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The role of a lens survival pathway including sox2 and αA-crystallin in the evolution of cavefish eye degeneration

BACKGROUND: The teleost Astyanax mexicanus is a single species consisting of eyed surface-dwelling (surface fish) and blind cave-dwelling (cavefish) morphs. Cavefish eyes are lost through apoptosis of the lens, which in turn promotes the degeneration of other optic tissues. The αA-crystallin (αA-cry...

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Autores principales: Ma, Li, Parkhurst, Amy, Jeffery, William R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160140/
https://www.ncbi.nlm.nih.gov/pubmed/25210614
http://dx.doi.org/10.1186/2041-9139-5-28
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author Ma, Li
Parkhurst, Amy
Jeffery, William R
author_facet Ma, Li
Parkhurst, Amy
Jeffery, William R
author_sort Ma, Li
collection PubMed
description BACKGROUND: The teleost Astyanax mexicanus is a single species consisting of eyed surface-dwelling (surface fish) and blind cave-dwelling (cavefish) morphs. Cavefish eyes are lost through apoptosis of the lens, which in turn promotes the degeneration of other optic tissues. The αA-crystallin (αA-crys) gene is strongly downregulated in the cavefish lens and is located in a genomic region (QTL) responsible for eye loss. Therefore, αA-crys has been proposed as a candidate for regulating cavefish eye degeneration. The purpose of this study was to determine the mechanism of αA-crys downregulation and its role in cavefish eye degeneration. RESULTS: The involvement of αA-crys in eye degeneration was confirmed by knocking down its expression in surface fish, which led to apoptosis of the lens. The underlying reason for αA-crys downregulation in cavefish was investigated by comparing genomic αA-crys DNA sequences in surface fish and cavefish, however, no obvious cis-regulatory factors were discovered. Furthermore, the cavefish αA-crys allele is expressed in surface fish x cavefish F1 hybrids, indicating that evolutionary changes in upstream genes are most likely responsible for αA-crys downregulation. In other species, Sox2 is one of the transcription factors that regulate lens crystallin genes during eye development. Determination of sox2 expression patterns during surface fish and cavefish development showed that sox2 is specifically downregulated in the cavefish lens. The upstream regulatory function of Sox2 was demonstrated by knockdown in surface fish, which abolished αA-crys expression and induced lens apoptosis. CONCLUSIONS: The results suggest that αA-crys is required for normal eye development in cavefish via suppression of lens apoptosis. The regulatory changes involved in αA-crys downregulation in cavefish are in trans-acting factors rather than cis-acting mutations in the αA-crys gene. Therefore, αA-crys is unlikely to be the mutated gene(s) associated with an Astyanax eye QTL. The results reveal a genetic pathway leading from sox2 to αA-crys that is required for survival of the lens in Astyanax surface fish. Defects in this pathway may be involved in lens apoptosis and thus a cause of cavefish eye degeneration.
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spelling pubmed-41601402014-09-11 The role of a lens survival pathway including sox2 and αA-crystallin in the evolution of cavefish eye degeneration Ma, Li Parkhurst, Amy Jeffery, William R EvoDevo Research BACKGROUND: The teleost Astyanax mexicanus is a single species consisting of eyed surface-dwelling (surface fish) and blind cave-dwelling (cavefish) morphs. Cavefish eyes are lost through apoptosis of the lens, which in turn promotes the degeneration of other optic tissues. The αA-crystallin (αA-crys) gene is strongly downregulated in the cavefish lens and is located in a genomic region (QTL) responsible for eye loss. Therefore, αA-crys has been proposed as a candidate for regulating cavefish eye degeneration. The purpose of this study was to determine the mechanism of αA-crys downregulation and its role in cavefish eye degeneration. RESULTS: The involvement of αA-crys in eye degeneration was confirmed by knocking down its expression in surface fish, which led to apoptosis of the lens. The underlying reason for αA-crys downregulation in cavefish was investigated by comparing genomic αA-crys DNA sequences in surface fish and cavefish, however, no obvious cis-regulatory factors were discovered. Furthermore, the cavefish αA-crys allele is expressed in surface fish x cavefish F1 hybrids, indicating that evolutionary changes in upstream genes are most likely responsible for αA-crys downregulation. In other species, Sox2 is one of the transcription factors that regulate lens crystallin genes during eye development. Determination of sox2 expression patterns during surface fish and cavefish development showed that sox2 is specifically downregulated in the cavefish lens. The upstream regulatory function of Sox2 was demonstrated by knockdown in surface fish, which abolished αA-crys expression and induced lens apoptosis. CONCLUSIONS: The results suggest that αA-crys is required for normal eye development in cavefish via suppression of lens apoptosis. The regulatory changes involved in αA-crys downregulation in cavefish are in trans-acting factors rather than cis-acting mutations in the αA-crys gene. Therefore, αA-crys is unlikely to be the mutated gene(s) associated with an Astyanax eye QTL. The results reveal a genetic pathway leading from sox2 to αA-crys that is required for survival of the lens in Astyanax surface fish. Defects in this pathway may be involved in lens apoptosis and thus a cause of cavefish eye degeneration. BioMed Central 2014-08-28 /pmc/articles/PMC4160140/ /pubmed/25210614 http://dx.doi.org/10.1186/2041-9139-5-28 Text en Copyright © 2014 Ma et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Ma, Li
Parkhurst, Amy
Jeffery, William R
The role of a lens survival pathway including sox2 and αA-crystallin in the evolution of cavefish eye degeneration
title The role of a lens survival pathway including sox2 and αA-crystallin in the evolution of cavefish eye degeneration
title_full The role of a lens survival pathway including sox2 and αA-crystallin in the evolution of cavefish eye degeneration
title_fullStr The role of a lens survival pathway including sox2 and αA-crystallin in the evolution of cavefish eye degeneration
title_full_unstemmed The role of a lens survival pathway including sox2 and αA-crystallin in the evolution of cavefish eye degeneration
title_short The role of a lens survival pathway including sox2 and αA-crystallin in the evolution of cavefish eye degeneration
title_sort role of a lens survival pathway including sox2 and αa-crystallin in the evolution of cavefish eye degeneration
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160140/
https://www.ncbi.nlm.nih.gov/pubmed/25210614
http://dx.doi.org/10.1186/2041-9139-5-28
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