The dynamics of stress p53-Mdm2 network regulated by p300 and HDAC1.

We construct a stress p53-Mdm2-p300-HDAC1 regulatory network that is activated and stabilised by two regulatory proteins, p300 and HDAC1. Different activation levels of [Formula: see text] observed due to these regulators during stress condition have been investigated using a deterministic as well a...

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Main Authors: Akshit Arora, Saurav Gera, Tanuj Maheshwari, Dhwani Raghav, Md Jahoor Alam, R K Brojen Singh, Subhash M Agarwal
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3577848?pdf=render
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spelling doaj-b4b5a54d627b4b078ed95e3045fbfa3d2020-11-24T21:43:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0182e5273610.1371/journal.pone.0052736The dynamics of stress p53-Mdm2 network regulated by p300 and HDAC1.Akshit AroraSaurav GeraTanuj MaheshwariDhwani RaghavMd Jahoor AlamR K Brojen SinghSubhash M AgarwalWe construct a stress p53-Mdm2-p300-HDAC1 regulatory network that is activated and stabilised by two regulatory proteins, p300 and HDAC1. Different activation levels of [Formula: see text] observed due to these regulators during stress condition have been investigated using a deterministic as well as a stochastic approach to understand how the cell responds during stress conditions. We found that these regulators help in adjusting p53 to different conditions as identified by various oscillatory states, namely fixed point oscillations, damped oscillations and sustain oscillations. On assessing the impact of p300 on p53-Mdm2 network we identified three states: first stabilised or normal condition where the impact of p300 is negligible, second an interim region where p53 is activated due to interaction between p53 and p300, and finally the third regime where excess of p300 leads to cell stress condition. Similarly evaluation of HDAC1 on our model led to identification of the above three distinct states. Also we observe that noise in stochastic cellular system helps to reach each oscillatory state quicker than those in deterministic case. The constructed model validated different experimental findings qualitatively.http://europepmc.org/articles/PMC3577848?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Akshit Arora
Saurav Gera
Tanuj Maheshwari
Dhwani Raghav
Md Jahoor Alam
R K Brojen Singh
Subhash M Agarwal
spellingShingle Akshit Arora
Saurav Gera
Tanuj Maheshwari
Dhwani Raghav
Md Jahoor Alam
R K Brojen Singh
Subhash M Agarwal
The dynamics of stress p53-Mdm2 network regulated by p300 and HDAC1.
PLoS ONE
author_facet Akshit Arora
Saurav Gera
Tanuj Maheshwari
Dhwani Raghav
Md Jahoor Alam
R K Brojen Singh
Subhash M Agarwal
author_sort Akshit Arora
title The dynamics of stress p53-Mdm2 network regulated by p300 and HDAC1.
title_short The dynamics of stress p53-Mdm2 network regulated by p300 and HDAC1.
title_full The dynamics of stress p53-Mdm2 network regulated by p300 and HDAC1.
title_fullStr The dynamics of stress p53-Mdm2 network regulated by p300 and HDAC1.
title_full_unstemmed The dynamics of stress p53-Mdm2 network regulated by p300 and HDAC1.
title_sort dynamics of stress p53-mdm2 network regulated by p300 and hdac1.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description We construct a stress p53-Mdm2-p300-HDAC1 regulatory network that is activated and stabilised by two regulatory proteins, p300 and HDAC1. Different activation levels of [Formula: see text] observed due to these regulators during stress condition have been investigated using a deterministic as well as a stochastic approach to understand how the cell responds during stress conditions. We found that these regulators help in adjusting p53 to different conditions as identified by various oscillatory states, namely fixed point oscillations, damped oscillations and sustain oscillations. On assessing the impact of p300 on p53-Mdm2 network we identified three states: first stabilised or normal condition where the impact of p300 is negligible, second an interim region where p53 is activated due to interaction between p53 and p300, and finally the third regime where excess of p300 leads to cell stress condition. Similarly evaluation of HDAC1 on our model led to identification of the above three distinct states. Also we observe that noise in stochastic cellular system helps to reach each oscillatory state quicker than those in deterministic case. The constructed model validated different experimental findings qualitatively.
url http://europepmc.org/articles/PMC3577848?pdf=render
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