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Towards a quantitative understanding of the MITF-PIAS3-STAT3 connection
BACKGROUND: Expression of the two transcription factors microphthalmia-associated transcription factor (MITF) and signal transducer and activator of transcription 3 (STAT3) are tightly connected to cell proliferation and survival, and are important for melanocyte development. The co-regulation of MI...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341200/ https://www.ncbi.nlm.nih.gov/pubmed/22316093 http://dx.doi.org/10.1186/1752-0509-6-11 |
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author | Thingnes, Josef Lavelle, Timothy J Gjuvsland, Arne B Omholt, Stig W Hovig, Eivind |
author_facet | Thingnes, Josef Lavelle, Timothy J Gjuvsland, Arne B Omholt, Stig W Hovig, Eivind |
author_sort | Thingnes, Josef |
collection | PubMed |
description | BACKGROUND: Expression of the two transcription factors microphthalmia-associated transcription factor (MITF) and signal transducer and activator of transcription 3 (STAT3) are tightly connected to cell proliferation and survival, and are important for melanocyte development. The co-regulation of MITF and STAT3 via their binding to a common inhibitor Protein Inhibitor of Activated STAT3 (PIAS3) is intriguing. A better quantitative understanding of this regulation is likely to be important for elucidation of the melanocyte biology. RESULTS: We present a mathematical model describing the MITF-PIAS3-STAT3 signalling network. A default parameter set was developed, partly informed by the literature and partly by constraining the model to mimic reported behavioural features of the system. In addition, a set of experiment-specific parameters was derived for each of 28 experiments reported in the literature. The model seems capable of accounting for most of these experiments in terms of observed temporal development of protein amounts and phosphorylation states. Further, the results also suggest that this system possesses some regulatory features yet to be elucidated. CONCLUSIONS: We find that the experimentally observed crosstalk between MITF and STAT3 via PIAS3 in melanocytes is faithfully reproduced in our model, offering mechanistic explanations for this behaviour, as well as providing a scaffold for further studies of MITF signalling in melanoma. |
format | Online Article Text |
id | pubmed-3341200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33412002012-05-02 Towards a quantitative understanding of the MITF-PIAS3-STAT3 connection Thingnes, Josef Lavelle, Timothy J Gjuvsland, Arne B Omholt, Stig W Hovig, Eivind BMC Syst Biol Research Article BACKGROUND: Expression of the two transcription factors microphthalmia-associated transcription factor (MITF) and signal transducer and activator of transcription 3 (STAT3) are tightly connected to cell proliferation and survival, and are important for melanocyte development. The co-regulation of MITF and STAT3 via their binding to a common inhibitor Protein Inhibitor of Activated STAT3 (PIAS3) is intriguing. A better quantitative understanding of this regulation is likely to be important for elucidation of the melanocyte biology. RESULTS: We present a mathematical model describing the MITF-PIAS3-STAT3 signalling network. A default parameter set was developed, partly informed by the literature and partly by constraining the model to mimic reported behavioural features of the system. In addition, a set of experiment-specific parameters was derived for each of 28 experiments reported in the literature. The model seems capable of accounting for most of these experiments in terms of observed temporal development of protein amounts and phosphorylation states. Further, the results also suggest that this system possesses some regulatory features yet to be elucidated. CONCLUSIONS: We find that the experimentally observed crosstalk between MITF and STAT3 via PIAS3 in melanocytes is faithfully reproduced in our model, offering mechanistic explanations for this behaviour, as well as providing a scaffold for further studies of MITF signalling in melanoma. BioMed Central 2012-02-08 /pmc/articles/PMC3341200/ /pubmed/22316093 http://dx.doi.org/10.1186/1752-0509-6-11 Text en Copyright ©2012 Thingnes et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Thingnes, Josef Lavelle, Timothy J Gjuvsland, Arne B Omholt, Stig W Hovig, Eivind Towards a quantitative understanding of the MITF-PIAS3-STAT3 connection |
title | Towards a quantitative understanding of the MITF-PIAS3-STAT3 connection |
title_full | Towards a quantitative understanding of the MITF-PIAS3-STAT3 connection |
title_fullStr | Towards a quantitative understanding of the MITF-PIAS3-STAT3 connection |
title_full_unstemmed | Towards a quantitative understanding of the MITF-PIAS3-STAT3 connection |
title_short | Towards a quantitative understanding of the MITF-PIAS3-STAT3 connection |
title_sort | towards a quantitative understanding of the mitf-pias3-stat3 connection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341200/ https://www.ncbi.nlm.nih.gov/pubmed/22316093 http://dx.doi.org/10.1186/1752-0509-6-11 |
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