Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Lai, Yen-Wei, Chu, Sao-Yu, Li, Jian-Chiuan, Chen, Po-Lin, Chen, Chun-Hong, Yu, Hung-Hsiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
_version_ 1783508609117716480
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
work_keys_str_mv AT laiyenwei visualizationofendogenoustypeitgfbreceptorbabooninthedrosophilabrain
AT chusaoyu visualizationofendogenoustypeitgfbreceptorbabooninthedrosophilabrain
AT lijianchiuan visualizationofendogenoustypeitgfbreceptorbabooninthedrosophilabrain
AT chenpolin visualizationofendogenoustypeitgfbreceptorbabooninthedrosophilabrain
AT chenchunhong visualizationofendogenoustypeitgfbreceptorbabooninthedrosophilabrain
AT yuhunghsiang visualizationofendogenoustypeitgfbreceptorbabooninthedrosophilabrain