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Mutational scans reveal differential evolvability of Drosophila promoters and enhancers

Rapid enhancer and slow promoter evolution have been demonstrated through comparative genomics. However, it is not clear how this information is encoded genetically and if this can be used to place evolution in a predictive context. Part of the challenge is that our understanding of the potential fo...

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Autores principales: Li, Xueying C., Fuqua, Timothy, van Breugel, Maria Elize, Crocker, Justin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067265/
https://www.ncbi.nlm.nih.gov/pubmed/37004721
http://dx.doi.org/10.1098/rstb.2022.0054
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author Li, Xueying C.
Fuqua, Timothy
van Breugel, Maria Elize
Crocker, Justin
author_facet Li, Xueying C.
Fuqua, Timothy
van Breugel, Maria Elize
Crocker, Justin
author_sort Li, Xueying C.
collection PubMed
description Rapid enhancer and slow promoter evolution have been demonstrated through comparative genomics. However, it is not clear how this information is encoded genetically and if this can be used to place evolution in a predictive context. Part of the challenge is that our understanding of the potential for regulatory evolution is biased primarily toward natural variation or limited experimental perturbations. Here, to explore the evolutionary capacity of promoter variation, we surveyed an unbiased mutation library for three promoters in Drosophila melanogaster. We found that mutations in promoters had limited to no effect on spatial patterns of gene expression. Compared to developmental enhancers, promoters are more robust to mutations and have more access to mutations that can increase gene expression, suggesting that their low activity might be a result of selection. Consistent with these observations, increasing the promoter activity at the endogenous locus of shavenbaby led to increased transcription yet limited phenotypic changes. Taken together, developmental promoters may encode robust transcriptional outputs allowing evolvability through the integration of diverse developmental enhancers. This article is part of the theme issue ‘Interdisciplinary approaches to predicting evolutionary biology’.
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spelling pubmed-100672652023-04-03 Mutational scans reveal differential evolvability of Drosophila promoters and enhancers Li, Xueying C. Fuqua, Timothy van Breugel, Maria Elize Crocker, Justin Philos Trans R Soc Lond B Biol Sci Articles Rapid enhancer and slow promoter evolution have been demonstrated through comparative genomics. However, it is not clear how this information is encoded genetically and if this can be used to place evolution in a predictive context. Part of the challenge is that our understanding of the potential for regulatory evolution is biased primarily toward natural variation or limited experimental perturbations. Here, to explore the evolutionary capacity of promoter variation, we surveyed an unbiased mutation library for three promoters in Drosophila melanogaster. We found that mutations in promoters had limited to no effect on spatial patterns of gene expression. Compared to developmental enhancers, promoters are more robust to mutations and have more access to mutations that can increase gene expression, suggesting that their low activity might be a result of selection. Consistent with these observations, increasing the promoter activity at the endogenous locus of shavenbaby led to increased transcription yet limited phenotypic changes. Taken together, developmental promoters may encode robust transcriptional outputs allowing evolvability through the integration of diverse developmental enhancers. This article is part of the theme issue ‘Interdisciplinary approaches to predicting evolutionary biology’. The Royal Society 2023-05-22 2023-04-03 /pmc/articles/PMC10067265/ /pubmed/37004721 http://dx.doi.org/10.1098/rstb.2022.0054 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Li, Xueying C.
Fuqua, Timothy
van Breugel, Maria Elize
Crocker, Justin
Mutational scans reveal differential evolvability of Drosophila promoters and enhancers
title Mutational scans reveal differential evolvability of Drosophila promoters and enhancers
title_full Mutational scans reveal differential evolvability of Drosophila promoters and enhancers
title_fullStr Mutational scans reveal differential evolvability of Drosophila promoters and enhancers
title_full_unstemmed Mutational scans reveal differential evolvability of Drosophila promoters and enhancers
title_short Mutational scans reveal differential evolvability of Drosophila promoters and enhancers
title_sort mutational scans reveal differential evolvability of drosophila promoters and enhancers
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067265/
https://www.ncbi.nlm.nih.gov/pubmed/37004721
http://dx.doi.org/10.1098/rstb.2022.0054
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