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Seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes
BACKGROUND: The identification of polymorphisms and/or genes responsible for an organism's radiosensitivity increases the knowledge about the cell cycle and the mechanism of the phenomena themselves, possibly providing the researchers with a better understanding of the process of carcinogenesis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108879/ https://www.ncbi.nlm.nih.gov/pubmed/25079915 http://dx.doi.org/10.1186/1742-4682-11-S1-S2 |
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author | Zyla, Joanna Finnon, Paul Bulman, Robert Bouffler, Simon Badie, Christophe Polanska, Joanna |
author_facet | Zyla, Joanna Finnon, Paul Bulman, Robert Bouffler, Simon Badie, Christophe Polanska, Joanna |
author_sort | Zyla, Joanna |
collection | PubMed |
description | BACKGROUND: The identification of polymorphisms and/or genes responsible for an organism's radiosensitivity increases the knowledge about the cell cycle and the mechanism of the phenomena themselves, possibly providing the researchers with a better understanding of the process of carcinogenesis. AIM: The aim of the study was to develop a data analysis strategy capable of discovering the genetic background of radiosensitivity in the case of small sample size studies. RESULTS: Among many indirect measures of radiosensitivity known, the level of radiation-induced chromosomal aberrations was used in the study. Mathematical modelling allowed the transformation of the yield-time curve of radiation-induced chromosomal aberrations into the exponential curve with limited number of parameters, while Gaussian mixture models applied to the distributions of these parameters provided the criteria for mouse strain classification. A detailed comparative analysis of genotypes between the obtained subpopulations of mice followed by functional validation provided a set of candidate polymorphisms that might be related to radiosensitivity. Among 1857 candidate relevant SNPs, that cluster in 28 genes, eight SNPs were detected nonsynonymous (nsSNP) on protein function. Two of them, rs48840878 (gene Msh3) and rs5144199 (gene Cc2d2a), were predicted as having increased probability of a deleterious effect. Additionally, rs48840878 is capable of disordering phosphorylation with 14 PKs. In silico analysis of candidate relevant SNP similarity score distribution among 60 CGD mouse strains allowed for the identification of SEA/GnJ and ZALENDE/EiJ mouse strains (95.26% and 86.53% genetic consistency respectively) as the most similar to radiosensitive subpopulation CONCLUSIONS: A complete step-by-step strategy for seeking the genetic signature of radiosensitivity in the case of small sample size studies conducted on mouse models was proposed. It is shown that the strategy, which is a combination of mathematical modelling, statistical analysis and data mining methodology, allows for the discovery of candidate polymorphisms which might be responsible for radiosensitivity phenomena. |
format | Online Article Text |
id | pubmed-4108879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41088792014-08-04 Seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes Zyla, Joanna Finnon, Paul Bulman, Robert Bouffler, Simon Badie, Christophe Polanska, Joanna Theor Biol Med Model Research BACKGROUND: The identification of polymorphisms and/or genes responsible for an organism's radiosensitivity increases the knowledge about the cell cycle and the mechanism of the phenomena themselves, possibly providing the researchers with a better understanding of the process of carcinogenesis. AIM: The aim of the study was to develop a data analysis strategy capable of discovering the genetic background of radiosensitivity in the case of small sample size studies. RESULTS: Among many indirect measures of radiosensitivity known, the level of radiation-induced chromosomal aberrations was used in the study. Mathematical modelling allowed the transformation of the yield-time curve of radiation-induced chromosomal aberrations into the exponential curve with limited number of parameters, while Gaussian mixture models applied to the distributions of these parameters provided the criteria for mouse strain classification. A detailed comparative analysis of genotypes between the obtained subpopulations of mice followed by functional validation provided a set of candidate polymorphisms that might be related to radiosensitivity. Among 1857 candidate relevant SNPs, that cluster in 28 genes, eight SNPs were detected nonsynonymous (nsSNP) on protein function. Two of them, rs48840878 (gene Msh3) and rs5144199 (gene Cc2d2a), were predicted as having increased probability of a deleterious effect. Additionally, rs48840878 is capable of disordering phosphorylation with 14 PKs. In silico analysis of candidate relevant SNP similarity score distribution among 60 CGD mouse strains allowed for the identification of SEA/GnJ and ZALENDE/EiJ mouse strains (95.26% and 86.53% genetic consistency respectively) as the most similar to radiosensitive subpopulation CONCLUSIONS: A complete step-by-step strategy for seeking the genetic signature of radiosensitivity in the case of small sample size studies conducted on mouse models was proposed. It is shown that the strategy, which is a combination of mathematical modelling, statistical analysis and data mining methodology, allows for the discovery of candidate polymorphisms which might be responsible for radiosensitivity phenomena. BioMed Central 2014-05-07 /pmc/articles/PMC4108879/ /pubmed/25079915 http://dx.doi.org/10.1186/1742-4682-11-S1-S2 Text en Copyright © 2014 Zyla 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zyla, Joanna Finnon, Paul Bulman, Robert Bouffler, Simon Badie, Christophe Polanska, Joanna Seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes |
title | Seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes |
title_full | Seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes |
title_fullStr | Seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes |
title_full_unstemmed | Seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes |
title_short | Seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes |
title_sort | seeking genetic signature of radiosensitivity - a novel method for data analysis in case of small sample sizes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108879/ https://www.ncbi.nlm.nih.gov/pubmed/25079915 http://dx.doi.org/10.1186/1742-4682-11-S1-S2 |
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