Cargando…

A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation

Drosophila rhabdomeric terminal photoreceptor differentiation is an extended process taking several days to complete. Following ommatidial patterning by the morphogenetic furrow, photoreceptors are sequentially recruited and specified, and terminal differentiation begins. Key events of terminal diff...

Descripción completa

Detalles Bibliográficos
Autores principales: Rylee, Johnathan, Mahato, Simpla, Aldrich, John, Bergh, Emma, Sizemore, Brandon, Feder, Lauren E, Grega, Shaun, Helms, Kennedy, Maar, Megan, Britt, Steven G, Zelhof, Andrew C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635655/
https://www.ncbi.nlm.nih.gov/pubmed/36218412
http://dx.doi.org/10.1093/g3journal/jkac257
_version_ 1784824756051116032
author Rylee, Johnathan
Mahato, Simpla
Aldrich, John
Bergh, Emma
Sizemore, Brandon
Feder, Lauren E
Grega, Shaun
Helms, Kennedy
Maar, Megan
Britt, Steven G
Zelhof, Andrew C
author_facet Rylee, Johnathan
Mahato, Simpla
Aldrich, John
Bergh, Emma
Sizemore, Brandon
Feder, Lauren E
Grega, Shaun
Helms, Kennedy
Maar, Megan
Britt, Steven G
Zelhof, Andrew C
author_sort Rylee, Johnathan
collection PubMed
description Drosophila rhabdomeric terminal photoreceptor differentiation is an extended process taking several days to complete. Following ommatidial patterning by the morphogenetic furrow, photoreceptors are sequentially recruited and specified, and terminal differentiation begins. Key events of terminal differentiation include the establishment of apical and basolateral domains, rhabdomere and stalk formation, inter-rhabdomeral space formation, and expression of phototransduction machinery. While many key regulators of these processes have been identified, the complete network of transcription factors to downstream effector molecules necessary for regulating each of these major events remains incomplete. Here, we report an RNAi screen to identify additional molecules and cellular pathways required for photoreceptor terminal differentiation. First, we tested several eye-specific GAL4 drivers for correct spatial and temporal specificity and identified Pph13-GAL4 as the most appropriate GAL4 line for our screen. We screened lines available through the Transgenic RNAi Project and isolated lines that when combined with Pph13-GAL4 resulted in the loss of the deep pseudopupil, as a readout for abnormal differentiation. In the end, we screened 6,189 lines, representing 3,971 genes, and have identified 64 genes, illuminating potential new regulatory molecules and cellular pathways for the differentiation and organization of Drosophila rhabdomeric photoreceptors.
format Online
Article
Text
id pubmed-9635655
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-96356552022-11-07 A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation Rylee, Johnathan Mahato, Simpla Aldrich, John Bergh, Emma Sizemore, Brandon Feder, Lauren E Grega, Shaun Helms, Kennedy Maar, Megan Britt, Steven G Zelhof, Andrew C G3 (Bethesda) Mutant Screen Report Drosophila rhabdomeric terminal photoreceptor differentiation is an extended process taking several days to complete. Following ommatidial patterning by the morphogenetic furrow, photoreceptors are sequentially recruited and specified, and terminal differentiation begins. Key events of terminal differentiation include the establishment of apical and basolateral domains, rhabdomere and stalk formation, inter-rhabdomeral space formation, and expression of phototransduction machinery. While many key regulators of these processes have been identified, the complete network of transcription factors to downstream effector molecules necessary for regulating each of these major events remains incomplete. Here, we report an RNAi screen to identify additional molecules and cellular pathways required for photoreceptor terminal differentiation. First, we tested several eye-specific GAL4 drivers for correct spatial and temporal specificity and identified Pph13-GAL4 as the most appropriate GAL4 line for our screen. We screened lines available through the Transgenic RNAi Project and isolated lines that when combined with Pph13-GAL4 resulted in the loss of the deep pseudopupil, as a readout for abnormal differentiation. In the end, we screened 6,189 lines, representing 3,971 genes, and have identified 64 genes, illuminating potential new regulatory molecules and cellular pathways for the differentiation and organization of Drosophila rhabdomeric photoreceptors. Oxford University Press 2022-10-11 /pmc/articles/PMC9635655/ /pubmed/36218412 http://dx.doi.org/10.1093/g3journal/jkac257 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Mutant Screen Report
Rylee, Johnathan
Mahato, Simpla
Aldrich, John
Bergh, Emma
Sizemore, Brandon
Feder, Lauren E
Grega, Shaun
Helms, Kennedy
Maar, Megan
Britt, Steven G
Zelhof, Andrew C
A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation
title A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation
title_full A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation
title_fullStr A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation
title_full_unstemmed A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation
title_short A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation
title_sort trip rnai screen to identify molecules necessary for drosophila photoreceptor differentiation
topic Mutant Screen Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635655/
https://www.ncbi.nlm.nih.gov/pubmed/36218412
http://dx.doi.org/10.1093/g3journal/jkac257
work_keys_str_mv AT ryleejohnathan atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT mahatosimpla atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT aldrichjohn atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT berghemma atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT sizemorebrandon atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT federlaurene atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT gregashaun atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT helmskennedy atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT maarmegan atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT brittsteveng atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT zelhofandrewc atriprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT ryleejohnathan triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT mahatosimpla triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT aldrichjohn triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT berghemma triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT sizemorebrandon triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT federlaurene triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT gregashaun triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT helmskennedy triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT maarmegan triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT brittsteveng triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation
AT zelhofandrewc triprnaiscreentoidentifymoleculesnecessaryfordrosophilaphotoreceptordifferentiation