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Nuclear Hormone Receptors and Their Ligands: Metabolites in Control of Transcription

Nuclear hormone receptors are a family of transcription factors regulated by small molecules derived from the endogenous metabolism or diet. There are forty-eight nuclear hormone receptors in the human genome, twenty of which are still orphans. In this review, we make a brief historical journey from...

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Autores principales: Tao, Lian Jing, Seo, Dong Eun, Jackson, Benjamin, Ivanova, Natalia B., Santori, Fabio Rinaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762034/
https://www.ncbi.nlm.nih.gov/pubmed/33291787
http://dx.doi.org/10.3390/cells9122606
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author Tao, Lian Jing
Seo, Dong Eun
Jackson, Benjamin
Ivanova, Natalia B.
Santori, Fabio Rinaldo
author_facet Tao, Lian Jing
Seo, Dong Eun
Jackson, Benjamin
Ivanova, Natalia B.
Santori, Fabio Rinaldo
author_sort Tao, Lian Jing
collection PubMed
description Nuclear hormone receptors are a family of transcription factors regulated by small molecules derived from the endogenous metabolism or diet. There are forty-eight nuclear hormone receptors in the human genome, twenty of which are still orphans. In this review, we make a brief historical journey from the first observations by Berthold in 1849 to the era of orphan receptors that began with the sequencing of the Caenorhabditis elegans genome in 1998. We discuss the evolution of nuclear hormone receptors and the putative ancestral ligands as well as how the ligand universe has expanded over time. This leads us to define four classes of metabolites—fatty acids, terpenoids, porphyrins and amino acid derivatives—that generate all known ligands for nuclear hormone receptors. We conclude by discussing the ongoing efforts to identify new classes of ligands for orphan receptors.
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spelling pubmed-77620342020-12-26 Nuclear Hormone Receptors and Their Ligands: Metabolites in Control of Transcription Tao, Lian Jing Seo, Dong Eun Jackson, Benjamin Ivanova, Natalia B. Santori, Fabio Rinaldo Cells Review Nuclear hormone receptors are a family of transcription factors regulated by small molecules derived from the endogenous metabolism or diet. There are forty-eight nuclear hormone receptors in the human genome, twenty of which are still orphans. In this review, we make a brief historical journey from the first observations by Berthold in 1849 to the era of orphan receptors that began with the sequencing of the Caenorhabditis elegans genome in 1998. We discuss the evolution of nuclear hormone receptors and the putative ancestral ligands as well as how the ligand universe has expanded over time. This leads us to define four classes of metabolites—fatty acids, terpenoids, porphyrins and amino acid derivatives—that generate all known ligands for nuclear hormone receptors. We conclude by discussing the ongoing efforts to identify new classes of ligands for orphan receptors. MDPI 2020-12-04 /pmc/articles/PMC7762034/ /pubmed/33291787 http://dx.doi.org/10.3390/cells9122606 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tao, Lian Jing
Seo, Dong Eun
Jackson, Benjamin
Ivanova, Natalia B.
Santori, Fabio Rinaldo
Nuclear Hormone Receptors and Their Ligands: Metabolites in Control of Transcription
title Nuclear Hormone Receptors and Their Ligands: Metabolites in Control of Transcription
title_full Nuclear Hormone Receptors and Their Ligands: Metabolites in Control of Transcription
title_fullStr Nuclear Hormone Receptors and Their Ligands: Metabolites in Control of Transcription
title_full_unstemmed Nuclear Hormone Receptors and Their Ligands: Metabolites in Control of Transcription
title_short Nuclear Hormone Receptors and Their Ligands: Metabolites in Control of Transcription
title_sort nuclear hormone receptors and their ligands: metabolites in control of transcription
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762034/
https://www.ncbi.nlm.nih.gov/pubmed/33291787
http://dx.doi.org/10.3390/cells9122606
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