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Predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals

BACKGROUND: The expression of gene batteries, genomic units of functionally linked genes which are activated by similar sets of cis- and trans-acting regulators, has been proposed as a major determinant of cell specialization in metazoans. We developed a predictive procedure to screen the mouse and...

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Autores principales: Nelander, Sven, Larsson, Erik, Kristiansson, Erik, Månsson, Robert, Nerman, Olle, Sigvardsson, Mikael, Mostad, Petter, Lindahl, Per
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1134656/
https://www.ncbi.nlm.nih.gov/pubmed/15882449
http://dx.doi.org/10.1186/1471-2164-6-68
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author Nelander, Sven
Larsson, Erik
Kristiansson, Erik
Månsson, Robert
Nerman, Olle
Sigvardsson, Mikael
Mostad, Petter
Lindahl, Per
author_facet Nelander, Sven
Larsson, Erik
Kristiansson, Erik
Månsson, Robert
Nerman, Olle
Sigvardsson, Mikael
Mostad, Petter
Lindahl, Per
author_sort Nelander, Sven
collection PubMed
description BACKGROUND: The expression of gene batteries, genomic units of functionally linked genes which are activated by similar sets of cis- and trans-acting regulators, has been proposed as a major determinant of cell specialization in metazoans. We developed a predictive procedure to screen the mouse and human genomes and transcriptomes for cases of gene-battery-like regulation. RESULTS: In a screen that covered ~40 per cent of all annotated protein-coding genes, we identified 21 co-expressed gene clusters with statistically supported sharing of cis-regulatory sequence elements. 66 predicted cases of over-represented transcription factor binding motifs were validated against the literature and fell into three categories: (i) previously described cases of gene battery-like regulation, (ii) previously unreported cases of gene battery-like regulation with some support in a limited number of genes, and (iii) predicted cases that currently lack experimental support. The novel predictions include for example Sox 17 and RFX transcription factor binding sites that were detected in ~10% of all testis specific genes, and HNF-1 and 4 binding sites that were detected in ~30% of all kidney specific genes respectively. The results are publicly available at . CONCLUSION: 21 co-expressed gene clusters were enriched for a total of 66 shared cis-regulatory sequence elements. A majority of these predictions represent novel cases of potential co-regulation of functionally coupled proteins. Critical technical parameters were evaluated, and the results and the methods provide a valuable resource for future experimental design.
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spelling pubmed-11346562005-05-21 Predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals Nelander, Sven Larsson, Erik Kristiansson, Erik Månsson, Robert Nerman, Olle Sigvardsson, Mikael Mostad, Petter Lindahl, Per BMC Genomics Research Article BACKGROUND: The expression of gene batteries, genomic units of functionally linked genes which are activated by similar sets of cis- and trans-acting regulators, has been proposed as a major determinant of cell specialization in metazoans. We developed a predictive procedure to screen the mouse and human genomes and transcriptomes for cases of gene-battery-like regulation. RESULTS: In a screen that covered ~40 per cent of all annotated protein-coding genes, we identified 21 co-expressed gene clusters with statistically supported sharing of cis-regulatory sequence elements. 66 predicted cases of over-represented transcription factor binding motifs were validated against the literature and fell into three categories: (i) previously described cases of gene battery-like regulation, (ii) previously unreported cases of gene battery-like regulation with some support in a limited number of genes, and (iii) predicted cases that currently lack experimental support. The novel predictions include for example Sox 17 and RFX transcription factor binding sites that were detected in ~10% of all testis specific genes, and HNF-1 and 4 binding sites that were detected in ~30% of all kidney specific genes respectively. The results are publicly available at . CONCLUSION: 21 co-expressed gene clusters were enriched for a total of 66 shared cis-regulatory sequence elements. A majority of these predictions represent novel cases of potential co-regulation of functionally coupled proteins. Critical technical parameters were evaluated, and the results and the methods provide a valuable resource for future experimental design. BioMed Central 2005-05-09 /pmc/articles/PMC1134656/ /pubmed/15882449 http://dx.doi.org/10.1186/1471-2164-6-68 Text en Copyright © 2005 Nelander 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 Article
Nelander, Sven
Larsson, Erik
Kristiansson, Erik
Månsson, Robert
Nerman, Olle
Sigvardsson, Mikael
Mostad, Petter
Lindahl, Per
Predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals
title Predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals
title_full Predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals
title_fullStr Predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals
title_full_unstemmed Predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals
title_short Predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals
title_sort predictive screening for regulators of conserved functional gene modules (gene batteries) in mammals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1134656/
https://www.ncbi.nlm.nih.gov/pubmed/15882449
http://dx.doi.org/10.1186/1471-2164-6-68
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