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The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function

Pax6 and its Drosophila homolog Eyeless (Ey) play essential roles during eye development. Ey/Pax6 contains two distinct DNA binding domains, a Paired domain (PD) and a Homeodomain (HD). While Ey/Pax6 PD is required for the expression of key regulators of retinal development, relatively little is kno...

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Autores principales: Tanaka-Matakatsu, Miho, Miller, John, Du, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Higher Education Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286722/
https://www.ncbi.nlm.nih.gov/pubmed/25234589
http://dx.doi.org/10.1007/s13238-014-0101-9
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author Tanaka-Matakatsu, Miho
Miller, John
Du, Wei
author_facet Tanaka-Matakatsu, Miho
Miller, John
Du, Wei
author_sort Tanaka-Matakatsu, Miho
collection PubMed
description Pax6 and its Drosophila homolog Eyeless (Ey) play essential roles during eye development. Ey/Pax6 contains two distinct DNA binding domains, a Paired domain (PD) and a Homeodomain (HD). While Ey/Pax6 PD is required for the expression of key regulators of retinal development, relatively little is known about the HD-dependent Ey function. In this study, we used the UAS/GAL4 system to determine the functions of different Ey domains on cell growth and on retinal development. We showed that Ey can promote cell growth, which requires the HD but not the PD. In contrast, the ability of Ey to activate Ato expression and induce ectopic eye formation requires the PD but not the HD. Interestingly, deletion of the HD enhanced Ey-dependent ectopic eye induction while overexpression of the HD only Ey forms antagonizes ectopic eye induction. These studies revealed a novel function of Ey HD on cell growth and a novel antagonistic effect of Ey HD on Ey PD-dependent eye induction. We further show the third helix of the Ey HD can directly interact with the RED subdomain in Ey PD and that deletion of the HD increased the binding of Ey PD to its target. These results suggest that the direct interaction between the HD and the PD potentially mediates their antagonistic effects. Since different Ey splicing forms are expressed in overlapping regions during normal development, we speculate that the expression ratios of the different Ey splice forms potentially contribute to the regulation of growth and differentiation of these tissues. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13238-014-0101-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-42867222015-01-15 The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function Tanaka-Matakatsu, Miho Miller, John Du, Wei Protein Cell Research Article Pax6 and its Drosophila homolog Eyeless (Ey) play essential roles during eye development. Ey/Pax6 contains two distinct DNA binding domains, a Paired domain (PD) and a Homeodomain (HD). While Ey/Pax6 PD is required for the expression of key regulators of retinal development, relatively little is known about the HD-dependent Ey function. In this study, we used the UAS/GAL4 system to determine the functions of different Ey domains on cell growth and on retinal development. We showed that Ey can promote cell growth, which requires the HD but not the PD. In contrast, the ability of Ey to activate Ato expression and induce ectopic eye formation requires the PD but not the HD. Interestingly, deletion of the HD enhanced Ey-dependent ectopic eye induction while overexpression of the HD only Ey forms antagonizes ectopic eye induction. These studies revealed a novel function of Ey HD on cell growth and a novel antagonistic effect of Ey HD on Ey PD-dependent eye induction. We further show the third helix of the Ey HD can directly interact with the RED subdomain in Ey PD and that deletion of the HD increased the binding of Ey PD to its target. These results suggest that the direct interaction between the HD and the PD potentially mediates their antagonistic effects. Since different Ey splicing forms are expressed in overlapping regions during normal development, we speculate that the expression ratios of the different Ey splice forms potentially contribute to the regulation of growth and differentiation of these tissues. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13238-014-0101-9) contains supplementary material, which is available to authorized users. Higher Education Press 2014-09-20 2015-01 /pmc/articles/PMC4286722/ /pubmed/25234589 http://dx.doi.org/10.1007/s13238-014-0101-9 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research Article
Tanaka-Matakatsu, Miho
Miller, John
Du, Wei
The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function
title The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function
title_full The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function
title_fullStr The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function
title_full_unstemmed The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function
title_short The homeodomain of Eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function
title_sort homeodomain of eyeless regulates cell growth and antagonizes the paired domain-dependent retinal differentiation function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286722/
https://www.ncbi.nlm.nih.gov/pubmed/25234589
http://dx.doi.org/10.1007/s13238-014-0101-9
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