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Investigation of Isoform Specific Functions of the V-ATPase a Subunit During Drosophila Wing Development

The vacuolar ATPases (V-ATPases) are ATP-dependent proton pumps that play vital roles in eukaryotic cells. Insect V-ATPases are required in nearly all epithelial tissues to regulate a multiplicity of processes including receptor-mediated endocytosis, protein degradation, fluid secretion, and neurotr...

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Autores principales: Mo, Dongqing, Chen, Yao, Jiang, Na, Shen, Jie, Zhang, Junzheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365883/
https://www.ncbi.nlm.nih.gov/pubmed/32754202
http://dx.doi.org/10.3389/fgene.2020.00723
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author Mo, Dongqing
Chen, Yao
Jiang, Na
Shen, Jie
Zhang, Junzheng
author_facet Mo, Dongqing
Chen, Yao
Jiang, Na
Shen, Jie
Zhang, Junzheng
author_sort Mo, Dongqing
collection PubMed
description The vacuolar ATPases (V-ATPases) are ATP-dependent proton pumps that play vital roles in eukaryotic cells. Insect V-ATPases are required in nearly all epithelial tissues to regulate a multiplicity of processes including receptor-mediated endocytosis, protein degradation, fluid secretion, and neurotransmission. Composed of fourteen different subunits, several V-ATPase subunits exist in distinct isoforms to perform cell type specific functions. The 100 kD a subunit (Vha100) of V-ATPases are encoded by a family of five genes in Drosophila, but their assignments are not fully understood. Here we report an experimental survey of the Vha100 gene family during Drosophila wing development. A combination of CRISPR-Cas9 mutagenesis, somatic clonal analysis and in vivo RNAi assays is used to characterize the requirement of Vha100 isoforms, and mutants of Vha100-2, Vha100-3, Vha100-4, and Vha100-5 genes were generated. We show that Vha100-3 and Vha100-5 are dispensable for fly development, while Vha100-1 is not critically required in the wing. As for the other two isoforms, we find that Vha100-2 regulates wing cuticle maturation, while Vha100-4 is the single isoform involved in developmental patterning. More specifically, Vha100-4 is required for proper activation of the Wingless signaling pathway during fly wing development. Interestingly, we also find a specific genetic interaction between Vha100-1 and Vha100-4 during wing development. Our results revealed the distinct roles of Vha100 isoforms during insect wing development, providing a rationale for understanding the diverse roles of V-ATPases.
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spelling pubmed-73658832020-08-03 Investigation of Isoform Specific Functions of the V-ATPase a Subunit During Drosophila Wing Development Mo, Dongqing Chen, Yao Jiang, Na Shen, Jie Zhang, Junzheng Front Genet Genetics The vacuolar ATPases (V-ATPases) are ATP-dependent proton pumps that play vital roles in eukaryotic cells. Insect V-ATPases are required in nearly all epithelial tissues to regulate a multiplicity of processes including receptor-mediated endocytosis, protein degradation, fluid secretion, and neurotransmission. Composed of fourteen different subunits, several V-ATPase subunits exist in distinct isoforms to perform cell type specific functions. The 100 kD a subunit (Vha100) of V-ATPases are encoded by a family of five genes in Drosophila, but their assignments are not fully understood. Here we report an experimental survey of the Vha100 gene family during Drosophila wing development. A combination of CRISPR-Cas9 mutagenesis, somatic clonal analysis and in vivo RNAi assays is used to characterize the requirement of Vha100 isoforms, and mutants of Vha100-2, Vha100-3, Vha100-4, and Vha100-5 genes were generated. We show that Vha100-3 and Vha100-5 are dispensable for fly development, while Vha100-1 is not critically required in the wing. As for the other two isoforms, we find that Vha100-2 regulates wing cuticle maturation, while Vha100-4 is the single isoform involved in developmental patterning. More specifically, Vha100-4 is required for proper activation of the Wingless signaling pathway during fly wing development. Interestingly, we also find a specific genetic interaction between Vha100-1 and Vha100-4 during wing development. Our results revealed the distinct roles of Vha100 isoforms during insect wing development, providing a rationale for understanding the diverse roles of V-ATPases. Frontiers Media S.A. 2020-07-10 /pmc/articles/PMC7365883/ /pubmed/32754202 http://dx.doi.org/10.3389/fgene.2020.00723 Text en Copyright © 2020 Mo, Chen, Jiang, Shen and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Mo, Dongqing
Chen, Yao
Jiang, Na
Shen, Jie
Zhang, Junzheng
Investigation of Isoform Specific Functions of the V-ATPase a Subunit During Drosophila Wing Development
title Investigation of Isoform Specific Functions of the V-ATPase a Subunit During Drosophila Wing Development
title_full Investigation of Isoform Specific Functions of the V-ATPase a Subunit During Drosophila Wing Development
title_fullStr Investigation of Isoform Specific Functions of the V-ATPase a Subunit During Drosophila Wing Development
title_full_unstemmed Investigation of Isoform Specific Functions of the V-ATPase a Subunit During Drosophila Wing Development
title_short Investigation of Isoform Specific Functions of the V-ATPase a Subunit During Drosophila Wing Development
title_sort investigation of isoform specific functions of the v-atpase a subunit during drosophila wing development
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365883/
https://www.ncbi.nlm.nih.gov/pubmed/32754202
http://dx.doi.org/10.3389/fgene.2020.00723
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