Abstract
The large number of RNA-binding proteins and translation factors encoded in the Drosophila and other metazoan genomes predicts widespread use of post-transcriptional regulation in cellular and developmental processes. Previous studies identified roles for several RNA-binding proteins in dendrite branching morphogenesis of Drosophila larval sensory neurons. To determine the larger contribution of post-transcriptional gene regulation to neuronal morphogenesis, we conducted an RNA interference screen to identify additional Drosophila proteins annotated as either RNA-binding proteins or translation factors that function in producing the complex dendritic trees of larval class IV dendritic arborization neurons. We identified 88 genes encoding such proteins whose knockdown resulted in aberrant dendritic morphology, including alterations in dendritic branch number, branch length, field size, and patterning of the dendritic tree. In particular, splicing and translation initiation factors were associated with distinct and characteristic phenotypes, suggesting that different morphogenetic events are best controlled at specific steps in post-transcriptional messenger RNA metabolism. Many of the factors identified in the screen have been implicated in controlling the subcellular distributions and translation of maternal messenger RNAs; thus, common post-transcriptional regulatory strategies may be used in neurogenesis and in the generation of asymmetry in the female germline and embryo.
Highlights
The large number of RNA-binding proteins and translation factors encoded in the Drosophila and other metazoan genomes predicts widespread use of post-transcriptional regulation in cellular and developmental processes
To better understand the role of mRNA regulatory mechanisms in dendrite morphogenesis, we investigated the functions of genes encoding RNA binding proteins (RBPs) and translational regulators in the elaboration of the dendritic branching patterns of class IV da neurons by performing a cell type-specific RNA interference (RNAi) screen
Individual upstream activating sequence (UAS)-RNAi strains obtained from the Vienna Drosophila RNAi Center (VDRC; Dietzl et al 2007), the Transgenic RNAi Project (TRiP; Harvard Medical School), and National Institute of Genetics (NIG; Japan) stock centers are listed in Supporting Information, Table S1
Summary
The large number of RNA-binding proteins and translation factors encoded in the Drosophila and other metazoan genomes predicts widespread use of post-transcriptional regulation in cellular and developmental processes. To determine the larger contribution of post-transcriptional gene regulation to neuronal morphogenesis, we conducted an RNA interference screen to identify additional Drosophila proteins annotated as either RNA-binding proteins or translation factors that function in producing the complex dendritic trees of larval class IV dendritic arborization neurons. In contrast to fmr knockout mice, Tsc2+/2 mice exhibit decreased dendritic spine numbers and decreased protein synthesis (Orlova and Crino 2010; Auerbach et al 2011; Santoro et al 2012) These findings suggest that protein synthesis must be tightly regulated for the development of dendritic structures and for the preservation of normal synaptic function. To better understand the role of mRNA regulatory mechanisms in dendrite morphogenesis, we investigated the functions of genes encoding RNA binding proteins (RBPs) and translational regulators in the elaboration of the dendritic branching patterns of class IV da neurons by performing a cell type-specific RNA interference (RNAi) screen. Common post-transcriptional regulatory strategies may be employed in neurogenesis and in the generation of asymmetry in the female germline and embryo
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.