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Identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of HepG2 cells

All-trans retinoic acid (ATRA) is a potent inducer of cell differentiation and growth arrest. Here, we investigated ATRA-induced regulatory cascades associated with growth arrest of the human hepatoma cell line HepG2. ATRA induced >2-fold changes in the expression of 402 genes including 55 linked...

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Autores principales: Nakanishi, Misato, Tomaru, Yasuhiro, Miura, Hisashi, Hayashizaki, Yoshihide, Suzuki, Masanori
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2425469/
https://www.ncbi.nlm.nih.gov/pubmed/18445634
http://dx.doi.org/10.1093/nar/gkn066
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author Nakanishi, Misato
Tomaru, Yasuhiro
Miura, Hisashi
Hayashizaki, Yoshihide
Suzuki, Masanori
author_facet Nakanishi, Misato
Tomaru, Yasuhiro
Miura, Hisashi
Hayashizaki, Yoshihide
Suzuki, Masanori
author_sort Nakanishi, Misato
collection PubMed
description All-trans retinoic acid (ATRA) is a potent inducer of cell differentiation and growth arrest. Here, we investigated ATRA-induced regulatory cascades associated with growth arrest of the human hepatoma cell line HepG2. ATRA induced >2-fold changes in the expression of 402 genes including 55 linked to cell-cycle regulation, cell growth or apoptosis during 48 h treatment. Computational search predicted that 250 transcriptional regulatory factors (TRFs) could recognize the proximal upstream regions of any of the 55 genes. Expression of 61 TRF genes was significantly changed during ATRA incubation, providing many potential regulatory edges. We focused on six TRFs that could regulate many of the 55 genes and found a total of 160 potential edges in which the expression of each of the genes was changed later than the expression change of the corresponding regulator. RNAi knockdown of the selected TRFs caused perturbation of the respective potential targets. The genes showed an opposite regulation pattern by ATRA and specific siRNA treatments were selected as strong candidates for direct TRF targets. Finally, 36 transcriptional regulatory edges were validated by chromatin immunoprecipitation. These analyses enabled us to depict a part of the transcriptional regulatory cascades closely linked to ATRA-induced cell growth arrest.
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spelling pubmed-24254692008-06-12 Identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of HepG2 cells Nakanishi, Misato Tomaru, Yasuhiro Miura, Hisashi Hayashizaki, Yoshihide Suzuki, Masanori Nucleic Acids Res Molecular Biology All-trans retinoic acid (ATRA) is a potent inducer of cell differentiation and growth arrest. Here, we investigated ATRA-induced regulatory cascades associated with growth arrest of the human hepatoma cell line HepG2. ATRA induced >2-fold changes in the expression of 402 genes including 55 linked to cell-cycle regulation, cell growth or apoptosis during 48 h treatment. Computational search predicted that 250 transcriptional regulatory factors (TRFs) could recognize the proximal upstream regions of any of the 55 genes. Expression of 61 TRF genes was significantly changed during ATRA incubation, providing many potential regulatory edges. We focused on six TRFs that could regulate many of the 55 genes and found a total of 160 potential edges in which the expression of each of the genes was changed later than the expression change of the corresponding regulator. RNAi knockdown of the selected TRFs caused perturbation of the respective potential targets. The genes showed an opposite regulation pattern by ATRA and specific siRNA treatments were selected as strong candidates for direct TRF targets. Finally, 36 transcriptional regulatory edges were validated by chromatin immunoprecipitation. These analyses enabled us to depict a part of the transcriptional regulatory cascades closely linked to ATRA-induced cell growth arrest. Oxford University Press 2008-06 2008-04-29 /pmc/articles/PMC2425469/ /pubmed/18445634 http://dx.doi.org/10.1093/nar/gkn066 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Nakanishi, Misato
Tomaru, Yasuhiro
Miura, Hisashi
Hayashizaki, Yoshihide
Suzuki, Masanori
Identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of HepG2 cells
title Identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of HepG2 cells
title_full Identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of HepG2 cells
title_fullStr Identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of HepG2 cells
title_full_unstemmed Identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of HepG2 cells
title_short Identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of HepG2 cells
title_sort identification of transcriptional regulatory cascades in retinoic acid-induced growth arrest of hepg2 cells
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2425469/
https://www.ncbi.nlm.nih.gov/pubmed/18445634
http://dx.doi.org/10.1093/nar/gkn066
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