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Maternal control of visceral asymmetry evolution in Astyanax cavefish

The direction of visceral organ asymmetry is highly conserved during vertebrate evolution with heart development biased to the left and pancreas and liver development restricted to opposing sides of the midline. Here we show that reversals in visceral organ asymmetry have evolved in Astyanax mexican...

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Autores principales: Ma, Li, Ng, Mandy, Shi, Janet, Gore, Aniket V., Castranova, Daniel, Weinstein, Brant M., Jeffery, William R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119719/
https://www.ncbi.nlm.nih.gov/pubmed/33986376
http://dx.doi.org/10.1038/s41598-021-89702-6
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author Ma, Li
Ng, Mandy
Shi, Janet
Gore, Aniket V.
Castranova, Daniel
Weinstein, Brant M.
Jeffery, William R.
author_facet Ma, Li
Ng, Mandy
Shi, Janet
Gore, Aniket V.
Castranova, Daniel
Weinstein, Brant M.
Jeffery, William R.
author_sort Ma, Li
collection PubMed
description The direction of visceral organ asymmetry is highly conserved during vertebrate evolution with heart development biased to the left and pancreas and liver development restricted to opposing sides of the midline. Here we show that reversals in visceral organ asymmetry have evolved in Astyanax mexicanus, a teleost species with interfertile surface-dwelling (surface fish) and cave-dwelling (cavefish) forms. Visceral organ asymmetry is conventional in surface fish but some cavefish have evolved reversals in heart, liver, and pancreas development. Corresponding changes in the normally left-sided expression of the Nodal-Pitx2/Lefty signaling system are also present in the cavefish lateral plate mesoderm (LPM). The Nodal antagonists lefty1 (lft1) and lefty2 (lft2), which confine Nodal signaling to the left LPM, are expressed in most surface fish, however, lft2, but not lft1, expression is absent during somitogenesis of most cavefish. Despite this difference, multiple lines of evidence suggested that evolutionary changes in L-R patterning are controlled upstream of Nodal-Pitx2/Lefty signaling. Accordingly, reciprocal hybridization of cavefish and surface fish showed that modifications of heart asymmetry are present in hybrids derived from cavefish mothers but not from surface fish mothers. The results indicate that changes in visceral asymmetry during cavefish evolution are influenced by maternal genetic effects.
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spelling pubmed-81197192021-05-17 Maternal control of visceral asymmetry evolution in Astyanax cavefish Ma, Li Ng, Mandy Shi, Janet Gore, Aniket V. Castranova, Daniel Weinstein, Brant M. Jeffery, William R. Sci Rep Article The direction of visceral organ asymmetry is highly conserved during vertebrate evolution with heart development biased to the left and pancreas and liver development restricted to opposing sides of the midline. Here we show that reversals in visceral organ asymmetry have evolved in Astyanax mexicanus, a teleost species with interfertile surface-dwelling (surface fish) and cave-dwelling (cavefish) forms. Visceral organ asymmetry is conventional in surface fish but some cavefish have evolved reversals in heart, liver, and pancreas development. Corresponding changes in the normally left-sided expression of the Nodal-Pitx2/Lefty signaling system are also present in the cavefish lateral plate mesoderm (LPM). The Nodal antagonists lefty1 (lft1) and lefty2 (lft2), which confine Nodal signaling to the left LPM, are expressed in most surface fish, however, lft2, but not lft1, expression is absent during somitogenesis of most cavefish. Despite this difference, multiple lines of evidence suggested that evolutionary changes in L-R patterning are controlled upstream of Nodal-Pitx2/Lefty signaling. Accordingly, reciprocal hybridization of cavefish and surface fish showed that modifications of heart asymmetry are present in hybrids derived from cavefish mothers but not from surface fish mothers. The results indicate that changes in visceral asymmetry during cavefish evolution are influenced by maternal genetic effects. Nature Publishing Group UK 2021-05-13 /pmc/articles/PMC8119719/ /pubmed/33986376 http://dx.doi.org/10.1038/s41598-021-89702-6 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ma, Li
Ng, Mandy
Shi, Janet
Gore, Aniket V.
Castranova, Daniel
Weinstein, Brant M.
Jeffery, William R.
Maternal control of visceral asymmetry evolution in Astyanax cavefish
title Maternal control of visceral asymmetry evolution in Astyanax cavefish
title_full Maternal control of visceral asymmetry evolution in Astyanax cavefish
title_fullStr Maternal control of visceral asymmetry evolution in Astyanax cavefish
title_full_unstemmed Maternal control of visceral asymmetry evolution in Astyanax cavefish
title_short Maternal control of visceral asymmetry evolution in Astyanax cavefish
title_sort maternal control of visceral asymmetry evolution in astyanax cavefish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119719/
https://www.ncbi.nlm.nih.gov/pubmed/33986376
http://dx.doi.org/10.1038/s41598-021-89702-6
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