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How to Build Transcriptional Network Models of Mammalian Pattern Formation

BACKGROUND: Genetic regulatory networks of sequence specific transcription factors underlie pattern formation in multicellular organisms. Deciphering and representing the mammalian networks is a central problem in development, neurobiology, and regenerative medicine. Transcriptional networks specify...

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Autores principales: Kioussi, Chrissa, Gross, Michael K.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527684/
https://www.ncbi.nlm.nih.gov/pubmed/18769640
http://dx.doi.org/10.1371/journal.pone.0002179
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author Kioussi, Chrissa
Gross, Michael K.
author_facet Kioussi, Chrissa
Gross, Michael K.
author_sort Kioussi, Chrissa
collection PubMed
description BACKGROUND: Genetic regulatory networks of sequence specific transcription factors underlie pattern formation in multicellular organisms. Deciphering and representing the mammalian networks is a central problem in development, neurobiology, and regenerative medicine. Transcriptional networks specify intermingled embryonic cell populations during pattern formation in the vertebrate neural tube. Each embryonic population gives rise to a distinct type of adult neuron. The homeodomain transcription factor Lbx1 is expressed in five such populations and loss of Lbx1 leads to distinct respecifications in each of the five populations. METHODOLOGY/PRINCIPAL FINDINGS: We have purified normal and respecified pools of these five populations from embryos bearing one or two copies of the null Lbx1(GFP) allele, respectively. Microarrays were used to show that expression levels of 8% of all transcription factor genes were altered in the respecified pool. These transcription factor genes constitute 20–30% of the active nodes of the transcriptional network that governs neural tube patterning. Half of the 141 regulated nodes were located in the top 150 clusters of ultraconserved non-coding regions. Generally, Lbx1 repressed genes that have expression patterns outside of the Lbx1-expressing domain and activated genes that have expression patterns inside the Lbx1-expressing domain. CONCLUSIONS/SIGNIFICANCE: Constraining epistasis analysis of Lbx1 to only those cells that normally express Lbx1 allowed unprecedented sensitivity in identifying Lbx1 network interactions and allowed the interactions to be assigned to a specific set of cell populations. We call this method ANCEA, or active node constrained epistasis analysis, and think that it will be generally useful in discovering and assigning network interactions to specific populations. We discuss how ANCEA, coupled with population partitioning analysis, can greatly facilitate the systematic dissection of transcriptional networks that underlie mammalian patterning.
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spelling pubmed-25276842008-09-02 How to Build Transcriptional Network Models of Mammalian Pattern Formation Kioussi, Chrissa Gross, Michael K. PLoS One Research Article BACKGROUND: Genetic regulatory networks of sequence specific transcription factors underlie pattern formation in multicellular organisms. Deciphering and representing the mammalian networks is a central problem in development, neurobiology, and regenerative medicine. Transcriptional networks specify intermingled embryonic cell populations during pattern formation in the vertebrate neural tube. Each embryonic population gives rise to a distinct type of adult neuron. The homeodomain transcription factor Lbx1 is expressed in five such populations and loss of Lbx1 leads to distinct respecifications in each of the five populations. METHODOLOGY/PRINCIPAL FINDINGS: We have purified normal and respecified pools of these five populations from embryos bearing one or two copies of the null Lbx1(GFP) allele, respectively. Microarrays were used to show that expression levels of 8% of all transcription factor genes were altered in the respecified pool. These transcription factor genes constitute 20–30% of the active nodes of the transcriptional network that governs neural tube patterning. Half of the 141 regulated nodes were located in the top 150 clusters of ultraconserved non-coding regions. Generally, Lbx1 repressed genes that have expression patterns outside of the Lbx1-expressing domain and activated genes that have expression patterns inside the Lbx1-expressing domain. CONCLUSIONS/SIGNIFICANCE: Constraining epistasis analysis of Lbx1 to only those cells that normally express Lbx1 allowed unprecedented sensitivity in identifying Lbx1 network interactions and allowed the interactions to be assigned to a specific set of cell populations. We call this method ANCEA, or active node constrained epistasis analysis, and think that it will be generally useful in discovering and assigning network interactions to specific populations. We discuss how ANCEA, coupled with population partitioning analysis, can greatly facilitate the systematic dissection of transcriptional networks that underlie mammalian patterning. Public Library of Science 2008-05-14 /pmc/articles/PMC2527684/ /pubmed/18769640 http://dx.doi.org/10.1371/journal.pone.0002179 Text en Kioussi, Gross. 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
Kioussi, Chrissa
Gross, Michael K.
How to Build Transcriptional Network Models of Mammalian Pattern Formation
title How to Build Transcriptional Network Models of Mammalian Pattern Formation
title_full How to Build Transcriptional Network Models of Mammalian Pattern Formation
title_fullStr How to Build Transcriptional Network Models of Mammalian Pattern Formation
title_full_unstemmed How to Build Transcriptional Network Models of Mammalian Pattern Formation
title_short How to Build Transcriptional Network Models of Mammalian Pattern Formation
title_sort how to build transcriptional network models of mammalian pattern formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527684/
https://www.ncbi.nlm.nih.gov/pubmed/18769640
http://dx.doi.org/10.1371/journal.pone.0002179
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