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An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks
Threespine stickleback fish offer a powerful system to dissect the genetic basis of morphological evolution in nature. Marine sticklebacks have repeatedly invaded and adapted to numerous freshwater environments throughout the Northern hemisphere. In response to new diets in freshwater habitats, chan...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019817/ https://www.ncbi.nlm.nih.gov/pubmed/29902209 http://dx.doi.org/10.1371/journal.pgen.1007449 |
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author | Cleves, Phillip A. Hart, James C. Agoglia, Rachel M. Jimenez, Monica T. Erickson, Priscilla A. Gai, Linda Miller, Craig T. |
author_facet | Cleves, Phillip A. Hart, James C. Agoglia, Rachel M. Jimenez, Monica T. Erickson, Priscilla A. Gai, Linda Miller, Craig T. |
author_sort | Cleves, Phillip A. |
collection | PubMed |
description | Threespine stickleback fish offer a powerful system to dissect the genetic basis of morphological evolution in nature. Marine sticklebacks have repeatedly invaded and adapted to numerous freshwater environments throughout the Northern hemisphere. In response to new diets in freshwater habitats, changes in craniofacial morphology, including heritable increases in tooth number, have evolved in derived freshwater populations. Using a combination of quantitative genetics and genome resequencing, here we fine-mapped a quantitative trait locus (QTL) regulating evolved tooth gain to a cluster of ten QTL-associated single nucleotide variants, all within intron four of Bone Morphogenetic Protein 6 (Bmp6). Transgenic reporter assays revealed this intronic region contains a tooth enhancer. We induced mutations in Bmp6, revealing required roles for survival, growth, and tooth patterning. Transcriptional profiling of Bmp6 mutant dental tissues identified significant downregulation of a set of genes whose orthologs were previously shown to be expressed in quiescent mouse hair stem cells. Collectively these data support a model where mutations within a Bmp6 intronic tooth enhancer contribute to evolved tooth gain, and suggest that ancient shared genetic circuitry regulates the regeneration of diverse vertebrate epithelial appendages including mammalian hair and fish teeth. |
format | Online Article Text |
id | pubmed-6019817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60198172018-07-06 An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks Cleves, Phillip A. Hart, James C. Agoglia, Rachel M. Jimenez, Monica T. Erickson, Priscilla A. Gai, Linda Miller, Craig T. PLoS Genet Research Article Threespine stickleback fish offer a powerful system to dissect the genetic basis of morphological evolution in nature. Marine sticklebacks have repeatedly invaded and adapted to numerous freshwater environments throughout the Northern hemisphere. In response to new diets in freshwater habitats, changes in craniofacial morphology, including heritable increases in tooth number, have evolved in derived freshwater populations. Using a combination of quantitative genetics and genome resequencing, here we fine-mapped a quantitative trait locus (QTL) regulating evolved tooth gain to a cluster of ten QTL-associated single nucleotide variants, all within intron four of Bone Morphogenetic Protein 6 (Bmp6). Transgenic reporter assays revealed this intronic region contains a tooth enhancer. We induced mutations in Bmp6, revealing required roles for survival, growth, and tooth patterning. Transcriptional profiling of Bmp6 mutant dental tissues identified significant downregulation of a set of genes whose orthologs were previously shown to be expressed in quiescent mouse hair stem cells. Collectively these data support a model where mutations within a Bmp6 intronic tooth enhancer contribute to evolved tooth gain, and suggest that ancient shared genetic circuitry regulates the regeneration of diverse vertebrate epithelial appendages including mammalian hair and fish teeth. Public Library of Science 2018-06-14 /pmc/articles/PMC6019817/ /pubmed/29902209 http://dx.doi.org/10.1371/journal.pgen.1007449 Text en © 2018 Cleves 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Cleves, Phillip A. Hart, James C. Agoglia, Rachel M. Jimenez, Monica T. Erickson, Priscilla A. Gai, Linda Miller, Craig T. An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks |
title | An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks |
title_full | An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks |
title_fullStr | An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks |
title_full_unstemmed | An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks |
title_short | An intronic enhancer of Bmp6 underlies evolved tooth gain in sticklebacks |
title_sort | intronic enhancer of bmp6 underlies evolved tooth gain in sticklebacks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019817/ https://www.ncbi.nlm.nih.gov/pubmed/29902209 http://dx.doi.org/10.1371/journal.pgen.1007449 |
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