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Heterotachy in Mammalian Promoter Evolution
We have surveyed the evolutionary trends of mammalian promoters and upstream sequences, utilising large sets of experimentally supported transcription start sites (TSSs). With 30,969 well-defined TSSs from mouse and 26,341 from human, there are sufficient numbers to draw statistically meaningful con...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1449885/ https://www.ncbi.nlm.nih.gov/pubmed/16683025 http://dx.doi.org/10.1371/journal.pgen.0020030 |
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author | Taylor, Martin S Kai, Chikatoshi Kawai, Jun Carninci, Piero Hayashizaki, Yoshihide Semple, Colin A. M |
author_facet | Taylor, Martin S Kai, Chikatoshi Kawai, Jun Carninci, Piero Hayashizaki, Yoshihide Semple, Colin A. M |
author_sort | Taylor, Martin S |
collection | PubMed |
description | We have surveyed the evolutionary trends of mammalian promoters and upstream sequences, utilising large sets of experimentally supported transcription start sites (TSSs). With 30,969 well-defined TSSs from mouse and 26,341 from human, there are sufficient numbers to draw statistically meaningful conclusions and to consider differences between promoter types. Unlike previous smaller studies, we have considered the effects of insertions, deletions, and transposable elements as well as nucleotide substitutions. The rate of promoter evolution relative to that of control sequences has not been consistent between lineages nor within lineages over time. The most pronounced manifestation of this heterotachy is the increased rate of evolution in primate promoters. This increase is seen across different classes of mutation, including substitutions and micro-indel events. We investigated the relationship between promoter and coding sequence selective constraint and suggest that they are generally uncorrelated. This analysis also identified a small number of mouse promoters associated with the immune response that are under positive selection in rodents. We demonstrate significant differences in divergence between functional promoter categories and identify a category of promoters, not associated with conventional protein-coding genes, that has the highest rates of divergence across mammals. We find that evolutionary rates vary both on a fine scale within mammalian promoters and also between different functional classes of promoters. The discovery of heterotachy in promoter evolution, in particular the accelerated evolution of primate promoters, has important implications for our understanding of human evolution and for strategies to detect primate-specific regulatory elements. |
format | Text |
id | pubmed-1449885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-14498852006-05-08 Heterotachy in Mammalian Promoter Evolution Taylor, Martin S Kai, Chikatoshi Kawai, Jun Carninci, Piero Hayashizaki, Yoshihide Semple, Colin A. M PLoS Genet Research Article We have surveyed the evolutionary trends of mammalian promoters and upstream sequences, utilising large sets of experimentally supported transcription start sites (TSSs). With 30,969 well-defined TSSs from mouse and 26,341 from human, there are sufficient numbers to draw statistically meaningful conclusions and to consider differences between promoter types. Unlike previous smaller studies, we have considered the effects of insertions, deletions, and transposable elements as well as nucleotide substitutions. The rate of promoter evolution relative to that of control sequences has not been consistent between lineages nor within lineages over time. The most pronounced manifestation of this heterotachy is the increased rate of evolution in primate promoters. This increase is seen across different classes of mutation, including substitutions and micro-indel events. We investigated the relationship between promoter and coding sequence selective constraint and suggest that they are generally uncorrelated. This analysis also identified a small number of mouse promoters associated with the immune response that are under positive selection in rodents. We demonstrate significant differences in divergence between functional promoter categories and identify a category of promoters, not associated with conventional protein-coding genes, that has the highest rates of divergence across mammals. We find that evolutionary rates vary both on a fine scale within mammalian promoters and also between different functional classes of promoters. The discovery of heterotachy in promoter evolution, in particular the accelerated evolution of primate promoters, has important implications for our understanding of human evolution and for strategies to detect primate-specific regulatory elements. Public Library of Science 2006-04 2006-04-28 /pmc/articles/PMC1449885/ /pubmed/16683025 http://dx.doi.org/10.1371/journal.pgen.0020030 Text en © 2006 Taylor 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 Taylor, Martin S Kai, Chikatoshi Kawai, Jun Carninci, Piero Hayashizaki, Yoshihide Semple, Colin A. M Heterotachy in Mammalian Promoter Evolution |
title | Heterotachy in Mammalian Promoter Evolution |
title_full | Heterotachy in Mammalian Promoter Evolution |
title_fullStr | Heterotachy in Mammalian Promoter Evolution |
title_full_unstemmed | Heterotachy in Mammalian Promoter Evolution |
title_short | Heterotachy in Mammalian Promoter Evolution |
title_sort | heterotachy in mammalian promoter evolution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1449885/ https://www.ncbi.nlm.nih.gov/pubmed/16683025 http://dx.doi.org/10.1371/journal.pgen.0020030 |
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