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Transcriptional Autoregulatory Loops Are Highly Conserved in Vertebrate Evolution
BACKGROUND: Feedback loops are the simplest building blocks of transcriptional regulatory networks and therefore their behavior in the course of evolution is of prime interest. METHODOLOGY: We address the question of enrichment of the number of autoregulatory feedback loops in higher organisms. Firs...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527657/ https://www.ncbi.nlm.nih.gov/pubmed/18791639 http://dx.doi.org/10.1371/journal.pone.0003210 |
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author | Kiełbasa, Szymon M. Vingron, Martin |
author_facet | Kiełbasa, Szymon M. Vingron, Martin |
author_sort | Kiełbasa, Szymon M. |
collection | PubMed |
description | BACKGROUND: Feedback loops are the simplest building blocks of transcriptional regulatory networks and therefore their behavior in the course of evolution is of prime interest. METHODOLOGY: We address the question of enrichment of the number of autoregulatory feedback loops in higher organisms. First, based on predicted autoregulatory binding sites we count the number of autoregulatory loops. We compare it to estimates obtained either by assuming that each (conserved) gene has the same chance to be a target of a given factor or by assuming that each conserved sequence position has an equal chance to be a binding site of the factor. CONCLUSIONS: We demonstrate that the numbers of putative autoregulatory loops conserved between human and fugu, danio or chicken are significantly higher than expected. Moreover we show, that conserved autoregulatory binding sites cluster close to the factors' starts of transcription. We conclude, that transcriptional autoregulatory feedback loops constitute a core transcriptional network motif and their conservation has been maintained in higher vertebrate organism evolution. |
format | Text |
id | pubmed-2527657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25276572008-09-15 Transcriptional Autoregulatory Loops Are Highly Conserved in Vertebrate Evolution Kiełbasa, Szymon M. Vingron, Martin PLoS One Research Article BACKGROUND: Feedback loops are the simplest building blocks of transcriptional regulatory networks and therefore their behavior in the course of evolution is of prime interest. METHODOLOGY: We address the question of enrichment of the number of autoregulatory feedback loops in higher organisms. First, based on predicted autoregulatory binding sites we count the number of autoregulatory loops. We compare it to estimates obtained either by assuming that each (conserved) gene has the same chance to be a target of a given factor or by assuming that each conserved sequence position has an equal chance to be a binding site of the factor. CONCLUSIONS: We demonstrate that the numbers of putative autoregulatory loops conserved between human and fugu, danio or chicken are significantly higher than expected. Moreover we show, that conserved autoregulatory binding sites cluster close to the factors' starts of transcription. We conclude, that transcriptional autoregulatory feedback loops constitute a core transcriptional network motif and their conservation has been maintained in higher vertebrate organism evolution. Public Library of Science 2008-09-15 /pmc/articles/PMC2527657/ /pubmed/18791639 http://dx.doi.org/10.1371/journal.pone.0003210 Text en Kiełbasa et al. 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 Kiełbasa, Szymon M. Vingron, Martin Transcriptional Autoregulatory Loops Are Highly Conserved in Vertebrate Evolution |
title | Transcriptional Autoregulatory Loops Are Highly Conserved in Vertebrate Evolution |
title_full | Transcriptional Autoregulatory Loops Are Highly Conserved in Vertebrate Evolution |
title_fullStr | Transcriptional Autoregulatory Loops Are Highly Conserved in Vertebrate Evolution |
title_full_unstemmed | Transcriptional Autoregulatory Loops Are Highly Conserved in Vertebrate Evolution |
title_short | Transcriptional Autoregulatory Loops Are Highly Conserved in Vertebrate Evolution |
title_sort | transcriptional autoregulatory loops are highly conserved in vertebrate evolution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527657/ https://www.ncbi.nlm.nih.gov/pubmed/18791639 http://dx.doi.org/10.1371/journal.pone.0003210 |
work_keys_str_mv | AT kiełbasaszymonm transcriptionalautoregulatoryloopsarehighlyconservedinvertebrateevolution AT vingronmartin transcriptionalautoregulatoryloopsarehighlyconservedinvertebrateevolution |