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Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor
Mammals have evolved remarkably different sensory, reproductive, metabolic, and skeletal systems. To explore the genetic basis for these differences, we developed a comparative genomics approach to scan whole-genome multiple sequence alignments to identify regions that evolved rapidly in an ancestra...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776709/ https://www.ncbi.nlm.nih.gov/pubmed/26715627 http://dx.doi.org/10.1093/molbev/msv344 |
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author | Holloway, Alisha K. Bruneau, Benoit G. Sukonnik, Tatyana Rubenstein, John L. Pollard, Katherine S. |
author_facet | Holloway, Alisha K. Bruneau, Benoit G. Sukonnik, Tatyana Rubenstein, John L. Pollard, Katherine S. |
author_sort | Holloway, Alisha K. |
collection | PubMed |
description | Mammals have evolved remarkably different sensory, reproductive, metabolic, and skeletal systems. To explore the genetic basis for these differences, we developed a comparative genomics approach to scan whole-genome multiple sequence alignments to identify regions that evolved rapidly in an ancestral lineage but are conserved within extant species. This pattern suggests that ancestral changes in function were maintained in descendants. After applying this test to therian mammals, we identified 4,797 accelerated regions, many of which are noncoding and located near developmental transcription factors. We then used mouse transgenic reporter assays to test if noncoding accelerated regions are enhancers and to determine how therian-specific substitutions affect their activity in vivo. We discovered enhancers with expression specific to the therian version in brain regions involved in the hormonal control of milk ejection, uterine contractions, blood pressure, temperature, and visual processing. This work underscores the idea that changes in developmental gene expression are important for mammalian evolution, and it pinpoints candidate genes for unique aspects of mammalian biology. |
format | Online Article Text |
id | pubmed-4776709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47767092016-03-04 Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor Holloway, Alisha K. Bruneau, Benoit G. Sukonnik, Tatyana Rubenstein, John L. Pollard, Katherine S. Mol Biol Evol Discoveries Mammals have evolved remarkably different sensory, reproductive, metabolic, and skeletal systems. To explore the genetic basis for these differences, we developed a comparative genomics approach to scan whole-genome multiple sequence alignments to identify regions that evolved rapidly in an ancestral lineage but are conserved within extant species. This pattern suggests that ancestral changes in function were maintained in descendants. After applying this test to therian mammals, we identified 4,797 accelerated regions, many of which are noncoding and located near developmental transcription factors. We then used mouse transgenic reporter assays to test if noncoding accelerated regions are enhancers and to determine how therian-specific substitutions affect their activity in vivo. We discovered enhancers with expression specific to the therian version in brain regions involved in the hormonal control of milk ejection, uterine contractions, blood pressure, temperature, and visual processing. This work underscores the idea that changes in developmental gene expression are important for mammalian evolution, and it pinpoints candidate genes for unique aspects of mammalian biology. Oxford University Press 2016-04 2015-12-29 /pmc/articles/PMC4776709/ /pubmed/26715627 http://dx.doi.org/10.1093/molbev/msv344 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Holloway, Alisha K. Bruneau, Benoit G. Sukonnik, Tatyana Rubenstein, John L. Pollard, Katherine S. Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor |
title | Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor |
title_full | Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor |
title_fullStr | Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor |
title_full_unstemmed | Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor |
title_short | Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor |
title_sort | accelerated evolution of enhancer hotspots in the mammal ancestor |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776709/ https://www.ncbi.nlm.nih.gov/pubmed/26715627 http://dx.doi.org/10.1093/molbev/msv344 |
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