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Global mapping of ZBTB7A transcription factor binding sites in HepG2 cells

ZBTB7A is a known proto-oncogene that is implicated in carcinogenesis and cell differentiation and development. Fully understanding the function of ZBTB7A in cellular processes could provide useful strategies for cancer treatment and development-associated disease therapy. Here, global mapping of ZB...

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Detalles Bibliográficos
Autores principales: Zu, Xuyu, Yu, Lingling, Sun, Yiming, Tian, Jing, Liu, Feng, Sun, Qinsheng, He, Shengnan, Sun, Guang, Luo, Weishi, Jiang, Yuyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SP Versita 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275666/
https://www.ncbi.nlm.nih.gov/pubmed/20336405
http://dx.doi.org/10.2478/s11658-010-0003-7
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author Zu, Xuyu
Yu, Lingling
Sun, Yiming
Tian, Jing
Liu, Feng
Sun, Qinsheng
He, Shengnan
Sun, Guang
Luo, Weishi
Jiang, Yuyang
author_facet Zu, Xuyu
Yu, Lingling
Sun, Yiming
Tian, Jing
Liu, Feng
Sun, Qinsheng
He, Shengnan
Sun, Guang
Luo, Weishi
Jiang, Yuyang
author_sort Zu, Xuyu
collection PubMed
description ZBTB7A is a known proto-oncogene that is implicated in carcinogenesis and cell differentiation and development. Fully understanding the function of ZBTB7A in cellular processes could provide useful strategies for cancer treatment and development-associated disease therapy. Here, global mapping of ZBTB7A transcription factor binding sites was developed by utilizing microarray technology in HepG2 cells. The data obtained from the microarrays was further validated via chromatin immunoprecipitation-PCR (ChIP-PCR) and real time-PCR, and it was revealed that ZBTB7A may be one of the regulators of neural development. ZBTB7A target signal pathways were identified in signal pathway and GO (Gene Ontology) analyses. This is the first report on the global mapping of ZBTB7A downstream direct targets, and these findings will be useful in understanding the roles of ZBTB7A in cellular processes.
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spelling pubmed-62756662018-12-10 Global mapping of ZBTB7A transcription factor binding sites in HepG2 cells Zu, Xuyu Yu, Lingling Sun, Yiming Tian, Jing Liu, Feng Sun, Qinsheng He, Shengnan Sun, Guang Luo, Weishi Jiang, Yuyang Cell Mol Biol Lett Research Article ZBTB7A is a known proto-oncogene that is implicated in carcinogenesis and cell differentiation and development. Fully understanding the function of ZBTB7A in cellular processes could provide useful strategies for cancer treatment and development-associated disease therapy. Here, global mapping of ZBTB7A transcription factor binding sites was developed by utilizing microarray technology in HepG2 cells. The data obtained from the microarrays was further validated via chromatin immunoprecipitation-PCR (ChIP-PCR) and real time-PCR, and it was revealed that ZBTB7A may be one of the regulators of neural development. ZBTB7A target signal pathways were identified in signal pathway and GO (Gene Ontology) analyses. This is the first report on the global mapping of ZBTB7A downstream direct targets, and these findings will be useful in understanding the roles of ZBTB7A in cellular processes. SP Versita 2010-03-19 /pmc/articles/PMC6275666/ /pubmed/20336405 http://dx.doi.org/10.2478/s11658-010-0003-7 Text en © © Versita Warsaw and Springer-Verlag Wien 2010
spellingShingle Research Article
Zu, Xuyu
Yu, Lingling
Sun, Yiming
Tian, Jing
Liu, Feng
Sun, Qinsheng
He, Shengnan
Sun, Guang
Luo, Weishi
Jiang, Yuyang
Global mapping of ZBTB7A transcription factor binding sites in HepG2 cells
title Global mapping of ZBTB7A transcription factor binding sites in HepG2 cells
title_full Global mapping of ZBTB7A transcription factor binding sites in HepG2 cells
title_fullStr Global mapping of ZBTB7A transcription factor binding sites in HepG2 cells
title_full_unstemmed Global mapping of ZBTB7A transcription factor binding sites in HepG2 cells
title_short Global mapping of ZBTB7A transcription factor binding sites in HepG2 cells
title_sort global mapping of zbtb7a transcription factor binding sites in hepg2 cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275666/
https://www.ncbi.nlm.nih.gov/pubmed/20336405
http://dx.doi.org/10.2478/s11658-010-0003-7
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