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A New Perspective on Transcriptional System Regulation

It has been hypothesized that the net expression of a gene is determined by the combined effects of various transcriptional system regulators (TSRs). However, characterizing the complexity of regulation of the transcriptome is a major challenge. Principal component analysis on 17,550 heterogeneous h...

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Published in:PloS one 2008-02, Vol.3 (2), p.e1656
Main Authors: Fehrmann, Rudolf S. N, de Jonge, Hendrik J. M, ter Elst, Arja, de Vries, André, Crijns, Anne G. P, Weidenaar, Alida C, Gerbens, Frans, de Jong, Steven, van der Zee, Ate G. J, de Vries, Elisabeth G. E, Kamps, Willem A, Hofstra, Robert M. W, te Meerman, Gerard J, de Bont, Eveline S. J. M
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creator Fehrmann, Rudolf S. N
de Jonge, Hendrik J. M
ter Elst, Arja
de Vries, André
Crijns, Anne G. P
Weidenaar, Alida C
Gerbens, Frans
de Jong, Steven
van der Zee, Ate G. J
de Vries, Elisabeth G. E
Kamps, Willem A
Hofstra, Robert M. W
te Meerman, Gerard J
de Bont, Eveline S. J. M
description It has been hypothesized that the net expression of a gene is determined by the combined effects of various transcriptional system regulators (TSRs). However, characterizing the complexity of regulation of the transcriptome is a major challenge. Principal component analysis on 17,550 heterogeneous human microarray experiments revealed that 50 orthogonal factors (hereafter called TSRs) are able to capture 64% of the variability in expression in a wide range of experimental conditions and tissues. We identified gene clusters controlled in the same direction and show that gene expression can be conceptualized as a process influenced by a fairly limited set of TSRs. Furthermore, TSRs can be linked to biological functions, as we demonstrate a strong relation between TSR-related gene clusters and biological functionality as well as cellular localization, i.e. gene products of similarly regulated genes by a specific TSR are located in identical parts of a cell. Using 3,934 diverse mouse microarray experiments we found striking similarities in transcriptional system regulation between human and mouse. Our results give biological insights into regulation of the cellular transcriptome and provide a tool to characterize expression profiles with highly reliable TSRs instead of thousands of individual genes, leading to a >500-fold reduction of complexity with just 50 TSRs. This might open new avenues for those performing gene expression profiling studies.
doi_str_mv 10.1371/journal.pone.0001656
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subjects Analysis
Animal experimentation
Genes
Genetic aspects
Genetic research
Transcription (Genetics)
title A New Perspective on Transcriptional System Regulation
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