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Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux
Monensin Sensitive 1 (Mon1) is a component of the Mon1:Ccz1 complex that mediates Rab5 to Rab7 conversion in eukaryotic cells by serving as a guanine nucleotide exchange factor for Rab7 during vesicular trafficking. We find that Mon1 activity modulates the complexity of Class IV dendritic arborizati...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687774/ https://www.ncbi.nlm.nih.gov/pubmed/31428611 http://dx.doi.org/10.3389/fcell.2019.00145 |
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author | Harish, Rohit Krishnan Tendulkar, Shweta Deivasigamani, Senthilkumar Ratnaparkhi, Anuradha Ratnaparkhi, Girish S. |
author_facet | Harish, Rohit Krishnan Tendulkar, Shweta Deivasigamani, Senthilkumar Ratnaparkhi, Anuradha Ratnaparkhi, Girish S. |
author_sort | Harish, Rohit Krishnan |
collection | PubMed |
description | Monensin Sensitive 1 (Mon1) is a component of the Mon1:Ccz1 complex that mediates Rab5 to Rab7 conversion in eukaryotic cells by serving as a guanine nucleotide exchange factor for Rab7 during vesicular trafficking. We find that Mon1 activity modulates the complexity of Class IV dendritic arborization (da) neurons during larval development. Loss of Mon1 function leads to an increase in arborization and complexity, while increased expression, leads to reduced arborization. The ability of Mon1 to influence dendritic development is possibly a function of its interactions with Rab family GTPases that are central players in vesicular trafficking. Earlier, these GTPases, specifically Rab1, Rab5, Rab10, and Rab11 have been shown to regulate dendritic arborization. We have conducted genetic epistasis experiments, by modulating the activity of Rab5, Rab7, and Rab11 in da neurons, in Mon1 mutants, and demonstrate that the ability of Mon1 to regulate arborization is possibly due to its effect on the recycling pathway. Dendritic branching is critical for proper connectivity and physiological function of the neuron. An understanding of regulatory elements, such as Mon1, as demonstrated in our study, is essential to understand neuronal function. |
format | Online Article Text |
id | pubmed-6687774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66877742019-08-19 Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux Harish, Rohit Krishnan Tendulkar, Shweta Deivasigamani, Senthilkumar Ratnaparkhi, Anuradha Ratnaparkhi, Girish S. Front Cell Dev Biol Cell and Developmental Biology Monensin Sensitive 1 (Mon1) is a component of the Mon1:Ccz1 complex that mediates Rab5 to Rab7 conversion in eukaryotic cells by serving as a guanine nucleotide exchange factor for Rab7 during vesicular trafficking. We find that Mon1 activity modulates the complexity of Class IV dendritic arborization (da) neurons during larval development. Loss of Mon1 function leads to an increase in arborization and complexity, while increased expression, leads to reduced arborization. The ability of Mon1 to influence dendritic development is possibly a function of its interactions with Rab family GTPases that are central players in vesicular trafficking. Earlier, these GTPases, specifically Rab1, Rab5, Rab10, and Rab11 have been shown to regulate dendritic arborization. We have conducted genetic epistasis experiments, by modulating the activity of Rab5, Rab7, and Rab11 in da neurons, in Mon1 mutants, and demonstrate that the ability of Mon1 to regulate arborization is possibly due to its effect on the recycling pathway. Dendritic branching is critical for proper connectivity and physiological function of the neuron. An understanding of regulatory elements, such as Mon1, as demonstrated in our study, is essential to understand neuronal function. Frontiers Media S.A. 2019-08-02 /pmc/articles/PMC6687774/ /pubmed/31428611 http://dx.doi.org/10.3389/fcell.2019.00145 Text en Copyright © 2019 Harish, Tendulkar, Deivasigamani, Ratnaparkhi and Ratnaparkhi. 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 | Cell and Developmental Biology Harish, Rohit Krishnan Tendulkar, Shweta Deivasigamani, Senthilkumar Ratnaparkhi, Anuradha Ratnaparkhi, Girish S. Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux |
title | Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux |
title_full | Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux |
title_fullStr | Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux |
title_full_unstemmed | Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux |
title_short | Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux |
title_sort | monensin sensitive 1 regulates dendritic arborization in drosophila by modulating endocytic flux |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687774/ https://www.ncbi.nlm.nih.gov/pubmed/31428611 http://dx.doi.org/10.3389/fcell.2019.00145 |
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