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Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle

The interchromosomal organization of a subset of human chromosomes (#1, 4, 11, 12, 16, 17, and 18) was examined in G1 and S phase of human WI38 lung fibroblast and MCF10A breast epithelial cells. Radial positioning of the chromosome territories (CTs) was independent of gene density, but size depende...

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Autores principales: Fritz, Andrew J., Stojkovic, Branislav, Ding, Hu, Xu, Jinhui, Bhattacharya, Sambit, Berezney, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183423/
https://www.ncbi.nlm.nih.gov/pubmed/25275626
http://dx.doi.org/10.1371/journal.pcbi.1003857
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author Fritz, Andrew J.
Stojkovic, Branislav
Ding, Hu
Xu, Jinhui
Bhattacharya, Sambit
Berezney, Ronald
author_facet Fritz, Andrew J.
Stojkovic, Branislav
Ding, Hu
Xu, Jinhui
Bhattacharya, Sambit
Berezney, Ronald
author_sort Fritz, Andrew J.
collection PubMed
description The interchromosomal organization of a subset of human chromosomes (#1, 4, 11, 12, 16, 17, and 18) was examined in G1 and S phase of human WI38 lung fibroblast and MCF10A breast epithelial cells. Radial positioning of the chromosome territories (CTs) was independent of gene density, but size dependent. While no changes in radial positioning during the cell cycle were detected, there were stage-specific differences between cell types. Each CT was in close proximity (interaction) with a similar number of other CT except the gene rich CT17 which had significantly more interactions. Furthermore, CT17 was a member of the highest pairwise CT combinations with multiple interactions. Major differences were detected in the pairwise interaction profiles of MCF10A versus WI38 including cell cycle alterations from G1 to S. These alterations in interaction profiles were subdivided into five types: overall increase, overall decrease, switching from 1 to ≥2 interactions, vice versa, or no change. A global data mining program termed the chromatic median determined the most probable overall association network for the entire subset of CT. This probabilistic interchromosomal network was nearly completely different between the two cell lines. It was also strikingly altered across the cell cycle in MCF10A, but only slightly in WI38. We conclude that CT undergo multiple and preferred interactions with other CT in the nucleus and form preferred -albeit probabilistic- interchromosomal networks. This network of interactions is altered across the cell cycle and between cell types. It is intriguing to consider the relationship of these alterations to the corresponding changes in the gene expression program across the cell cycle and in different cell types.
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spelling pubmed-41834232014-10-07 Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle Fritz, Andrew J. Stojkovic, Branislav Ding, Hu Xu, Jinhui Bhattacharya, Sambit Berezney, Ronald PLoS Comput Biol Research Article The interchromosomal organization of a subset of human chromosomes (#1, 4, 11, 12, 16, 17, and 18) was examined in G1 and S phase of human WI38 lung fibroblast and MCF10A breast epithelial cells. Radial positioning of the chromosome territories (CTs) was independent of gene density, but size dependent. While no changes in radial positioning during the cell cycle were detected, there were stage-specific differences between cell types. Each CT was in close proximity (interaction) with a similar number of other CT except the gene rich CT17 which had significantly more interactions. Furthermore, CT17 was a member of the highest pairwise CT combinations with multiple interactions. Major differences were detected in the pairwise interaction profiles of MCF10A versus WI38 including cell cycle alterations from G1 to S. These alterations in interaction profiles were subdivided into five types: overall increase, overall decrease, switching from 1 to ≥2 interactions, vice versa, or no change. A global data mining program termed the chromatic median determined the most probable overall association network for the entire subset of CT. This probabilistic interchromosomal network was nearly completely different between the two cell lines. It was also strikingly altered across the cell cycle in MCF10A, but only slightly in WI38. We conclude that CT undergo multiple and preferred interactions with other CT in the nucleus and form preferred -albeit probabilistic- interchromosomal networks. This network of interactions is altered across the cell cycle and between cell types. It is intriguing to consider the relationship of these alterations to the corresponding changes in the gene expression program across the cell cycle and in different cell types. Public Library of Science 2014-10-02 /pmc/articles/PMC4183423/ /pubmed/25275626 http://dx.doi.org/10.1371/journal.pcbi.1003857 Text en © 2014 Fritz et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fritz, Andrew J.
Stojkovic, Branislav
Ding, Hu
Xu, Jinhui
Bhattacharya, Sambit
Berezney, Ronald
Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle
title Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle
title_full Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle
title_fullStr Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle
title_full_unstemmed Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle
title_short Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle
title_sort cell type specific alterations in interchromosomal networks across the cell cycle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183423/
https://www.ncbi.nlm.nih.gov/pubmed/25275626
http://dx.doi.org/10.1371/journal.pcbi.1003857
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