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Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1

Yin Yang 1 (YY1) is a multifunctional protein with regulatory potential in tumorigenesis. Ample studies demonstrated the activities of YY1 in regulating gene expression and mediating differential protein modifications. However, the mechanisms underlying YY1 gene expression are relatively understudie...

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Autores principales: Huang, Weiwei, Smaldino, Philip J., Zhang, Qiang, Miller, Lance D., Cao, Paul, Stadelman, Kristin, Wan, Meimei, Giri, Banabihari, Lei, Ming, Nagamine, Yoshikuni, Vaughn, James P., Akman, Steven A., Sui, Guangchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3273823/
https://www.ncbi.nlm.nih.gov/pubmed/21993297
http://dx.doi.org/10.1093/nar/gkr849
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author Huang, Weiwei
Smaldino, Philip J.
Zhang, Qiang
Miller, Lance D.
Cao, Paul
Stadelman, Kristin
Wan, Meimei
Giri, Banabihari
Lei, Ming
Nagamine, Yoshikuni
Vaughn, James P.
Akman, Steven A.
Sui, Guangchao
author_facet Huang, Weiwei
Smaldino, Philip J.
Zhang, Qiang
Miller, Lance D.
Cao, Paul
Stadelman, Kristin
Wan, Meimei
Giri, Banabihari
Lei, Ming
Nagamine, Yoshikuni
Vaughn, James P.
Akman, Steven A.
Sui, Guangchao
author_sort Huang, Weiwei
collection PubMed
description Yin Yang 1 (YY1) is a multifunctional protein with regulatory potential in tumorigenesis. Ample studies demonstrated the activities of YY1 in regulating gene expression and mediating differential protein modifications. However, the mechanisms underlying YY1 gene expression are relatively understudied. G-quadruplexes (G4s) are four-stranded structures or motifs formed by guanine-rich DNA or RNA domains. The presence of G4 structures in a gene promoter or the 5′-UTR of its mRNA can markedly affect its expression. In this report, we provide strong evidence showing the presence of G4 structures in the promoter and the 5′-UTR of YY1. In reporter assays, mutations in these G4 structure forming sequences increased the expression of Gaussia luciferase (Gluc) downstream of either YY1 promoter or 5′-UTR. We also discovered that G4 Resolvase 1 (G4R1) enhanced the Gluc expression mediated by the YY1 promoter, but not the YY1 5′-UTR. Consistently, G4R1 binds the G4 motif of the YY1 promoter in vitro and ectopically expressed G4R1 increased endogenous YY1 levels. In addition, the analysis of a gene array data consisting of the breast cancer samples of 258 patients also indicates a significant, positive correlation between G4R1 and YY1 expression.
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spelling pubmed-32738232012-02-07 Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1 Huang, Weiwei Smaldino, Philip J. Zhang, Qiang Miller, Lance D. Cao, Paul Stadelman, Kristin Wan, Meimei Giri, Banabihari Lei, Ming Nagamine, Yoshikuni Vaughn, James P. Akman, Steven A. Sui, Guangchao Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Yin Yang 1 (YY1) is a multifunctional protein with regulatory potential in tumorigenesis. Ample studies demonstrated the activities of YY1 in regulating gene expression and mediating differential protein modifications. However, the mechanisms underlying YY1 gene expression are relatively understudied. G-quadruplexes (G4s) are four-stranded structures or motifs formed by guanine-rich DNA or RNA domains. The presence of G4 structures in a gene promoter or the 5′-UTR of its mRNA can markedly affect its expression. In this report, we provide strong evidence showing the presence of G4 structures in the promoter and the 5′-UTR of YY1. In reporter assays, mutations in these G4 structure forming sequences increased the expression of Gaussia luciferase (Gluc) downstream of either YY1 promoter or 5′-UTR. We also discovered that G4 Resolvase 1 (G4R1) enhanced the Gluc expression mediated by the YY1 promoter, but not the YY1 5′-UTR. Consistently, G4R1 binds the G4 motif of the YY1 promoter in vitro and ectopically expressed G4R1 increased endogenous YY1 levels. In addition, the analysis of a gene array data consisting of the breast cancer samples of 258 patients also indicates a significant, positive correlation between G4R1 and YY1 expression. Oxford University Press 2012-02 2011-10-12 /pmc/articles/PMC3273823/ /pubmed/21993297 http://dx.doi.org/10.1093/nar/gkr849 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene Regulation, Chromatin and Epigenetics
Huang, Weiwei
Smaldino, Philip J.
Zhang, Qiang
Miller, Lance D.
Cao, Paul
Stadelman, Kristin
Wan, Meimei
Giri, Banabihari
Lei, Ming
Nagamine, Yoshikuni
Vaughn, James P.
Akman, Steven A.
Sui, Guangchao
Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1
title Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1
title_full Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1
title_fullStr Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1
title_full_unstemmed Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1
title_short Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1
title_sort yin yang 1 contains g-quadruplex structures in its promoter and 5′-utr and its expression is modulated by g4 resolvase 1
topic Gene Regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3273823/
https://www.ncbi.nlm.nih.gov/pubmed/21993297
http://dx.doi.org/10.1093/nar/gkr849
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