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Construction of reporter gene assays using CWP and PDR mutant yeasts for enhanced detection of various sex steroids
BACKGROUND: Sex steroid hormone receptors are classified into three classes of receptors: estrogen receptors (ER) α and β, androgen receptor (AR), and progesterone receptor (PR). They belong to the nuclear receptor superfamily and activate their downstream genes in a ligand-dependent manner. Since s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251871/ https://www.ncbi.nlm.nih.gov/pubmed/32514322 http://dx.doi.org/10.1186/s41021-020-00159-x |
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author | Ito-Harashima, Sayoko Matano, Mami Onishi, Kana Nomura, Tomofumi Nakajima, Saki Ebata, Shingo Shiizaki, Kazuhiro Kawanishi, Masanobu Yagi, Takashi |
author_facet | Ito-Harashima, Sayoko Matano, Mami Onishi, Kana Nomura, Tomofumi Nakajima, Saki Ebata, Shingo Shiizaki, Kazuhiro Kawanishi, Masanobu Yagi, Takashi |
author_sort | Ito-Harashima, Sayoko |
collection | PubMed |
description | BACKGROUND: Sex steroid hormone receptors are classified into three classes of receptors: estrogen receptors (ER) α and β, androgen receptor (AR), and progesterone receptor (PR). They belong to the nuclear receptor superfamily and activate their downstream genes in a ligand-dependent manner. Since sex steroid hormones are involved in a wide variety of physiological processes and cancer development, synthetic chemical substances that exhibit sex steroid hormone activities have been applied as pharmaceuticals and consumed in large amounts worldwide. They are potentially hazardous contaminants as endocrine disruptors in the environment because they may induce inappropriate gene expression mediated by sex steroid hormone receptors in vivo. RESULTS: To develop simple reporter gene assays with enhanced sensitivity for the detection of sex steroid hormones, we newly established mutant yeast strains lacking the CWP and PDR genes encoding cell wall mannoproteins and plasma membrane drug efflux pumps, respectively, and expressing human ERα, ERβ, AR, and PR. Reporter gene assays with mutant yeast strains responded to endogenous and synthetic ligands more strongly than those with wild-type strains. Sex steroid hormone activities in some pharmaceutical oral tablets and human urine were also detectable in these yeast assays. CONCLUSIONS: Yeast reporter gene assay systems for all six steroid hormone receptors, including previously established glucocorticoid receptor (GR) and mineralocorticoid receptor (MR) assay yeasts, are now available. Environmental endocrine disrupters with steroid hormone activity will be qualitatively detectable by simple and easy procedures. The yeast-based reporter gene assay will be valuable as a primary screening tool to detect and evaluate steroid hormone activities in various test samples. Our assay system will strongly support the detection of agonists, antagonists, and inverse agonists of steroid hormone receptors in the field of novel drug discovery and assessments of environmental pollutants. |
format | Online Article Text |
id | pubmed-7251871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72518712020-06-07 Construction of reporter gene assays using CWP and PDR mutant yeasts for enhanced detection of various sex steroids Ito-Harashima, Sayoko Matano, Mami Onishi, Kana Nomura, Tomofumi Nakajima, Saki Ebata, Shingo Shiizaki, Kazuhiro Kawanishi, Masanobu Yagi, Takashi Genes Environ Research BACKGROUND: Sex steroid hormone receptors are classified into three classes of receptors: estrogen receptors (ER) α and β, androgen receptor (AR), and progesterone receptor (PR). They belong to the nuclear receptor superfamily and activate their downstream genes in a ligand-dependent manner. Since sex steroid hormones are involved in a wide variety of physiological processes and cancer development, synthetic chemical substances that exhibit sex steroid hormone activities have been applied as pharmaceuticals and consumed in large amounts worldwide. They are potentially hazardous contaminants as endocrine disruptors in the environment because they may induce inappropriate gene expression mediated by sex steroid hormone receptors in vivo. RESULTS: To develop simple reporter gene assays with enhanced sensitivity for the detection of sex steroid hormones, we newly established mutant yeast strains lacking the CWP and PDR genes encoding cell wall mannoproteins and plasma membrane drug efflux pumps, respectively, and expressing human ERα, ERβ, AR, and PR. Reporter gene assays with mutant yeast strains responded to endogenous and synthetic ligands more strongly than those with wild-type strains. Sex steroid hormone activities in some pharmaceutical oral tablets and human urine were also detectable in these yeast assays. CONCLUSIONS: Yeast reporter gene assay systems for all six steroid hormone receptors, including previously established glucocorticoid receptor (GR) and mineralocorticoid receptor (MR) assay yeasts, are now available. Environmental endocrine disrupters with steroid hormone activity will be qualitatively detectable by simple and easy procedures. The yeast-based reporter gene assay will be valuable as a primary screening tool to detect and evaluate steroid hormone activities in various test samples. Our assay system will strongly support the detection of agonists, antagonists, and inverse agonists of steroid hormone receptors in the field of novel drug discovery and assessments of environmental pollutants. BioMed Central 2020-05-27 /pmc/articles/PMC7251871/ /pubmed/32514322 http://dx.doi.org/10.1186/s41021-020-00159-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ito-Harashima, Sayoko Matano, Mami Onishi, Kana Nomura, Tomofumi Nakajima, Saki Ebata, Shingo Shiizaki, Kazuhiro Kawanishi, Masanobu Yagi, Takashi Construction of reporter gene assays using CWP and PDR mutant yeasts for enhanced detection of various sex steroids |
title | Construction of reporter gene assays using CWP and PDR mutant yeasts for enhanced detection of various sex steroids |
title_full | Construction of reporter gene assays using CWP and PDR mutant yeasts for enhanced detection of various sex steroids |
title_fullStr | Construction of reporter gene assays using CWP and PDR mutant yeasts for enhanced detection of various sex steroids |
title_full_unstemmed | Construction of reporter gene assays using CWP and PDR mutant yeasts for enhanced detection of various sex steroids |
title_short | Construction of reporter gene assays using CWP and PDR mutant yeasts for enhanced detection of various sex steroids |
title_sort | construction of reporter gene assays using cwp and pdr mutant yeasts for enhanced detection of various sex steroids |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251871/ https://www.ncbi.nlm.nih.gov/pubmed/32514322 http://dx.doi.org/10.1186/s41021-020-00159-x |
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