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Androgen response element of the glycine N-methyltransferase gene is located in the coding region of its first exon

Androgen plays an important role in the pathogenesis of PCa (prostate cancer). Previously, we identified GNMT (glycine N-methyltransferase) as a tumour susceptibility gene and characterized its promoter region. Besides, its enzymatic product-sarcosine has been recognized as a marker for prognosis of...

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Autores principales: Lee, Cheng-Ming, Yen, Chia-Hung, Tzeng, Tsai-Yu, Huang, Yu-Zen, Chou, Kuan-Hsien, Chang, Tai-Jay, Arthur Chen, Yi-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775523/
https://www.ncbi.nlm.nih.gov/pubmed/23883094
http://dx.doi.org/10.1042/BSR20130030
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author Lee, Cheng-Ming
Yen, Chia-Hung
Tzeng, Tsai-Yu
Huang, Yu-Zen
Chou, Kuan-Hsien
Chang, Tai-Jay
Arthur Chen, Yi-Ming
author_facet Lee, Cheng-Ming
Yen, Chia-Hung
Tzeng, Tsai-Yu
Huang, Yu-Zen
Chou, Kuan-Hsien
Chang, Tai-Jay
Arthur Chen, Yi-Ming
author_sort Lee, Cheng-Ming
collection PubMed
description Androgen plays an important role in the pathogenesis of PCa (prostate cancer). Previously, we identified GNMT (glycine N-methyltransferase) as a tumour susceptibility gene and characterized its promoter region. Besides, its enzymatic product-sarcosine has been recognized as a marker for prognosis of PCa. The goals of this study were to determine whether GNMT is regulated by androgen and to map its AREs (androgen response elements). Real-time PCR analyses showed that R1881, a synthetic AR (androgen receptor) agonist induced GNMT expression in AR-positive LNCaP cells, but not in AR-negative DU145 cells. In silico prediction showed that there are four putative AREs in GNMT-ARE1, ARE2 and ARE3 are located in the intron 1 and ARE4 is in the intron 2. Consensus ARE motif deduced from published AREs was used to identify the fifth ARE-ARE5 in the coding region of exon 1. Luciferase reporter assay found that only ARE5 mediated the transcriptional activation of R1881. ARE3 overlaps with a YY1 [Yin and Yang 1 (motif (CaCCATGTT, +1118/+1126)] that was further confirmed by antibody supershift and ChIP (chromatin immunoprecipitation) assays. EMSA (electrophoretic mobility shift assay) and ChIP assay confirmed that AR interacts with ARE5 in vitro and in vivo. In summary, GNMT is an AR-targeted gene with its functional ARE located at +19/+33 of the first exon. These results are valuable for the study of the influence of androgen on the gene expression of GNMT especially in the pathogenesis of cancer.
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spelling pubmed-37755232013-09-17 Androgen response element of the glycine N-methyltransferase gene is located in the coding region of its first exon Lee, Cheng-Ming Yen, Chia-Hung Tzeng, Tsai-Yu Huang, Yu-Zen Chou, Kuan-Hsien Chang, Tai-Jay Arthur Chen, Yi-Ming Biosci Rep Original Paper Androgen plays an important role in the pathogenesis of PCa (prostate cancer). Previously, we identified GNMT (glycine N-methyltransferase) as a tumour susceptibility gene and characterized its promoter region. Besides, its enzymatic product-sarcosine has been recognized as a marker for prognosis of PCa. The goals of this study were to determine whether GNMT is regulated by androgen and to map its AREs (androgen response elements). Real-time PCR analyses showed that R1881, a synthetic AR (androgen receptor) agonist induced GNMT expression in AR-positive LNCaP cells, but not in AR-negative DU145 cells. In silico prediction showed that there are four putative AREs in GNMT-ARE1, ARE2 and ARE3 are located in the intron 1 and ARE4 is in the intron 2. Consensus ARE motif deduced from published AREs was used to identify the fifth ARE-ARE5 in the coding region of exon 1. Luciferase reporter assay found that only ARE5 mediated the transcriptional activation of R1881. ARE3 overlaps with a YY1 [Yin and Yang 1 (motif (CaCCATGTT, +1118/+1126)] that was further confirmed by antibody supershift and ChIP (chromatin immunoprecipitation) assays. EMSA (electrophoretic mobility shift assay) and ChIP assay confirmed that AR interacts with ARE5 in vitro and in vivo. In summary, GNMT is an AR-targeted gene with its functional ARE located at +19/+33 of the first exon. These results are valuable for the study of the influence of androgen on the gene expression of GNMT especially in the pathogenesis of cancer. Portland Press Ltd. 2013-09-17 /pmc/articles/PMC3775523/ /pubmed/23883094 http://dx.doi.org/10.1042/BSR20130030 Text en © 2013 The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Licence (CC-BY)(http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Lee, Cheng-Ming
Yen, Chia-Hung
Tzeng, Tsai-Yu
Huang, Yu-Zen
Chou, Kuan-Hsien
Chang, Tai-Jay
Arthur Chen, Yi-Ming
Androgen response element of the glycine N-methyltransferase gene is located in the coding region of its first exon
title Androgen response element of the glycine N-methyltransferase gene is located in the coding region of its first exon
title_full Androgen response element of the glycine N-methyltransferase gene is located in the coding region of its first exon
title_fullStr Androgen response element of the glycine N-methyltransferase gene is located in the coding region of its first exon
title_full_unstemmed Androgen response element of the glycine N-methyltransferase gene is located in the coding region of its first exon
title_short Androgen response element of the glycine N-methyltransferase gene is located in the coding region of its first exon
title_sort androgen response element of the glycine n-methyltransferase gene is located in the coding region of its first exon
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775523/
https://www.ncbi.nlm.nih.gov/pubmed/23883094
http://dx.doi.org/10.1042/BSR20130030
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