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Common Transcriptional Mechanisms for Visual Photoreceptor Cell Differentiation among Pancrustaceans

A hallmark of visual rhabdomeric photoreceptors is the expression of a rhabdomeric opsin and uniquely associated phototransduction molecules, which are incorporated into a specialized expanded apical membrane, the rhabdomere. Given the extensive utilization of rhabdomeric photoreceptors in the eyes...

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Autores principales: Mahato, Simpla, Morita, Shinichi, Tucker, Abraham E., Liang, Xulong, Jackowska, Magdalena, Friedrich, Markus, Shiga, Yasuhiro, Zelhof, Andrew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084641/
https://www.ncbi.nlm.nih.gov/pubmed/24991928
http://dx.doi.org/10.1371/journal.pgen.1004484
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author Mahato, Simpla
Morita, Shinichi
Tucker, Abraham E.
Liang, Xulong
Jackowska, Magdalena
Friedrich, Markus
Shiga, Yasuhiro
Zelhof, Andrew C.
author_facet Mahato, Simpla
Morita, Shinichi
Tucker, Abraham E.
Liang, Xulong
Jackowska, Magdalena
Friedrich, Markus
Shiga, Yasuhiro
Zelhof, Andrew C.
author_sort Mahato, Simpla
collection PubMed
description A hallmark of visual rhabdomeric photoreceptors is the expression of a rhabdomeric opsin and uniquely associated phototransduction molecules, which are incorporated into a specialized expanded apical membrane, the rhabdomere. Given the extensive utilization of rhabdomeric photoreceptors in the eyes of protostomes, here we address whether a common transcriptional mechanism exists for the differentiation of rhabdomeric photoreceptors. In Drosophila, the transcription factors Pph13 and Orthodenticle (Otd) direct both aspects of differentiation: rhabdomeric opsin transcription and rhabdomere morphogenesis. We demonstrate that the orthologs of both proteins are expressed in the visual systems of the distantly related arthropod species Tribolium castaneum and Daphnia magna and that their functional roles are similar in these species. In particular, we establish that the Pph13 homologs have the ability to bind a subset of Rhodopsin core sequence I sites and that these sites are present in key phototransduction genes of both Tribolium and Daphnia. Furthermore, Pph13 and Otd orthologs are capable of executing deeply conserved functions of photoreceptor differentiation as evidenced by the ability to rescue their respective Drosophila mutant phenotypes. Pph13 homologs are equivalent in their ability to direct both rhabdomere morphogenesis and opsin expression within Drosophila, whereas Otd paralogs demonstrate differential abilities to regulate photoreceptor differentiation. Finally, loss-of-function analyses in Tribolium confirm the conserved requirement of Pph13 and Otd in regulating both rhabdomeric opsin transcription and rhabdomere morphogenesis. Taken together, our data identify components of a regulatory framework for rhabdomeric photoreceptor differentiation in Pancrustaceans, providing a foundation for defining ancestral regulatory modules of rhabdomeric photoreceptor differentiation.
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spelling pubmed-40846412014-07-10 Common Transcriptional Mechanisms for Visual Photoreceptor Cell Differentiation among Pancrustaceans Mahato, Simpla Morita, Shinichi Tucker, Abraham E. Liang, Xulong Jackowska, Magdalena Friedrich, Markus Shiga, Yasuhiro Zelhof, Andrew C. PLoS Genet Research Article A hallmark of visual rhabdomeric photoreceptors is the expression of a rhabdomeric opsin and uniquely associated phototransduction molecules, which are incorporated into a specialized expanded apical membrane, the rhabdomere. Given the extensive utilization of rhabdomeric photoreceptors in the eyes of protostomes, here we address whether a common transcriptional mechanism exists for the differentiation of rhabdomeric photoreceptors. In Drosophila, the transcription factors Pph13 and Orthodenticle (Otd) direct both aspects of differentiation: rhabdomeric opsin transcription and rhabdomere morphogenesis. We demonstrate that the orthologs of both proteins are expressed in the visual systems of the distantly related arthropod species Tribolium castaneum and Daphnia magna and that their functional roles are similar in these species. In particular, we establish that the Pph13 homologs have the ability to bind a subset of Rhodopsin core sequence I sites and that these sites are present in key phototransduction genes of both Tribolium and Daphnia. Furthermore, Pph13 and Otd orthologs are capable of executing deeply conserved functions of photoreceptor differentiation as evidenced by the ability to rescue their respective Drosophila mutant phenotypes. Pph13 homologs are equivalent in their ability to direct both rhabdomere morphogenesis and opsin expression within Drosophila, whereas Otd paralogs demonstrate differential abilities to regulate photoreceptor differentiation. Finally, loss-of-function analyses in Tribolium confirm the conserved requirement of Pph13 and Otd in regulating both rhabdomeric opsin transcription and rhabdomere morphogenesis. Taken together, our data identify components of a regulatory framework for rhabdomeric photoreceptor differentiation in Pancrustaceans, providing a foundation for defining ancestral regulatory modules of rhabdomeric photoreceptor differentiation. Public Library of Science 2014-07-03 /pmc/articles/PMC4084641/ /pubmed/24991928 http://dx.doi.org/10.1371/journal.pgen.1004484 Text en © 2014 Mahato 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
Mahato, Simpla
Morita, Shinichi
Tucker, Abraham E.
Liang, Xulong
Jackowska, Magdalena
Friedrich, Markus
Shiga, Yasuhiro
Zelhof, Andrew C.
Common Transcriptional Mechanisms for Visual Photoreceptor Cell Differentiation among Pancrustaceans
title Common Transcriptional Mechanisms for Visual Photoreceptor Cell Differentiation among Pancrustaceans
title_full Common Transcriptional Mechanisms for Visual Photoreceptor Cell Differentiation among Pancrustaceans
title_fullStr Common Transcriptional Mechanisms for Visual Photoreceptor Cell Differentiation among Pancrustaceans
title_full_unstemmed Common Transcriptional Mechanisms for Visual Photoreceptor Cell Differentiation among Pancrustaceans
title_short Common Transcriptional Mechanisms for Visual Photoreceptor Cell Differentiation among Pancrustaceans
title_sort common transcriptional mechanisms for visual photoreceptor cell differentiation among pancrustaceans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084641/
https://www.ncbi.nlm.nih.gov/pubmed/24991928
http://dx.doi.org/10.1371/journal.pgen.1004484
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