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Cell Type-Specific Responses to Wingless, Hedgehog and Decapentaplegic Are Essential for Patterning Early Eye-Antenna Disc in Drosophila

The Drosophila eye-antenna imaginal disc (ead) is a flattened sac of two-layered epithelia, from which most head structures are derived. Secreted morphogens like Wingless (Wg), Hedgehog (Hh), and Decapentaplegic (Dpp) are important for early patterning of ead, but the underlying mechanisms are still...

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Autores principales: Won, Jong-Hoon, Tsogtbartarr, Orkhon, Son, Wonseok, Singh, Amit, Choi, Kwang-Wook, Cho, Kyung-Ok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388393/
https://www.ncbi.nlm.nih.gov/pubmed/25849899
http://dx.doi.org/10.1371/journal.pone.0121999
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author Won, Jong-Hoon
Tsogtbartarr, Orkhon
Son, Wonseok
Singh, Amit
Choi, Kwang-Wook
Cho, Kyung-Ok
author_facet Won, Jong-Hoon
Tsogtbartarr, Orkhon
Son, Wonseok
Singh, Amit
Choi, Kwang-Wook
Cho, Kyung-Ok
author_sort Won, Jong-Hoon
collection PubMed
description The Drosophila eye-antenna imaginal disc (ead) is a flattened sac of two-layered epithelia, from which most head structures are derived. Secreted morphogens like Wingless (Wg), Hedgehog (Hh), and Decapentaplegic (Dpp) are important for early patterning of ead, but the underlying mechanisms are still largely unknown. To understand how these morphogens function in the ead of early larval stages, we used wg-LacZ and dpp-Gal4 markers for the examination of wild-type and mutant eads. We found that the ead immediately after hatching was crescent-shaped with the Bolwig’s nerve at the ventral edge, suggesting that it consists of dorsal domain. In a subsequent step, transcriptional induction of dpp in the cells along the Bolwig’s nerve was followed by rapid growth of the ventral domain. Both Wg and Hh were required for the formation of the ventral domain. Wg was crucial for the growth of the entire ead, but Hh was essential for cell division only in the dorsal domain. In the ventral domain, Hh regulated dpp transcription. Based on these data, we propose that signaling among distinct groups of cells expressing Wg, Dpp, or Hh in the ead of the first-instar larvae are critical for coordinated growth and patterning of ead.
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spelling pubmed-43883932015-04-21 Cell Type-Specific Responses to Wingless, Hedgehog and Decapentaplegic Are Essential for Patterning Early Eye-Antenna Disc in Drosophila Won, Jong-Hoon Tsogtbartarr, Orkhon Son, Wonseok Singh, Amit Choi, Kwang-Wook Cho, Kyung-Ok PLoS One Research Article The Drosophila eye-antenna imaginal disc (ead) is a flattened sac of two-layered epithelia, from which most head structures are derived. Secreted morphogens like Wingless (Wg), Hedgehog (Hh), and Decapentaplegic (Dpp) are important for early patterning of ead, but the underlying mechanisms are still largely unknown. To understand how these morphogens function in the ead of early larval stages, we used wg-LacZ and dpp-Gal4 markers for the examination of wild-type and mutant eads. We found that the ead immediately after hatching was crescent-shaped with the Bolwig’s nerve at the ventral edge, suggesting that it consists of dorsal domain. In a subsequent step, transcriptional induction of dpp in the cells along the Bolwig’s nerve was followed by rapid growth of the ventral domain. Both Wg and Hh were required for the formation of the ventral domain. Wg was crucial for the growth of the entire ead, but Hh was essential for cell division only in the dorsal domain. In the ventral domain, Hh regulated dpp transcription. Based on these data, we propose that signaling among distinct groups of cells expressing Wg, Dpp, or Hh in the ead of the first-instar larvae are critical for coordinated growth and patterning of ead. Public Library of Science 2015-04-07 /pmc/articles/PMC4388393/ /pubmed/25849899 http://dx.doi.org/10.1371/journal.pone.0121999 Text en © 2015 Won et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Won, Jong-Hoon
Tsogtbartarr, Orkhon
Son, Wonseok
Singh, Amit
Choi, Kwang-Wook
Cho, Kyung-Ok
Cell Type-Specific Responses to Wingless, Hedgehog and Decapentaplegic Are Essential for Patterning Early Eye-Antenna Disc in Drosophila
title Cell Type-Specific Responses to Wingless, Hedgehog and Decapentaplegic Are Essential for Patterning Early Eye-Antenna Disc in Drosophila
title_full Cell Type-Specific Responses to Wingless, Hedgehog and Decapentaplegic Are Essential for Patterning Early Eye-Antenna Disc in Drosophila
title_fullStr Cell Type-Specific Responses to Wingless, Hedgehog and Decapentaplegic Are Essential for Patterning Early Eye-Antenna Disc in Drosophila
title_full_unstemmed Cell Type-Specific Responses to Wingless, Hedgehog and Decapentaplegic Are Essential for Patterning Early Eye-Antenna Disc in Drosophila
title_short Cell Type-Specific Responses to Wingless, Hedgehog and Decapentaplegic Are Essential for Patterning Early Eye-Antenna Disc in Drosophila
title_sort cell type-specific responses to wingless, hedgehog and decapentaplegic are essential for patterning early eye-antenna disc in drosophila
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388393/
https://www.ncbi.nlm.nih.gov/pubmed/25849899
http://dx.doi.org/10.1371/journal.pone.0121999
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