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Regulatory module network of basic/helix-loop-helix transcription factors in mouse brain
BACKGROUND: The basic/helix-loop-helix (bHLH) proteins are important components of the transcriptional regulatory network, controlling a variety of biological processes, especially the development of the central nervous system. Until now, reports describing the regulatory network of the bHLH transcr...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2258200/ https://www.ncbi.nlm.nih.gov/pubmed/18021424 http://dx.doi.org/10.1186/gb-2007-8-11-r244 |
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author | Li, Jing Liu, Zijing J Pan, Yuchun C Liu, Qi Fu, Xing Cooper, Nigel GF Li, Yixue Qiu, Mengsheng Shi, Tieliu |
author_facet | Li, Jing Liu, Zijing J Pan, Yuchun C Liu, Qi Fu, Xing Cooper, Nigel GF Li, Yixue Qiu, Mengsheng Shi, Tieliu |
author_sort | Li, Jing |
collection | PubMed |
description | BACKGROUND: The basic/helix-loop-helix (bHLH) proteins are important components of the transcriptional regulatory network, controlling a variety of biological processes, especially the development of the central nervous system. Until now, reports describing the regulatory network of the bHLH transcription factor (TF) family have been scarce. In order to understand the regulatory mechanisms of bHLH TFs in mouse brain, we inferred their regulatory network from genome-wide gene expression profiles with the module networks method. RESULTS: A regulatory network comprising 15 important bHLH TFs and 153 target genes was constructed. The network was divided into 28 modules based on expression profiles. A regulatory-motif search shows the complexity and diversity of the network. In addition, 26 cooperative bHLH TF pairs were also detected in the network. This cooperation suggests possible physical interactions or genetic regulation between TFs. Interestingly, some TFs in the network regulate more than one module. A novel cross-repression between Neurod6 and Hey2 was identified, which may control various functions in different brain regions. The presence of TF binding sites (TFBSs) in the promoter regions of their target genes validates more than 70% of TF-target gene pairs of the network. Literature mining provides additional support for five modules. More importantly, the regulatory relationships among selected key components are all validated in mutant mice. CONCLUSION: Our network is reliable and very informative for understanding the role of bHLH TFs in mouse brain development and function. It provides a framework for future experimental analyses. |
format | Text |
id | pubmed-2258200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22582002008-02-28 Regulatory module network of basic/helix-loop-helix transcription factors in mouse brain Li, Jing Liu, Zijing J Pan, Yuchun C Liu, Qi Fu, Xing Cooper, Nigel GF Li, Yixue Qiu, Mengsheng Shi, Tieliu Genome Biol Research BACKGROUND: The basic/helix-loop-helix (bHLH) proteins are important components of the transcriptional regulatory network, controlling a variety of biological processes, especially the development of the central nervous system. Until now, reports describing the regulatory network of the bHLH transcription factor (TF) family have been scarce. In order to understand the regulatory mechanisms of bHLH TFs in mouse brain, we inferred their regulatory network from genome-wide gene expression profiles with the module networks method. RESULTS: A regulatory network comprising 15 important bHLH TFs and 153 target genes was constructed. The network was divided into 28 modules based on expression profiles. A regulatory-motif search shows the complexity and diversity of the network. In addition, 26 cooperative bHLH TF pairs were also detected in the network. This cooperation suggests possible physical interactions or genetic regulation between TFs. Interestingly, some TFs in the network regulate more than one module. A novel cross-repression between Neurod6 and Hey2 was identified, which may control various functions in different brain regions. The presence of TF binding sites (TFBSs) in the promoter regions of their target genes validates more than 70% of TF-target gene pairs of the network. Literature mining provides additional support for five modules. More importantly, the regulatory relationships among selected key components are all validated in mutant mice. CONCLUSION: Our network is reliable and very informative for understanding the role of bHLH TFs in mouse brain development and function. It provides a framework for future experimental analyses. BioMed Central 2007 2007-11-19 /pmc/articles/PMC2258200/ /pubmed/18021424 http://dx.doi.org/10.1186/gb-2007-8-11-r244 Text en Copyright © 2007 Li et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Li, Jing Liu, Zijing J Pan, Yuchun C Liu, Qi Fu, Xing Cooper, Nigel GF Li, Yixue Qiu, Mengsheng Shi, Tieliu Regulatory module network of basic/helix-loop-helix transcription factors in mouse brain |
title | Regulatory module network of basic/helix-loop-helix transcription factors in mouse brain |
title_full | Regulatory module network of basic/helix-loop-helix transcription factors in mouse brain |
title_fullStr | Regulatory module network of basic/helix-loop-helix transcription factors in mouse brain |
title_full_unstemmed | Regulatory module network of basic/helix-loop-helix transcription factors in mouse brain |
title_short | Regulatory module network of basic/helix-loop-helix transcription factors in mouse brain |
title_sort | regulatory module network of basic/helix-loop-helix transcription factors in mouse brain |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2258200/ https://www.ncbi.nlm.nih.gov/pubmed/18021424 http://dx.doi.org/10.1186/gb-2007-8-11-r244 |
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