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Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish

The vertebrate inner ear is the sensory organ mediating hearing and balance. The entire organ develops from the otic placode, which itself originates from the otic-epibranchial progenitor domain (OEPD). Multiple studies in various species have shown the importance of the forkhead-box and distal-less...

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Autores principales: Ezhkova, Diana, Schwarzer, Simone, Spieß, Sandra, Geffarth, Michaela, Machate, Anja, Zöller, Daniela, Stucke, Johanna, Alexopoulou, Dimitra, Lesche, Mathias, Dahl, Andreas, Hans, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10261724/
https://www.ncbi.nlm.nih.gov/pubmed/37272628
http://dx.doi.org/10.1242/bio.059911
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author Ezhkova, Diana
Schwarzer, Simone
Spieß, Sandra
Geffarth, Michaela
Machate, Anja
Zöller, Daniela
Stucke, Johanna
Alexopoulou, Dimitra
Lesche, Mathias
Dahl, Andreas
Hans, Stefan
author_facet Ezhkova, Diana
Schwarzer, Simone
Spieß, Sandra
Geffarth, Michaela
Machate, Anja
Zöller, Daniela
Stucke, Johanna
Alexopoulou, Dimitra
Lesche, Mathias
Dahl, Andreas
Hans, Stefan
author_sort Ezhkova, Diana
collection PubMed
description The vertebrate inner ear is the sensory organ mediating hearing and balance. The entire organ develops from the otic placode, which itself originates from the otic-epibranchial progenitor domain (OEPD). Multiple studies in various species have shown the importance of the forkhead-box and distal-less homeodomain transcription factor families for OEPD and subsequent otic placode formation. However, the transcriptional networks downstream of these factors are only beginning to be understood. Using transcriptome analysis, we here reveal numerous genes regulated by the distal-less homeodomain transcription factors Dlx3b and Dlx4b (Dlx3b/4b). We identify known and novel transcripts displaying widespread OEPD expression in a Dlx3b/4b-dependent manner. Some genes, with a known OEPD expression in other vertebrate species, might be members of a presumptive vertebrate core module required for proper otic development. Moreover, we identify genes controlling early-born sensory hair cell formation as well as regulating biomineral tissue development, both consistent with defective sensory hair cell and otolith formation observed in dlx3b/4b mutants. Finally, we show that ectopic Atoh1b expression can rescue early sensorigenesis even in the absence of Dlx3b/4b. Taken together, our data will help to unravel the gene regulatory network underlying early inner ear development and provide insights into the molecular control of vertebrate inner ear formation to restore hearing loss in humans ultimately.
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spelling pubmed-102617242023-06-15 Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish Ezhkova, Diana Schwarzer, Simone Spieß, Sandra Geffarth, Michaela Machate, Anja Zöller, Daniela Stucke, Johanna Alexopoulou, Dimitra Lesche, Mathias Dahl, Andreas Hans, Stefan Biol Open Research Article The vertebrate inner ear is the sensory organ mediating hearing and balance. The entire organ develops from the otic placode, which itself originates from the otic-epibranchial progenitor domain (OEPD). Multiple studies in various species have shown the importance of the forkhead-box and distal-less homeodomain transcription factor families for OEPD and subsequent otic placode formation. However, the transcriptional networks downstream of these factors are only beginning to be understood. Using transcriptome analysis, we here reveal numerous genes regulated by the distal-less homeodomain transcription factors Dlx3b and Dlx4b (Dlx3b/4b). We identify known and novel transcripts displaying widespread OEPD expression in a Dlx3b/4b-dependent manner. Some genes, with a known OEPD expression in other vertebrate species, might be members of a presumptive vertebrate core module required for proper otic development. Moreover, we identify genes controlling early-born sensory hair cell formation as well as regulating biomineral tissue development, both consistent with defective sensory hair cell and otolith formation observed in dlx3b/4b mutants. Finally, we show that ectopic Atoh1b expression can rescue early sensorigenesis even in the absence of Dlx3b/4b. Taken together, our data will help to unravel the gene regulatory network underlying early inner ear development and provide insights into the molecular control of vertebrate inner ear formation to restore hearing loss in humans ultimately. The Company of Biologists Ltd 2023-06-05 /pmc/articles/PMC10261724/ /pubmed/37272628 http://dx.doi.org/10.1242/bio.059911 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Ezhkova, Diana
Schwarzer, Simone
Spieß, Sandra
Geffarth, Michaela
Machate, Anja
Zöller, Daniela
Stucke, Johanna
Alexopoulou, Dimitra
Lesche, Mathias
Dahl, Andreas
Hans, Stefan
Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish
title Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish
title_full Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish
title_fullStr Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish
title_full_unstemmed Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish
title_short Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish
title_sort transcriptome analysis reveals an atoh1b-dependent gene set downstream of dlx3b/4b during early inner ear development in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10261724/
https://www.ncbi.nlm.nih.gov/pubmed/37272628
http://dx.doi.org/10.1242/bio.059911
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