RNA interference screen to identify genes required for Drosophila embryonic nervous system development
Open Access
- 27 March 2007
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 104 (13) , 5626-5631
- https://doi.org/10.1073/pnas.0611687104
Abstract
RNA interference (RNAi) has been shown to be a powerful method to study the function of genes in vivo by silencing endogenous mRNA with double-stranded (ds) RNA. Previously, we performed in vivo RNAi screening and identified 43 Drosophila genes, including 18 novel genes required for the development of the embryonic nervous system. In the present study, 22 additional genes affecting embryonic nervous system development were found. Novel RNAi-induced phenotypes affecting nervous system development were found for 16 of the 22 genes. Seven of the genes have unknown functions. Other genes found encode transcription factors, a chromatin-remodeling protein, membrane receptors, signaling molecules, and proteins involved in cell adhesion, RNA binding, and ion transport. Human orthologs were identified for proteins encoded by 16 of the genes. The total number of dsRNAs that we have tested for an RNAi-induced phenotype affecting the embryonic nervous system, including our previous study, is 7,312, which corresponds to ≈50% of the genes in the Drosophila genome.Keywords
This publication has 61 references indexed in Scilit:
- Expression of the Rho-GEF Pbl/ECT2 is regulated by the UBE3A E3 ubiquitin ligaseHuman Molecular Genetics, 2006
- Genome-wide RNAi screen of Ca 2+ influx identifies genes that regulate Ca 2+ release-activated Ca 2+ channel activityProceedings of the National Academy of Sciences, 2006
- Genome-wide high-throughput screens in functional genomicsCurrent Opinion in Genetics & Development, 2004
- Acf1 confers unique activities to ACF/CHRAC and promotes the formation rather than disruption of chromatin in vivoGenes & Development, 2004
- RNA interferenceNature, 2002
- Adherens junctions inhibit asymmetric division in the Drosophila epitheliumNature, 2001
- Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domainNature Genetics, 1997
- Drosophila α-Catenin and E-cadherin Bind to Distinct Regions of Drosophila ArmadilloJournal of Biological Chemistry, 1996
- Separation of Sister Chromatids in Mitosis Requires the Drosophila pimples Product, a Protein Degraded after the Metaphase/Anaphase TransitionCell, 1996
- Cloning of the Drosophila prospero gene and its expression in ganglion mother cellsBiochemical and Biophysical Research Communications, 1992