidence from studies involving patients and disease models suggests a role for ubiquitinated NRs in virtually every organ system. This supports the broad repertoire of roles that NRs play in the body, including modulatory conductors, facilitators, responders to external agents, and critical constituents for pharmacological or biological interventions. This review aims to cover relevant background and mechanisms of NRs and ubiquitination, with a focus towards elucidating subsequent pathophysiology and therapeutics in clinical disorders encompassing such ubiquitinated NRs.
Keywords: clinical disorders; nuclear receptors; ubiquitination.
© 2017 The Author(s). published by Portland Press Limited on behalf of the Biochemical Society.
Similar articles
-
Transcriptional control of metabolic and inflammatory pathways by nuclear receptor SUMOylation.Biochim Biophys Acta. 2011 Aug;1812(8):909-18. doi: 10.1016/j.bbadis.2010.12.008. Epub 2010 Dec 21. Biochim Biophys Acta. 2011. PMID: 21172431 Review.
-
Evolution of the repertoire of nuclear receptor binding sites in genomes.Mol Cell Endocrinol. 2011 Mar 1;334(1-2):76-82. doi: 10.1016/j.mce.2010.10.021. Epub 2010 Nov 4. Mol Cell Endocrinol. 2011. PMID: 21056084 Review.
-
Role of nuclear receptors in the modulation of insulin secretion in lipid-induced insulin resistance.Biochem Soc Trans. 2008 Oct;36(Pt 5):891-900. doi: 10.1042/BST0360891. Biochem Soc Trans. 2008. PMID: 18793157 Review.
-
Nuclear receptor repression: regulatory mechanisms and physiological implications.Prog Mol Biol Transl Sci. 2009;87:235-59. doi: 10.1016/S1877-1173(09)87007-5. Epub 2009 Oct 7. Prog Mol Biol Transl Sci. 2009. PMID: 20374706 Review.
-
Emerging roles of the ubiquitin proteasome system in nuclear hormone receptor signaling.Prog Mol Biol Transl Sci. 2009;87:117-35. doi: 10.1016/S1877-1173(09)87004-X. Epub 2009 Oct 7. Prog Mol Biol Transl Sci. 2009. PMID: 20374703 Review.
Cited by
-
c-Cbl: An Important Regulator and a Target in Angiogenesis and Tumorigenesis.Cells. 2019 May 23;8(5):498. doi: 10.3390/cells8050498. Cells. 2019. PMID: 31126146 Free PMC article. Review.
-
Stable expression of a truncated TLX variant drives differentiation of induced pluripotent stem cells into self-renewing neural stem cells for production of extracellular vesicles.Stem Cell Res Ther. 2022 Sep 2;13(1):436. doi: 10.1186/s13287-022-03131-4. Stem Cell Res Ther. 2022. PMID: 36056423 Free PMC article.
-
Chemical Screening of Nuclear Receptor Modulators.Int J Mol Sci. 2020 Jul 31;21(15):5512. doi: 10.3390/ijms21155512. Int J Mol Sci. 2020. PMID: 32752136 Free PMC article. Review.
-
UBE2G1 Is a Critical Component of Immune Response to the Infection of Pseudomonas Plecoglossicida in Large Yellow Croaker (Larimichthys crocea).Int J Mol Sci. 2022 Jul 27;23(15):8298. doi: 10.3390/ijms23158298. Int J Mol Sci. 2022. PMID: 35955424 Free PMC article.
-
Estrogen Receptor β as a Candidate Regulator of Sex Differences in the Maternal Immune Activation Model of ASD.Front Mol Neurosci. 2021 Aug 31;14:717411. doi: 10.3389/fnmol.2021.717411. eCollection 2021. Front Mol Neurosci. 2021. PMID: 34531723 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources