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Identification of G-quadruplex structures that possess transcriptional regulating functions in the Dele and Cdc6 CpG islands
BACKGROUND: G-quadruplex is a DNA secondary structure that has been shown to play an important role in biological systems. In a previous study, we identified 1998 G-quadruplex-forming sequences using a mouse CpG islands DNA microarray with a fluorescent-labeled G-quadruplex ligand. Among these putat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488298/ https://www.ncbi.nlm.nih.gov/pubmed/28655335 http://dx.doi.org/10.1186/s12867-017-0094-z |
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author | Bay, Daniyah H. Busch, Annika Lisdat, Fred Iida, Keisuke Ikebukuro, Kazunori Nagasawa, Kazuo Karube, Isao Yoshida, Wataru |
author_facet | Bay, Daniyah H. Busch, Annika Lisdat, Fred Iida, Keisuke Ikebukuro, Kazunori Nagasawa, Kazuo Karube, Isao Yoshida, Wataru |
author_sort | Bay, Daniyah H. |
collection | PubMed |
description | BACKGROUND: G-quadruplex is a DNA secondary structure that has been shown to play an important role in biological systems. In a previous study, we identified 1998 G-quadruplex-forming sequences using a mouse CpG islands DNA microarray with a fluorescent-labeled G-quadruplex ligand. Among these putative G-quadruplex-forming sequences, G-quadruplex formation was verified for 10 randomly selected sequences by CD spectroscopy and DMS footprinting analysis. In this study, the biological function of the 10 G-quadruplex-forming sequences in the transcriptional regulation has been analyzed using a reporter assay. RESULTS: When G-quadruplex-forming sequences from the Dele and Cdc6 genes have been cloned in reporter vectors carrying a minimal promoter and the luciferase gene, luciferase expression is activated. This has also been detected in experiments applying a promoterless reporter vector. Mutational analysis reveals that guanine bases, which form the G-tetrads, are important in the activation. In addition, the activation has been found to decrease by the telomestatin derivative L1H1-7OTD which can bind to the G-quadruplex DNA. When Dele and Cdc6 CpG islands, containing the G-quadruplex-forming sequence, have been cloned in the promoterless reporter vector, the luciferase expression is activated. Mutational analysis reveals that the expression level is decreased by mutation on Dele G-quadruplex; however, increased by mutation on Cdc6 G-quadruplex. CONCLUSION: Dele and Cdc6 G-quadruplex formation is significant in the transcriptional regulation. Dele and Cdc6 G-quadruplex DNA alone possess enhancer and promotor function. When studied in more complex CpG islands Dele G-quadruplex also demonstrates promotor activity, whereas Cdc6 G-quadruplex may possess a dual function of transcriptional regulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12867-017-0094-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5488298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54882982017-07-03 Identification of G-quadruplex structures that possess transcriptional regulating functions in the Dele and Cdc6 CpG islands Bay, Daniyah H. Busch, Annika Lisdat, Fred Iida, Keisuke Ikebukuro, Kazunori Nagasawa, Kazuo Karube, Isao Yoshida, Wataru BMC Mol Biol Research Article BACKGROUND: G-quadruplex is a DNA secondary structure that has been shown to play an important role in biological systems. In a previous study, we identified 1998 G-quadruplex-forming sequences using a mouse CpG islands DNA microarray with a fluorescent-labeled G-quadruplex ligand. Among these putative G-quadruplex-forming sequences, G-quadruplex formation was verified for 10 randomly selected sequences by CD spectroscopy and DMS footprinting analysis. In this study, the biological function of the 10 G-quadruplex-forming sequences in the transcriptional regulation has been analyzed using a reporter assay. RESULTS: When G-quadruplex-forming sequences from the Dele and Cdc6 genes have been cloned in reporter vectors carrying a minimal promoter and the luciferase gene, luciferase expression is activated. This has also been detected in experiments applying a promoterless reporter vector. Mutational analysis reveals that guanine bases, which form the G-tetrads, are important in the activation. In addition, the activation has been found to decrease by the telomestatin derivative L1H1-7OTD which can bind to the G-quadruplex DNA. When Dele and Cdc6 CpG islands, containing the G-quadruplex-forming sequence, have been cloned in the promoterless reporter vector, the luciferase expression is activated. Mutational analysis reveals that the expression level is decreased by mutation on Dele G-quadruplex; however, increased by mutation on Cdc6 G-quadruplex. CONCLUSION: Dele and Cdc6 G-quadruplex formation is significant in the transcriptional regulation. Dele and Cdc6 G-quadruplex DNA alone possess enhancer and promotor function. When studied in more complex CpG islands Dele G-quadruplex also demonstrates promotor activity, whereas Cdc6 G-quadruplex may possess a dual function of transcriptional regulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12867-017-0094-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-27 /pmc/articles/PMC5488298/ /pubmed/28655335 http://dx.doi.org/10.1186/s12867-017-0094-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Article Bay, Daniyah H. Busch, Annika Lisdat, Fred Iida, Keisuke Ikebukuro, Kazunori Nagasawa, Kazuo Karube, Isao Yoshida, Wataru Identification of G-quadruplex structures that possess transcriptional regulating functions in the Dele and Cdc6 CpG islands |
title | Identification of G-quadruplex structures that possess transcriptional regulating functions in the Dele and Cdc6 CpG islands |
title_full | Identification of G-quadruplex structures that possess transcriptional regulating functions in the Dele and Cdc6 CpG islands |
title_fullStr | Identification of G-quadruplex structures that possess transcriptional regulating functions in the Dele and Cdc6 CpG islands |
title_full_unstemmed | Identification of G-quadruplex structures that possess transcriptional regulating functions in the Dele and Cdc6 CpG islands |
title_short | Identification of G-quadruplex structures that possess transcriptional regulating functions in the Dele and Cdc6 CpG islands |
title_sort | identification of g-quadruplex structures that possess transcriptional regulating functions in the dele and cdc6 cpg islands |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488298/ https://www.ncbi.nlm.nih.gov/pubmed/28655335 http://dx.doi.org/10.1186/s12867-017-0094-z |
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