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Dynamics of Posttranslational Modifications of p53
The latest experimental evidence indicates that acetylation of p53 at K164 (lysine 164) and K120 may induce directly cell apoptosis under severe DNA damage. However, previous cell apoptosis models only studied the effects of active and/or inactive p53, that is, phosphorylation/dephosphorylation of p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037116/ https://www.ncbi.nlm.nih.gov/pubmed/24899917 http://dx.doi.org/10.1155/2014/245610 |
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author | Fan, Qing-Duan Wu, Guang Liu, Zeng-Rong |
author_facet | Fan, Qing-Duan Wu, Guang Liu, Zeng-Rong |
author_sort | Fan, Qing-Duan |
collection | PubMed |
description | The latest experimental evidence indicates that acetylation of p53 at K164 (lysine 164) and K120 may induce directly cell apoptosis under severe DNA damage. However, previous cell apoptosis models only studied the effects of active and/or inactive p53, that is, phosphorylation/dephosphorylation of p53. In the present paper, based partly on Geva-Zatorsky et al. (2006) and Batchelor et al. (2008), we propose a new cell apoptosis network, in which p53 has three statuses, that is, unphosphorylated p53, phosphorylated p53, and acetylated p53. The time delay differential equations (DDEs) are formulated based on our network to investigate the dynamical insights of p53-induced cell apoptosis. In agreement with experiments (Loewer et al. (2010)), our simulations indicate that acetylated p53 accumulates gradually and then induces the proapoptotic protein Bax under enough DNA damage. Moreover, phosphorylated p53 oscillates and initiates cell repair during DNA damage. |
format | Online Article Text |
id | pubmed-4037116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40371162014-06-04 Dynamics of Posttranslational Modifications of p53 Fan, Qing-Duan Wu, Guang Liu, Zeng-Rong Comput Math Methods Med Research Article The latest experimental evidence indicates that acetylation of p53 at K164 (lysine 164) and K120 may induce directly cell apoptosis under severe DNA damage. However, previous cell apoptosis models only studied the effects of active and/or inactive p53, that is, phosphorylation/dephosphorylation of p53. In the present paper, based partly on Geva-Zatorsky et al. (2006) and Batchelor et al. (2008), we propose a new cell apoptosis network, in which p53 has three statuses, that is, unphosphorylated p53, phosphorylated p53, and acetylated p53. The time delay differential equations (DDEs) are formulated based on our network to investigate the dynamical insights of p53-induced cell apoptosis. In agreement with experiments (Loewer et al. (2010)), our simulations indicate that acetylated p53 accumulates gradually and then induces the proapoptotic protein Bax under enough DNA damage. Moreover, phosphorylated p53 oscillates and initiates cell repair during DNA damage. Hindawi Publishing Corporation 2014 2014-05-12 /pmc/articles/PMC4037116/ /pubmed/24899917 http://dx.doi.org/10.1155/2014/245610 Text en Copyright © 2014 Qing-Duan Fan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Fan, Qing-Duan Wu, Guang Liu, Zeng-Rong Dynamics of Posttranslational Modifications of p53 |
title | Dynamics of Posttranslational Modifications of p53 |
title_full | Dynamics of Posttranslational Modifications of p53 |
title_fullStr | Dynamics of Posttranslational Modifications of p53 |
title_full_unstemmed | Dynamics of Posttranslational Modifications of p53 |
title_short | Dynamics of Posttranslational Modifications of p53 |
title_sort | dynamics of posttranslational modifications of p53 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037116/ https://www.ncbi.nlm.nih.gov/pubmed/24899917 http://dx.doi.org/10.1155/2014/245610 |
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