4.5 Article

Wide-scale alterations in interchromosomal organization in breast cancer cells: defining a network of interacting chromosomes

期刊

HUMAN MOLECULAR GENETICS
卷 23, 期 19, 页码 5133-5146

出版社

OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddu237

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资金

  1. National Instititutes of Health [GM-072131]
  2. National Science Foundation [IIS-0713489, IIS-1115220]
  3. University at Buffalo Foundation [9351115726]
  4. Div Of Information & Intelligent Systems
  5. Direct For Computer & Info Scie & Enginr [1115220] Funding Source: National Science Foundation

向作者/读者索取更多资源

The interchromosomal spatial positionings of a subset of human chromosomes was examined in the human breast cell line MCF10A (10A) and its malignant counterpart MCF10CA1a (CA1a). The nine chromosomes selected (#1, 4, 11, 12, 15, 16, 18, 21 and X) cover a wide range in size and gene density and compose 40% of the total human genome. Radial positioning of the chromosome territories (CT) was size dependent with certain of the CT more peripheral in CA1a. Each CT was in close proximity (interaction) with a similar number of other CT except the inactive CTXi. It had lower levels of interchromosomal partners in 10A which increased strikingly in CA1a. Major alterations from 10A to CA1a were detected in the pairwise interaction profiles which were subdivided into five types of altered interaction profiles: overall increase, overall decrease, switching from 1 to >2, vice versa or no change. A global data mining program termed the chromatic median calculated the most probable overall association network for the entire subset of CT. This interchromosomal network was drastically altered in CA1a with only 1 of 20 shared connections. We conclude that CT undergo multiple and preferred interactions with other CT in the cell nucleus and form preferred albeit probabilistic interchromosomal networks. This network of interactions is highly altered in malignant human breast cells. It is intriguing to consider the relationship of these alterations to the corresponding changes in the gene expression program of these malignant cancer cells.

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