Cargando…

RNAi-Mediated Reverse Genetic Screen Identified Drosophila Chaperones Regulating Eye and Neuromuscular Junction Morphology

Accumulation of toxic proteins in neurons has been linked with the onset of neurodegenerative diseases, which in many cases are characterized by altered neuronal function and synapse loss. Molecular chaperones help protein folding and the resolubilization of unfolded proteins, thereby reducing the p...

Descripción completa

Detalles Bibliográficos
Autores principales: Raut, Sandeep, Mallik, Bhagaban, Parichha, Arpan, Amrutha, Valsakumar, Sahi, Chandan, Kumar, Vimlesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499113/
https://www.ncbi.nlm.nih.gov/pubmed/28500055
http://dx.doi.org/10.1534/g3.117.041632
_version_ 1783248417667940352
author Raut, Sandeep
Mallik, Bhagaban
Parichha, Arpan
Amrutha, Valsakumar
Sahi, Chandan
Kumar, Vimlesh
author_facet Raut, Sandeep
Mallik, Bhagaban
Parichha, Arpan
Amrutha, Valsakumar
Sahi, Chandan
Kumar, Vimlesh
author_sort Raut, Sandeep
collection PubMed
description Accumulation of toxic proteins in neurons has been linked with the onset of neurodegenerative diseases, which in many cases are characterized by altered neuronal function and synapse loss. Molecular chaperones help protein folding and the resolubilization of unfolded proteins, thereby reducing the protein aggregation stress. While most of the chaperones are expressed in neurons, their functional relevance remains largely unknown. Here, using bioinformatics analysis, we identified 95 Drosophila chaperones and classified them into seven different classes. Ubiquitous actin5C-Gal4-mediated RNAi knockdown revealed that ∼50% of the chaperones are essential in Drosophila. Knocking down these genes in eyes revealed that ∼30% of the essential chaperones are crucial for eye development. Using neuron-specific knockdown, immunocytochemistry, and robust behavioral assays, we identified a new set of chaperones that play critical roles in the regulation of Drosophila NMJ structural organization. Together, our data present the first classification and comprehensive analysis of Drosophila chaperones. Our screen identified a new set of chaperones that regulate eye and NMJ morphogenesis. The outcome of the screen reported here provides a useful resource for further elucidating the role of individual chaperones in Drosophila eye morphogenesis and synaptic development.
format Online
Article
Text
id pubmed-5499113
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Genetics Society of America
record_format MEDLINE/PubMed
spelling pubmed-54991132017-07-07 RNAi-Mediated Reverse Genetic Screen Identified Drosophila Chaperones Regulating Eye and Neuromuscular Junction Morphology Raut, Sandeep Mallik, Bhagaban Parichha, Arpan Amrutha, Valsakumar Sahi, Chandan Kumar, Vimlesh G3 (Bethesda) Mutant Screen Report Accumulation of toxic proteins in neurons has been linked with the onset of neurodegenerative diseases, which in many cases are characterized by altered neuronal function and synapse loss. Molecular chaperones help protein folding and the resolubilization of unfolded proteins, thereby reducing the protein aggregation stress. While most of the chaperones are expressed in neurons, their functional relevance remains largely unknown. Here, using bioinformatics analysis, we identified 95 Drosophila chaperones and classified them into seven different classes. Ubiquitous actin5C-Gal4-mediated RNAi knockdown revealed that ∼50% of the chaperones are essential in Drosophila. Knocking down these genes in eyes revealed that ∼30% of the essential chaperones are crucial for eye development. Using neuron-specific knockdown, immunocytochemistry, and robust behavioral assays, we identified a new set of chaperones that play critical roles in the regulation of Drosophila NMJ structural organization. Together, our data present the first classification and comprehensive analysis of Drosophila chaperones. Our screen identified a new set of chaperones that regulate eye and NMJ morphogenesis. The outcome of the screen reported here provides a useful resource for further elucidating the role of individual chaperones in Drosophila eye morphogenesis and synaptic development. Genetics Society of America 2017-05-08 /pmc/articles/PMC5499113/ /pubmed/28500055 http://dx.doi.org/10.1534/g3.117.041632 Text en Copyright © 2017 Raut et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Mutant Screen Report
Raut, Sandeep
Mallik, Bhagaban
Parichha, Arpan
Amrutha, Valsakumar
Sahi, Chandan
Kumar, Vimlesh
RNAi-Mediated Reverse Genetic Screen Identified Drosophila Chaperones Regulating Eye and Neuromuscular Junction Morphology
title RNAi-Mediated Reverse Genetic Screen Identified Drosophila Chaperones Regulating Eye and Neuromuscular Junction Morphology
title_full RNAi-Mediated Reverse Genetic Screen Identified Drosophila Chaperones Regulating Eye and Neuromuscular Junction Morphology
title_fullStr RNAi-Mediated Reverse Genetic Screen Identified Drosophila Chaperones Regulating Eye and Neuromuscular Junction Morphology
title_full_unstemmed RNAi-Mediated Reverse Genetic Screen Identified Drosophila Chaperones Regulating Eye and Neuromuscular Junction Morphology
title_short RNAi-Mediated Reverse Genetic Screen Identified Drosophila Chaperones Regulating Eye and Neuromuscular Junction Morphology
title_sort rnai-mediated reverse genetic screen identified drosophila chaperones regulating eye and neuromuscular junction morphology
topic Mutant Screen Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499113/
https://www.ncbi.nlm.nih.gov/pubmed/28500055
http://dx.doi.org/10.1534/g3.117.041632
work_keys_str_mv AT rautsandeep rnaimediatedreversegeneticscreenidentifieddrosophilachaperonesregulatingeyeandneuromuscularjunctionmorphology
AT mallikbhagaban rnaimediatedreversegeneticscreenidentifieddrosophilachaperonesregulatingeyeandneuromuscularjunctionmorphology
AT parichhaarpan rnaimediatedreversegeneticscreenidentifieddrosophilachaperonesregulatingeyeandneuromuscularjunctionmorphology
AT amruthavalsakumar rnaimediatedreversegeneticscreenidentifieddrosophilachaperonesregulatingeyeandneuromuscularjunctionmorphology
AT sahichandan rnaimediatedreversegeneticscreenidentifieddrosophilachaperonesregulatingeyeandneuromuscularjunctionmorphology
AT kumarvimlesh rnaimediatedreversegeneticscreenidentifieddrosophilachaperonesregulatingeyeandneuromuscularjunctionmorphology