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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
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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
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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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