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Divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish
South American and African weakly electric fish independently evolved electric organs from muscle. In both groups, a voltage-gated sodium channel gene independently lost expression from muscle and gained it in the electric organ, allowing the channel to become specialized for generating electric sig...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9159570/ https://www.ncbi.nlm.nih.gov/pubmed/35648851 http://dx.doi.org/10.1126/sciadv.abm2970 |
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author | LaPotin, Sarah Swartz, Mary E. Luecke, David M. Constantinou, Savvas J. Gallant, Jason R. Eberhart, Johann K. Zakon, Harold H. |
author_facet | LaPotin, Sarah Swartz, Mary E. Luecke, David M. Constantinou, Savvas J. Gallant, Jason R. Eberhart, Johann K. Zakon, Harold H. |
author_sort | LaPotin, Sarah |
collection | PubMed |
description | South American and African weakly electric fish independently evolved electric organs from muscle. In both groups, a voltage-gated sodium channel gene independently lost expression from muscle and gained it in the electric organ, allowing the channel to become specialized for generating electric signals. It is unknown how this voltage-gated sodium channel gene is targeted to muscle in any vertebrate. We describe an enhancer that selectively targets sodium channel expression to muscle. Next, we demonstrate how the loss of this enhancer, but not trans-activating factors, drove the loss of sodium channel gene expression from muscle in South American electric fish. While this enhancer is also altered in African electric fish, key transcription factor binding sites and enhancer activity are retained, suggesting that the convergent loss of sodium channel expression from muscle in these two electric fish lineages occurred via different processes. |
format | Online Article Text |
id | pubmed-9159570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91595702022-06-16 Divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish LaPotin, Sarah Swartz, Mary E. Luecke, David M. Constantinou, Savvas J. Gallant, Jason R. Eberhart, Johann K. Zakon, Harold H. Sci Adv Biomedicine and Life Sciences South American and African weakly electric fish independently evolved electric organs from muscle. In both groups, a voltage-gated sodium channel gene independently lost expression from muscle and gained it in the electric organ, allowing the channel to become specialized for generating electric signals. It is unknown how this voltage-gated sodium channel gene is targeted to muscle in any vertebrate. We describe an enhancer that selectively targets sodium channel expression to muscle. Next, we demonstrate how the loss of this enhancer, but not trans-activating factors, drove the loss of sodium channel gene expression from muscle in South American electric fish. While this enhancer is also altered in African electric fish, key transcription factor binding sites and enhancer activity are retained, suggesting that the convergent loss of sodium channel expression from muscle in these two electric fish lineages occurred via different processes. American Association for the Advancement of Science 2022-06-01 /pmc/articles/PMC9159570/ /pubmed/35648851 http://dx.doi.org/10.1126/sciadv.abm2970 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences LaPotin, Sarah Swartz, Mary E. Luecke, David M. Constantinou, Savvas J. Gallant, Jason R. Eberhart, Johann K. Zakon, Harold H. Divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish |
title | Divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish |
title_full | Divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish |
title_fullStr | Divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish |
title_full_unstemmed | Divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish |
title_short | Divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish |
title_sort | divergent cis-regulatory evolution underlies the convergent loss of sodium channel expression in electric fish |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9159570/ https://www.ncbi.nlm.nih.gov/pubmed/35648851 http://dx.doi.org/10.1126/sciadv.abm2970 |
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