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Visualization of Endogenous Type I TGF-β Receptor Baboon in the Drosophila Brain
The transforming growth factor β (TGF-β) signaling pathway is evolutionarily conserved and widely used in the animal kingdom to regulate diverse developmental processes. Prior studies have shown that Baboon (Babo), a Drosophila type I TGF-β receptor, plays essential roles in brain development and ne...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083856/ https://www.ncbi.nlm.nih.gov/pubmed/32198477 http://dx.doi.org/10.1038/s41598-020-61950-y |
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author | Lai, Yen-Wei Chu, Sao-Yu Li, Jian-Chiuan Chen, Po-Lin Chen, Chun-Hong Yu, Hung-Hsiang |
author_facet | Lai, Yen-Wei Chu, Sao-Yu Li, Jian-Chiuan Chen, Po-Lin Chen, Chun-Hong Yu, Hung-Hsiang |
author_sort | Lai, Yen-Wei |
collection | PubMed |
description | The transforming growth factor β (TGF-β) signaling pathway is evolutionarily conserved and widely used in the animal kingdom to regulate diverse developmental processes. Prior studies have shown that Baboon (Babo), a Drosophila type I TGF-β receptor, plays essential roles in brain development and neural circuit formation. However, the expression pattern for Babo in the developing brain has not been previously reported. We generated a knock-in fly with a human influenza hemagglutinin (HA) tag at the C-terminus of Babo and assessed its localization. Babo::HA was primarily expressed in brain structures enriched with neurites, including the mushroom body lobe and neuropils of the optic lobe, where Babo has been shown to instruct neuronal morphogenesis. Since the babo 3' untranslated region contains a predicted microRNA-34 (miR-34) target sequence, we further tested whether Babo::HA expression was affected by modulating the level of miR-34. We found that Babo was upregulated by mir-34 deletion and downregulated by miR-34 overexpression, confirming that it is indeed a miR-34 target gene. Taken together, our results demonstrate that the babo(HA) fly permits accurate visualization of endogenous Babo expression during brain development and the construction of functional neural circuits. |
format | Online Article Text |
id | pubmed-7083856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70838562020-03-26 Visualization of Endogenous Type I TGF-β Receptor Baboon in the Drosophila Brain Lai, Yen-Wei Chu, Sao-Yu Li, Jian-Chiuan Chen, Po-Lin Chen, Chun-Hong Yu, Hung-Hsiang Sci Rep Article The transforming growth factor β (TGF-β) signaling pathway is evolutionarily conserved and widely used in the animal kingdom to regulate diverse developmental processes. Prior studies have shown that Baboon (Babo), a Drosophila type I TGF-β receptor, plays essential roles in brain development and neural circuit formation. However, the expression pattern for Babo in the developing brain has not been previously reported. We generated a knock-in fly with a human influenza hemagglutinin (HA) tag at the C-terminus of Babo and assessed its localization. Babo::HA was primarily expressed in brain structures enriched with neurites, including the mushroom body lobe and neuropils of the optic lobe, where Babo has been shown to instruct neuronal morphogenesis. Since the babo 3' untranslated region contains a predicted microRNA-34 (miR-34) target sequence, we further tested whether Babo::HA expression was affected by modulating the level of miR-34. We found that Babo was upregulated by mir-34 deletion and downregulated by miR-34 overexpression, confirming that it is indeed a miR-34 target gene. Taken together, our results demonstrate that the babo(HA) fly permits accurate visualization of endogenous Babo expression during brain development and the construction of functional neural circuits. Nature Publishing Group UK 2020-03-20 /pmc/articles/PMC7083856/ /pubmed/32198477 http://dx.doi.org/10.1038/s41598-020-61950-y 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lai, Yen-Wei Chu, Sao-Yu Li, Jian-Chiuan Chen, Po-Lin Chen, Chun-Hong Yu, Hung-Hsiang Visualization of Endogenous Type I TGF-β Receptor Baboon in the Drosophila Brain |
title | Visualization of Endogenous Type I TGF-β Receptor Baboon in the Drosophila Brain |
title_full | Visualization of Endogenous Type I TGF-β Receptor Baboon in the Drosophila Brain |
title_fullStr | Visualization of Endogenous Type I TGF-β Receptor Baboon in the Drosophila Brain |
title_full_unstemmed | Visualization of Endogenous Type I TGF-β Receptor Baboon in the Drosophila Brain |
title_short | Visualization of Endogenous Type I TGF-β Receptor Baboon in the Drosophila Brain |
title_sort | visualization of endogenous type i tgf-β receptor baboon in the drosophila brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083856/ https://www.ncbi.nlm.nih.gov/pubmed/32198477 http://dx.doi.org/10.1038/s41598-020-61950-y |
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