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Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges
BACKGROUND: The microvillus is a versatile organelle that serves important functions in disparate animal cell types. However, from a molecular perspective, the microvillus has been well studied in only a few, predominantly vertebrate, contexts. Little is known about how differences in microvillar st...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942974/ https://www.ncbi.nlm.nih.gov/pubmed/27413529 http://dx.doi.org/10.1186/s13227-016-0050-x |
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author | Peña, Jesús F. Alié, Alexandre Richter, Daniel J. Wang, Lingyu Funayama, Noriko Nichols, Scott A. |
author_facet | Peña, Jesús F. Alié, Alexandre Richter, Daniel J. Wang, Lingyu Funayama, Noriko Nichols, Scott A. |
author_sort | Peña, Jesús F. |
collection | PubMed |
description | BACKGROUND: The microvillus is a versatile organelle that serves important functions in disparate animal cell types. However, from a molecular perspective, the microvillus has been well studied in only a few, predominantly vertebrate, contexts. Little is known about how differences in microvillar structure contribute to differences in function, and how these differences evolved. We sequenced the transcriptome of the freshwater sponge, Ephydatia muelleri, and examined the expression of vertebrate microvillar gene homologs in choanocytes—the only microvilli-bearing cell type present in sponges. Sponges offer a distant phylogenetic comparison with vertebrates, and choanocytes are central to discussions about early animal evolution due to their similarity with choanoflagellates, the single-celled sister lineage of modern animals. RESULTS: We found that, from a genomic perspective, sponges have conserved homologs of most vertebrate microvillar genes, most of which are expressed in choanocytes, and many of which exhibit choanocyte-specific or choanocyte-enriched expression. Possible exceptions include the cadherins that form intermicrovillar links in the enterocyte brush border and hair cell stereocilia of vertebrates and cnidarians. No obvious orthologs of these proteins were detected in sponges, but at least four candidate cadherins were identified as choanocyte-enriched and might serve this function. In contrast to the evidence for conserved microvillar structure in sponges and vertebrates, we found that choanoflagellates and ctenophores lack homologs of many fundamental microvillar genes, suggesting that microvillar structure may diverge significantly in these lineages, warranting further study. CONCLUSIONS: The available evidence suggests that microvilli evolved early in the prehistory of modern animals and have been repurposed to serve myriad functions in different cellular contexts. Detailed understanding of the sequence by which different microvilli-bearing cell/tissue types diversified will require further study of microvillar composition and development in disparate cell types and lineages. Of particular interest are the microvilli of choanoflagellates, ctenophores, and sponges, which collectively bracket the earliest events in animal evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13227-016-0050-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4942974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49429742016-07-14 Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges Peña, Jesús F. Alié, Alexandre Richter, Daniel J. Wang, Lingyu Funayama, Noriko Nichols, Scott A. EvoDevo Research BACKGROUND: The microvillus is a versatile organelle that serves important functions in disparate animal cell types. However, from a molecular perspective, the microvillus has been well studied in only a few, predominantly vertebrate, contexts. Little is known about how differences in microvillar structure contribute to differences in function, and how these differences evolved. We sequenced the transcriptome of the freshwater sponge, Ephydatia muelleri, and examined the expression of vertebrate microvillar gene homologs in choanocytes—the only microvilli-bearing cell type present in sponges. Sponges offer a distant phylogenetic comparison with vertebrates, and choanocytes are central to discussions about early animal evolution due to their similarity with choanoflagellates, the single-celled sister lineage of modern animals. RESULTS: We found that, from a genomic perspective, sponges have conserved homologs of most vertebrate microvillar genes, most of which are expressed in choanocytes, and many of which exhibit choanocyte-specific or choanocyte-enriched expression. Possible exceptions include the cadherins that form intermicrovillar links in the enterocyte brush border and hair cell stereocilia of vertebrates and cnidarians. No obvious orthologs of these proteins were detected in sponges, but at least four candidate cadherins were identified as choanocyte-enriched and might serve this function. In contrast to the evidence for conserved microvillar structure in sponges and vertebrates, we found that choanoflagellates and ctenophores lack homologs of many fundamental microvillar genes, suggesting that microvillar structure may diverge significantly in these lineages, warranting further study. CONCLUSIONS: The available evidence suggests that microvilli evolved early in the prehistory of modern animals and have been repurposed to serve myriad functions in different cellular contexts. Detailed understanding of the sequence by which different microvilli-bearing cell/tissue types diversified will require further study of microvillar composition and development in disparate cell types and lineages. Of particular interest are the microvilli of choanoflagellates, ctenophores, and sponges, which collectively bracket the earliest events in animal evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13227-016-0050-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-12 /pmc/articles/PMC4942974/ /pubmed/27413529 http://dx.doi.org/10.1186/s13227-016-0050-x Text en © The Author(s) 2016 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 Peña, Jesús F. Alié, Alexandre Richter, Daniel J. Wang, Lingyu Funayama, Noriko Nichols, Scott A. Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges |
title | Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges |
title_full | Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges |
title_fullStr | Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges |
title_full_unstemmed | Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges |
title_short | Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges |
title_sort | conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942974/ https://www.ncbi.nlm.nih.gov/pubmed/27413529 http://dx.doi.org/10.1186/s13227-016-0050-x |
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