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The potential role of Arhgef33 RhoGEF in foveal development in the zebra finch retina

The fovea is a pit formed in the center of the retina that enables high-acuity vision in certain vertebrate species. While formation of the fovea fascinates many researchers, the molecular mechanisms underlying foveal development are poorly understood. In the current study, we histologically investi...

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Autores principales: Sugiyama, Takefumi, Yamamoto, Haruka, Kon, Tetsuo, Chaya, Taro, Omori, Yoshihiro, Suzuki, Yutaka, Abe, Kentaro, Watanabe, Dai, Furukawa, Takahisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722920/
https://www.ncbi.nlm.nih.gov/pubmed/33293601
http://dx.doi.org/10.1038/s41598-020-78452-6
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author Sugiyama, Takefumi
Yamamoto, Haruka
Kon, Tetsuo
Chaya, Taro
Omori, Yoshihiro
Suzuki, Yutaka
Abe, Kentaro
Watanabe, Dai
Furukawa, Takahisa
author_facet Sugiyama, Takefumi
Yamamoto, Haruka
Kon, Tetsuo
Chaya, Taro
Omori, Yoshihiro
Suzuki, Yutaka
Abe, Kentaro
Watanabe, Dai
Furukawa, Takahisa
author_sort Sugiyama, Takefumi
collection PubMed
description The fovea is a pit formed in the center of the retina that enables high-acuity vision in certain vertebrate species. While formation of the fovea fascinates many researchers, the molecular mechanisms underlying foveal development are poorly understood. In the current study, we histologically investigated foveal development in zebra finch (Taeniopygia guttata) and found that foveal pit formation begins just before post-hatch day 14 (P14). We next performed RNA-seq analysis to compare gene expression profiles between the central (foveal and parafoveal) and peripheral retina in zebra finch at P14. We found that the Arhgef33 expression is enriched in the middle layer of the inner nuclear layer at the parafovea, suggesting that Arhgef33 is dominantly expressed in Müller glial cells in the developing parafovea. We then performed a pull-down assay using Rhotekin-RBD and observed GEF activity of Arhgef33 against RhoA. We found that overexpression of Arhgef33 in HEK293 cells induces cell contraction and that Arhgef33 expression inhibits neurite extension in Neuro 2A cells, which is partially recovered by a Rho-kinase (ROCK) inhibitor. Taken together, we used zebra finch as a model animal to investigate foveal development and identified Arhgef33 as a candidate protein possibly involved in foveal development through modulating RhoA activity.
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spelling pubmed-77229202020-12-09 The potential role of Arhgef33 RhoGEF in foveal development in the zebra finch retina Sugiyama, Takefumi Yamamoto, Haruka Kon, Tetsuo Chaya, Taro Omori, Yoshihiro Suzuki, Yutaka Abe, Kentaro Watanabe, Dai Furukawa, Takahisa Sci Rep Article The fovea is a pit formed in the center of the retina that enables high-acuity vision in certain vertebrate species. While formation of the fovea fascinates many researchers, the molecular mechanisms underlying foveal development are poorly understood. In the current study, we histologically investigated foveal development in zebra finch (Taeniopygia guttata) and found that foveal pit formation begins just before post-hatch day 14 (P14). We next performed RNA-seq analysis to compare gene expression profiles between the central (foveal and parafoveal) and peripheral retina in zebra finch at P14. We found that the Arhgef33 expression is enriched in the middle layer of the inner nuclear layer at the parafovea, suggesting that Arhgef33 is dominantly expressed in Müller glial cells in the developing parafovea. We then performed a pull-down assay using Rhotekin-RBD and observed GEF activity of Arhgef33 against RhoA. We found that overexpression of Arhgef33 in HEK293 cells induces cell contraction and that Arhgef33 expression inhibits neurite extension in Neuro 2A cells, which is partially recovered by a Rho-kinase (ROCK) inhibitor. Taken together, we used zebra finch as a model animal to investigate foveal development and identified Arhgef33 as a candidate protein possibly involved in foveal development through modulating RhoA activity. Nature Publishing Group UK 2020-12-08 /pmc/articles/PMC7722920/ /pubmed/33293601 http://dx.doi.org/10.1038/s41598-020-78452-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sugiyama, Takefumi
Yamamoto, Haruka
Kon, Tetsuo
Chaya, Taro
Omori, Yoshihiro
Suzuki, Yutaka
Abe, Kentaro
Watanabe, Dai
Furukawa, Takahisa
The potential role of Arhgef33 RhoGEF in foveal development in the zebra finch retina
title The potential role of Arhgef33 RhoGEF in foveal development in the zebra finch retina
title_full The potential role of Arhgef33 RhoGEF in foveal development in the zebra finch retina
title_fullStr The potential role of Arhgef33 RhoGEF in foveal development in the zebra finch retina
title_full_unstemmed The potential role of Arhgef33 RhoGEF in foveal development in the zebra finch retina
title_short The potential role of Arhgef33 RhoGEF in foveal development in the zebra finch retina
title_sort potential role of arhgef33 rhogef in foveal development in the zebra finch retina
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722920/
https://www.ncbi.nlm.nih.gov/pubmed/33293601
http://dx.doi.org/10.1038/s41598-020-78452-6
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