Modeling and Experimental Methods to Probe the Link between Global Transcription and Spatial Organization of Chromosomes
Author(s) -
K. Venkatesan Iyer,
Shovamayee Maharana,
Soumya Gupta,
Albert Libchaber,
Tsvi Tlusty,
G. V. Shivashankar
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0046628
Subject(s) - transcription factor , chromosome conformation capture , biology , chromosome , interphase , gene , gene regulatory network , genetics , transcription (linguistics) , genomic organization , spatial organization , nucleus , regulation of gene expression , gene expression , genome , computational biology , topology (electrical circuits) , microbiology and biotechnology , enhancer , evolutionary biology , combinatorics , philosophy , linguistics , mathematics
Genomes are spatially assembled into chromosome territories (CT) within the nucleus of living cells. Recent evidences have suggested associations between three-dimensional organization of CTs and the active gene clusters within neighboring CTs. These gene clusters are part of signaling networks sharing similar transcription factor or other downstream transcription machineries. Hence, presence of such gene clusters of active signaling networks in a cell type may regulate the spatial organization of chromosomes in the nucleus. However, given the probabilistic nature of chromosome positions and complex transcription factor networks (TFNs), quantitative methods to establish their correlation is lacking. In this paper, we use chromosome positions and gene expression profiles in interphase fibroblasts and describe methods to capture the correspondence between their spatial position and expression. In addition, numerical simulations designed to incorporate the interacting TFNs, reveal that the chromosome positions are also optimized for the activity of these networks. These methods were validated for specific chromosome pairs mapped in two distinct transcriptional states of T-Cells (naïve and activated). Taken together, our methods highlight the functional coupling between topology of chromosomes and their respective gene expression patterns.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom