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Brain Sensory Organs of the Ascidian Ciona robusta: Structure, Function and Developmental Mechanisms
During evolution, new characters are designed by modifying pre-existing structures already present in ancient organisms. In this perspective, the Central Nervous System (CNS) of ascidian larva offers a good opportunity to analyze a complex phenomenon with a simplified approach. As sister group of ve...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450388/ https://www.ncbi.nlm.nih.gov/pubmed/34552923 http://dx.doi.org/10.3389/fcell.2021.701779 |
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author | Olivo, Paola Palladino, Antonio Ristoratore, Filomena Spagnuolo, Antonietta |
author_facet | Olivo, Paola Palladino, Antonio Ristoratore, Filomena Spagnuolo, Antonietta |
author_sort | Olivo, Paola |
collection | PubMed |
description | During evolution, new characters are designed by modifying pre-existing structures already present in ancient organisms. In this perspective, the Central Nervous System (CNS) of ascidian larva offers a good opportunity to analyze a complex phenomenon with a simplified approach. As sister group of vertebrates, ascidian tadpole larva exhibits a dorsal CNS, made up of only about 330 cells distributed into the anterior sensory brain vesicle (BV), connected to the motor ganglion (MG) and a caudal nerve cord (CNC) in the tail. Low number of cells does not mean, however, low complexity. The larval brain contains 177 neurons, for which a documented synaptic connectome is now available, and two pigmented organs, the otolith and the ocellus, controlling larval swimming behavior. The otolith is involved in gravity perception and the ocellus in light perception. Here, we specifically review the studies focused on the development of the building blocks of ascidians pigmented sensory organs, namely pigment cells and photoreceptor cells. We focus on what it is known, up to now, on the molecular bases of specification and differentiation of both lineages, on the function of these organs after larval hatching during pre-settlement period, and on the most cutting-edge technologies, like single cell RNAseq and genome editing CRISPR/CAS9, that, adapted and applied to Ciona embryos, are increasingly enhancing the tractability of Ciona for developmental studies, including pigmented organs formation. |
format | Online Article Text |
id | pubmed-8450388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84503882021-09-21 Brain Sensory Organs of the Ascidian Ciona robusta: Structure, Function and Developmental Mechanisms Olivo, Paola Palladino, Antonio Ristoratore, Filomena Spagnuolo, Antonietta Front Cell Dev Biol Cell and Developmental Biology During evolution, new characters are designed by modifying pre-existing structures already present in ancient organisms. In this perspective, the Central Nervous System (CNS) of ascidian larva offers a good opportunity to analyze a complex phenomenon with a simplified approach. As sister group of vertebrates, ascidian tadpole larva exhibits a dorsal CNS, made up of only about 330 cells distributed into the anterior sensory brain vesicle (BV), connected to the motor ganglion (MG) and a caudal nerve cord (CNC) in the tail. Low number of cells does not mean, however, low complexity. The larval brain contains 177 neurons, for which a documented synaptic connectome is now available, and two pigmented organs, the otolith and the ocellus, controlling larval swimming behavior. The otolith is involved in gravity perception and the ocellus in light perception. Here, we specifically review the studies focused on the development of the building blocks of ascidians pigmented sensory organs, namely pigment cells and photoreceptor cells. We focus on what it is known, up to now, on the molecular bases of specification and differentiation of both lineages, on the function of these organs after larval hatching during pre-settlement period, and on the most cutting-edge technologies, like single cell RNAseq and genome editing CRISPR/CAS9, that, adapted and applied to Ciona embryos, are increasingly enhancing the tractability of Ciona for developmental studies, including pigmented organs formation. Frontiers Media S.A. 2021-09-06 /pmc/articles/PMC8450388/ /pubmed/34552923 http://dx.doi.org/10.3389/fcell.2021.701779 Text en Copyright © 2021 Olivo, Palladino, Ristoratore and Spagnuolo. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Olivo, Paola Palladino, Antonio Ristoratore, Filomena Spagnuolo, Antonietta Brain Sensory Organs of the Ascidian Ciona robusta: Structure, Function and Developmental Mechanisms |
title | Brain Sensory Organs of the Ascidian Ciona robusta: Structure, Function and Developmental Mechanisms |
title_full | Brain Sensory Organs of the Ascidian Ciona robusta: Structure, Function and Developmental Mechanisms |
title_fullStr | Brain Sensory Organs of the Ascidian Ciona robusta: Structure, Function and Developmental Mechanisms |
title_full_unstemmed | Brain Sensory Organs of the Ascidian Ciona robusta: Structure, Function and Developmental Mechanisms |
title_short | Brain Sensory Organs of the Ascidian Ciona robusta: Structure, Function and Developmental Mechanisms |
title_sort | brain sensory organs of the ascidian ciona robusta: structure, function and developmental mechanisms |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450388/ https://www.ncbi.nlm.nih.gov/pubmed/34552923 http://dx.doi.org/10.3389/fcell.2021.701779 |
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