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Molecular, phylogenetic and developmental analyses of Sall proteins in bilaterians
BACKGROUND: Sall (Spalt-like) proteins are zinc-finger transcription factors involved in a number of biological processes. They have only been studied in a few model organisms, such as Drosophila melanogaster, Caenorhabditis elegans, Schmidtea mediterranea and some vertebrates. Further taxon samplin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892016/ https://www.ncbi.nlm.nih.gov/pubmed/29644029 http://dx.doi.org/10.1186/s13227-018-0096-z |
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author | Lorente-Sorolla, José Truchado-Garcia, Marta Perry, Kimberly J. Henry, Jonathan Q. Grande, Cristina |
author_facet | Lorente-Sorolla, José Truchado-Garcia, Marta Perry, Kimberly J. Henry, Jonathan Q. Grande, Cristina |
author_sort | Lorente-Sorolla, José |
collection | PubMed |
description | BACKGROUND: Sall (Spalt-like) proteins are zinc-finger transcription factors involved in a number of biological processes. They have only been studied in a few model organisms, such as Drosophila melanogaster, Caenorhabditis elegans, Schmidtea mediterranea and some vertebrates. Further taxon sampling is critical to understand the evolution and diversification of this protein and its functional roles in animals. RESULTS: Using genome and transcriptome mining, we confirmed the presence of sall genes in a range of additional animal taxa, for which their presence had not yet been described. We show that sall genes are broadly conserved across the Bilateria, and likely appeared in the bilaterian stem lineage. Our analysis of the protein domains shows that the characteristic arrangement of the multiple zinc-finger domains is conserved in bilaterians and may represent the ancient arrangement of this family of transcription factors. We also show the existence of a previously unknown zinc-finger domain. In situ hybridization was used to describe the gene expression patterns in embryonic and larval stages in two species of snails: Crepidula fornicata and Lottia gigantea. In L. gigantea, sall presents maternal expression, although later on the expression is restricted to the A and B quadrants during gastrulation and larval stage. In C. fornicata, sall has no maternal expression and it is expressed mainly in the A, C and D quadrants during blastula stages and in an asymmetric fashion during the larval stage. DISCUSSION: Our results suggest that the bilaterian common ancestor had a Sall protein with at least six zinc-finger domains. The evolution of Sall proteins in bilaterians might have occurred mostly as a result of the loss of protein domains and gene duplications leading to diversification. The new evidence complements previous studies in highlighting an important role of Sall proteins in bilaterian development. Our results show maternal expression of sall in the snail L. gigantea, but not C. fornicata. The asymmetric expression shown in the ectoderm of the trochophore larva of snails is probably related to shell/mantle development. The observed sall expression in cephalic tissue in snails and some other bilaterians suggests a possible ancestral role of sall in neural development in bilaterians. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13227-018-0096-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5892016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58920162018-04-11 Molecular, phylogenetic and developmental analyses of Sall proteins in bilaterians Lorente-Sorolla, José Truchado-Garcia, Marta Perry, Kimberly J. Henry, Jonathan Q. Grande, Cristina EvoDevo Research BACKGROUND: Sall (Spalt-like) proteins are zinc-finger transcription factors involved in a number of biological processes. They have only been studied in a few model organisms, such as Drosophila melanogaster, Caenorhabditis elegans, Schmidtea mediterranea and some vertebrates. Further taxon sampling is critical to understand the evolution and diversification of this protein and its functional roles in animals. RESULTS: Using genome and transcriptome mining, we confirmed the presence of sall genes in a range of additional animal taxa, for which their presence had not yet been described. We show that sall genes are broadly conserved across the Bilateria, and likely appeared in the bilaterian stem lineage. Our analysis of the protein domains shows that the characteristic arrangement of the multiple zinc-finger domains is conserved in bilaterians and may represent the ancient arrangement of this family of transcription factors. We also show the existence of a previously unknown zinc-finger domain. In situ hybridization was used to describe the gene expression patterns in embryonic and larval stages in two species of snails: Crepidula fornicata and Lottia gigantea. In L. gigantea, sall presents maternal expression, although later on the expression is restricted to the A and B quadrants during gastrulation and larval stage. In C. fornicata, sall has no maternal expression and it is expressed mainly in the A, C and D quadrants during blastula stages and in an asymmetric fashion during the larval stage. DISCUSSION: Our results suggest that the bilaterian common ancestor had a Sall protein with at least six zinc-finger domains. The evolution of Sall proteins in bilaterians might have occurred mostly as a result of the loss of protein domains and gene duplications leading to diversification. The new evidence complements previous studies in highlighting an important role of Sall proteins in bilaterian development. Our results show maternal expression of sall in the snail L. gigantea, but not C. fornicata. The asymmetric expression shown in the ectoderm of the trochophore larva of snails is probably related to shell/mantle development. The observed sall expression in cephalic tissue in snails and some other bilaterians suggests a possible ancestral role of sall in neural development in bilaterians. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13227-018-0096-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-10 /pmc/articles/PMC5892016/ /pubmed/29644029 http://dx.doi.org/10.1186/s13227-018-0096-z Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lorente-Sorolla, José Truchado-Garcia, Marta Perry, Kimberly J. Henry, Jonathan Q. Grande, Cristina Molecular, phylogenetic and developmental analyses of Sall proteins in bilaterians |
title | Molecular, phylogenetic and developmental analyses of Sall proteins in bilaterians |
title_full | Molecular, phylogenetic and developmental analyses of Sall proteins in bilaterians |
title_fullStr | Molecular, phylogenetic and developmental analyses of Sall proteins in bilaterians |
title_full_unstemmed | Molecular, phylogenetic and developmental analyses of Sall proteins in bilaterians |
title_short | Molecular, phylogenetic and developmental analyses of Sall proteins in bilaterians |
title_sort | molecular, phylogenetic and developmental analyses of sall proteins in bilaterians |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892016/ https://www.ncbi.nlm.nih.gov/pubmed/29644029 http://dx.doi.org/10.1186/s13227-018-0096-z |
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