Bioinformatic Dissecting of TP53 Regulation Pathway Underlying Butyrate-induced Histone Modification in Epigenetic Regulation

Butyrate affects cell proliferation, differentiation, and motility. Butyrate inhibits histone deacetylase (HDAC) activities and induces cell-cycle arrest and apoptosis. TP53 is one of the most active upstream regulators discovered by ingenuity pathways analysis (IPA) in our RNA-sequencing data set....

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Main Authors: Cong-Jun Li, Robert W. Li
Format: Article
Language:English
Published: SAGE Publishing 2014-01-01
Series:Genetics and Epigenetics
Online Access:https://doi.org/10.4137/GEG.S14176
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spelling doaj-cec5473cd2494df9aa669dae85d496ee2020-11-24T21:09:08ZengSAGE PublishingGenetics and Epigenetics1179-237X2014-01-01610.4137/GEG.S14176Bioinformatic Dissecting of TP53 Regulation Pathway Underlying Butyrate-induced Histone Modification in Epigenetic RegulationCong-Jun Li0Robert W. Li1Bovine Functional Genomics Laboratory, Agricultural Research Service, USDA. Beltsville, MD, USA.Bovine Functional Genomics Laboratory, Agricultural Research Service, USDA. Beltsville, MD, USA.Butyrate affects cell proliferation, differentiation, and motility. Butyrate inhibits histone deacetylase (HDAC) activities and induces cell-cycle arrest and apoptosis. TP53 is one of the most active upstream regulators discovered by ingenuity pathways analysis (IPA) in our RNA-sequencing data set. TP53 signaling pathway plays key role in many cellular processes. TP53 pathway and their involvement in cellular functions modified by butyrate treatment were scrutinized in this report by data mining the RNA-sequencing data using IPA (Ingenuity System ® ). The TP53 mechanistic pathway targets more than 600 genes. Downstream analysis predicted the activation of the TP53 pathway after butyrate treatment. The data mining also revealed that nine transcription factors are downstream regulators in TP53 signaling pathways. The analysis results also indicated that butyrate not only inhibits the HDAC activities, but also regulates genes encoding the HDAC enzymes through modification of histones and epigenomic landscape.https://doi.org/10.4137/GEG.S14176
collection DOAJ
language English
format Article
sources DOAJ
author Cong-Jun Li
Robert W. Li
spellingShingle Cong-Jun Li
Robert W. Li
Bioinformatic Dissecting of TP53 Regulation Pathway Underlying Butyrate-induced Histone Modification in Epigenetic Regulation
Genetics and Epigenetics
author_facet Cong-Jun Li
Robert W. Li
author_sort Cong-Jun Li
title Bioinformatic Dissecting of TP53 Regulation Pathway Underlying Butyrate-induced Histone Modification in Epigenetic Regulation
title_short Bioinformatic Dissecting of TP53 Regulation Pathway Underlying Butyrate-induced Histone Modification in Epigenetic Regulation
title_full Bioinformatic Dissecting of TP53 Regulation Pathway Underlying Butyrate-induced Histone Modification in Epigenetic Regulation
title_fullStr Bioinformatic Dissecting of TP53 Regulation Pathway Underlying Butyrate-induced Histone Modification in Epigenetic Regulation
title_full_unstemmed Bioinformatic Dissecting of TP53 Regulation Pathway Underlying Butyrate-induced Histone Modification in Epigenetic Regulation
title_sort bioinformatic dissecting of tp53 regulation pathway underlying butyrate-induced histone modification in epigenetic regulation
publisher SAGE Publishing
series Genetics and Epigenetics
issn 1179-237X
publishDate 2014-01-01
description Butyrate affects cell proliferation, differentiation, and motility. Butyrate inhibits histone deacetylase (HDAC) activities and induces cell-cycle arrest and apoptosis. TP53 is one of the most active upstream regulators discovered by ingenuity pathways analysis (IPA) in our RNA-sequencing data set. TP53 signaling pathway plays key role in many cellular processes. TP53 pathway and their involvement in cellular functions modified by butyrate treatment were scrutinized in this report by data mining the RNA-sequencing data using IPA (Ingenuity System ® ). The TP53 mechanistic pathway targets more than 600 genes. Downstream analysis predicted the activation of the TP53 pathway after butyrate treatment. The data mining also revealed that nine transcription factors are downstream regulators in TP53 signaling pathways. The analysis results also indicated that butyrate not only inhibits the HDAC activities, but also regulates genes encoding the HDAC enzymes through modification of histones and epigenomic landscape.
url https://doi.org/10.4137/GEG.S14176
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