Cargando…

Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina

The vertebrate eye is a vital sensory organ that has long fascinated scientists, but the details of how this organ evolved are still unclear. The vertebrate eye is distinct from the simple photoreceptive organs of other non-vertebrate chordates and there are no clear transitional forms of the eye in...

Descripción completa

Detalles Bibliográficos
Autores principales: Bradshaw, Sarah N., Allison, W. Ted
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826474/
https://www.ncbi.nlm.nih.gov/pubmed/35155434
http://dx.doi.org/10.3389/fcell.2022.822358
_version_ 1784647439817375744
author Bradshaw, Sarah N.
Allison, W. Ted
author_facet Bradshaw, Sarah N.
Allison, W. Ted
author_sort Bradshaw, Sarah N.
collection PubMed
description The vertebrate eye is a vital sensory organ that has long fascinated scientists, but the details of how this organ evolved are still unclear. The vertebrate eye is distinct from the simple photoreceptive organs of other non-vertebrate chordates and there are no clear transitional forms of the eye in the fossil record. To investigate the evolution of the eye we can examine the eyes of the most ancient extant vertebrates, the hagfish and lamprey. These jawless vertebrates are in an ideal phylogenetic position to study the origin of the vertebrate eye but data on eye/retina development in these organisms is limited. New genomic and gene expression data from hagfish and lamprey suggest they have many of the same genes for eye development and retinal neurogenesis as jawed vertebrates, but functional work to determine if these genes operate in retinogenesis similarly to other vertebrates is missing. In addition, hagfish express a marker of proliferative retinal cells (Pax6) near the margin of the retina, and adult retinal growth is apparent in some species. This finding of eye growth late into hagfish ontogeny is unexpected given the degenerate eye phenotype. Further studies dissecting retinal neurogenesis in jawless vertebrates would allow for comparison of the mechanisms of retinal development between cyclostome and gnathostome eyes and provide insight into the evolutionary origins of the vertebrate eye.
format Online
Article
Text
id pubmed-8826474
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88264742022-02-10 Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina Bradshaw, Sarah N. Allison, W. Ted Front Cell Dev Biol Cell and Developmental Biology The vertebrate eye is a vital sensory organ that has long fascinated scientists, but the details of how this organ evolved are still unclear. The vertebrate eye is distinct from the simple photoreceptive organs of other non-vertebrate chordates and there are no clear transitional forms of the eye in the fossil record. To investigate the evolution of the eye we can examine the eyes of the most ancient extant vertebrates, the hagfish and lamprey. These jawless vertebrates are in an ideal phylogenetic position to study the origin of the vertebrate eye but data on eye/retina development in these organisms is limited. New genomic and gene expression data from hagfish and lamprey suggest they have many of the same genes for eye development and retinal neurogenesis as jawed vertebrates, but functional work to determine if these genes operate in retinogenesis similarly to other vertebrates is missing. In addition, hagfish express a marker of proliferative retinal cells (Pax6) near the margin of the retina, and adult retinal growth is apparent in some species. This finding of eye growth late into hagfish ontogeny is unexpected given the degenerate eye phenotype. Further studies dissecting retinal neurogenesis in jawless vertebrates would allow for comparison of the mechanisms of retinal development between cyclostome and gnathostome eyes and provide insight into the evolutionary origins of the vertebrate eye. Frontiers Media S.A. 2022-01-26 /pmc/articles/PMC8826474/ /pubmed/35155434 http://dx.doi.org/10.3389/fcell.2022.822358 Text en Copyright © 2022 Bradshaw and Allison. 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
Bradshaw, Sarah N.
Allison, W. Ted
Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina
title Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina
title_full Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina
title_fullStr Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina
title_full_unstemmed Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina
title_short Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina
title_sort hagfish to illuminate the developmental and evolutionary origins of the vertebrate retina
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826474/
https://www.ncbi.nlm.nih.gov/pubmed/35155434
http://dx.doi.org/10.3389/fcell.2022.822358
work_keys_str_mv AT bradshawsarahn hagfishtoilluminatethedevelopmentalandevolutionaryoriginsofthevertebrateretina
AT allisonwted hagfishtoilluminatethedevelopmentalandevolutionaryoriginsofthevertebrateretina