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Evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function
Animals are characterized by a set of highly conserved developmental regulators. Changes in the cis-regulatory elements of these regulators are thought to constitute the major driver of morphological evolution. However, the role of coding sequence evolution remains unresolved. To address this questi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432213/ https://www.ncbi.nlm.nih.gov/pubmed/28406397 http://dx.doi.org/10.7554/eLife.26402 |
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author | Weinberger, Simon Topping, Matthew P Yan, Jiekun Claeys, Annelies Geest, Natalie De Ozbay, Duru Hassan, Talah He, Xiaoli Albert, Joerg T Hassan, Bassem A Ramaekers, Ariane |
author_facet | Weinberger, Simon Topping, Matthew P Yan, Jiekun Claeys, Annelies Geest, Natalie De Ozbay, Duru Hassan, Talah He, Xiaoli Albert, Joerg T Hassan, Bassem A Ramaekers, Ariane |
author_sort | Weinberger, Simon |
collection | PubMed |
description | Animals are characterized by a set of highly conserved developmental regulators. Changes in the cis-regulatory elements of these regulators are thought to constitute the major driver of morphological evolution. However, the role of coding sequence evolution remains unresolved. To address this question, we used the Atonal family of proneural transcription factors as a model. Drosophila atonal coding sequence was endogenously replaced with that of atonal homologues (ATHs) at key phylogenetic positions, non-ATH proneural genes, and the closest homologue to ancestral proneural genes. ATHs and the ancestral-like coding sequences rescued sensory organ fate in atonal mutants, in contrast to non-ATHs. Surprisingly, different ATH factors displayed different levels of proneural activity as reflected by the number and functionality of sense organs. This proneural potency gradient correlated directly with ATH protein stability, including in response to Notch signaling, independently of mRNA levels or codon usage. This establishes a distinct and ancient function for ATHs and demonstrates that coding sequence evolution can underlie quantitative variation in sensory development and function. DOI: http://dx.doi.org/10.7554/eLife.26402.001 |
format | Online Article Text |
id | pubmed-5432213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54322132017-05-17 Evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function Weinberger, Simon Topping, Matthew P Yan, Jiekun Claeys, Annelies Geest, Natalie De Ozbay, Duru Hassan, Talah He, Xiaoli Albert, Joerg T Hassan, Bassem A Ramaekers, Ariane eLife Developmental Biology and Stem Cells Animals are characterized by a set of highly conserved developmental regulators. Changes in the cis-regulatory elements of these regulators are thought to constitute the major driver of morphological evolution. However, the role of coding sequence evolution remains unresolved. To address this question, we used the Atonal family of proneural transcription factors as a model. Drosophila atonal coding sequence was endogenously replaced with that of atonal homologues (ATHs) at key phylogenetic positions, non-ATH proneural genes, and the closest homologue to ancestral proneural genes. ATHs and the ancestral-like coding sequences rescued sensory organ fate in atonal mutants, in contrast to non-ATHs. Surprisingly, different ATH factors displayed different levels of proneural activity as reflected by the number and functionality of sense organs. This proneural potency gradient correlated directly with ATH protein stability, including in response to Notch signaling, independently of mRNA levels or codon usage. This establishes a distinct and ancient function for ATHs and demonstrates that coding sequence evolution can underlie quantitative variation in sensory development and function. DOI: http://dx.doi.org/10.7554/eLife.26402.001 eLife Sciences Publications, Ltd 2017-04-13 /pmc/articles/PMC5432213/ /pubmed/28406397 http://dx.doi.org/10.7554/eLife.26402 Text en © 2017, Weinberger et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Weinberger, Simon Topping, Matthew P Yan, Jiekun Claeys, Annelies Geest, Natalie De Ozbay, Duru Hassan, Talah He, Xiaoli Albert, Joerg T Hassan, Bassem A Ramaekers, Ariane Evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function |
title | Evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function |
title_full | Evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function |
title_fullStr | Evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function |
title_full_unstemmed | Evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function |
title_short | Evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function |
title_sort | evolutionary changes in transcription factor coding sequence quantitatively alter sensory organ development and function |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432213/ https://www.ncbi.nlm.nih.gov/pubmed/28406397 http://dx.doi.org/10.7554/eLife.26402 |
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