GenomeRNAi - a database for RNAi phenotypes and reagents

Phenotype information for gene 3772719 (CG33964)

Screen TitleGene IDGene SymbolReagent IDScorePhenotypeFollow Up
Notch pathway regulation (4)
CG33964|CG13175
2 Loss of bristles no

Reference

Genome-wide analysis of Notch signalling in Drosophila by transgenic RNAi. Mummery-Widmer et al., 2009

Genome-wide RNA interference (RNAi) screens have identified near-complete sets of genes involved in cellular processes. However, this methodology has not yet been used to study complex developmental processes in a tissue-specific manner. Here we report the use of a library of Drosophila strains expressing inducible hairpin RNAi constructs to study the Notch signalling pathway during external sensory organ development. We assigned putative loss-of-function phenotypes to 21.2% of the protein-coding Drosophila genes. Using secondary assays, we identified 6 new genes involved in asymmetric cell division and 23 novel genes regulating the Notch signalling pathway. By integrating our phenotypic results with protein interaction data, we constructed a genome-wide, functionally validated interaction network governing Notch signalling and asymmetric cell division. We used clustering algorithms to identify nuclear import pathways and the COP9 signallosome as Notch regulators. Our results show that complex developmental processes can be analysed on a genome-wide level and provide a unique resource for functional annotation of the Drosophila genome.

Screen details

Stable Id: GR00144-A-4
Screen title: Notch pathway regulation (4)
Assay: External sensory organ morphology and viability
Method: Visual inspection
Scope: Genome-wide
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Tissue
Biomodel: pnr-GAL4
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: Phenotype strength
Cutoff: np
Notes:

Notch pathway regulation (4)
CG33964|CG13175
1 Loss of bristles no

Reference

Genome-wide analysis of Notch signalling in Drosophila by transgenic RNAi. Mummery-Widmer et al., 2009

Genome-wide RNA interference (RNAi) screens have identified near-complete sets of genes involved in cellular processes. However, this methodology has not yet been used to study complex developmental processes in a tissue-specific manner. Here we report the use of a library of Drosophila strains expressing inducible hairpin RNAi constructs to study the Notch signalling pathway during external sensory organ development. We assigned putative loss-of-function phenotypes to 21.2% of the protein-coding Drosophila genes. Using secondary assays, we identified 6 new genes involved in asymmetric cell division and 23 novel genes regulating the Notch signalling pathway. By integrating our phenotypic results with protein interaction data, we constructed a genome-wide, functionally validated interaction network governing Notch signalling and asymmetric cell division. We used clustering algorithms to identify nuclear import pathways and the COP9 signallosome as Notch regulators. Our results show that complex developmental processes can be analysed on a genome-wide level and provide a unique resource for functional annotation of the Drosophila genome.

Screen details

Stable Id: GR00144-A-4
Screen title: Notch pathway regulation (4)
Assay: External sensory organ morphology and viability
Method: Visual inspection
Scope: Genome-wide
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Tissue
Biomodel: pnr-GAL4
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: Phenotype strength
Cutoff: np
Notes:

Serratia marcescens infection (1)
CG8447
CG8447
-1.8 Decreased viability after Serratia marcescens infection no

Reference

Genome-wide RNAi screen identifies genes involved in intestinal pathogenic bacterial infection. Cronin et al., 2009

Innate immunity represents the first line of defense in animals. We report a genome-wide in vivo Drosophila RNA interference screen to uncover genes involved in susceptibility or resistance to intestinal infection with the bacterium Serratia marcescens. We first employed whole-organism gene suppression, followed by tissue-specific silencing in gut epithelium or hemocytes to identify several hundred genes involved in intestinal antibacterial immunity. Among the pathways identified, we showed that the JAK-STAT signaling pathway controls host defense in the gut by regulating stem cell proliferation and thus epithelial cell homeostasis. Therefore, we revealed multiple genes involved in antibacterial defense and the regulation of innate immunity.

Screen details

Stable Id: GR00142-A-1
Screen title: Serratia marcescens infection (1)
Assay: Heat shock and viability
Method: Fly count
Scope: Random genes
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Organism
Biomodel: HSP70-GAL4; TubGAL80ts
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: Days life time (LT50)
Cutoff: < -1.5 SD OR > 2 SD
Notes:

Muscle morphogenesis and function (1)
CG33964
CG33964
np none no

Reference

Systematic genetic analysis of muscle morphogenesis and function in Drosophila. Schnorrer et al., 2010

Systematic genetic approaches have provided deep insight into the molecular and cellular mechanisms that operate in simple unicellular organisms. For multicellular organisms, however, the pleiotropy of gene function has largely restricted such approaches to the study of early embryogenesis. With the availability of genome-wide transgenic RNA interference (RNAi) libraries in Drosophila, it is now possible to perform a systematic genetic dissection of any cell or tissue type at any stage of the lifespan. Here we apply these methods to define the genetic basis for formation and function of the Drosophila muscle. We identify a role in muscle for 2,785 genes, many of which we assign to specific functions in the organization of muscles, myofibrils or sarcomeres. Many of these genes are phylogenetically conserved, including genes implicated in mammalian sarcomere organization and human muscle diseases.

Screen details

Stable Id: GR00134-A-1
Screen title: Muscle morphogenesis and function (1)
Assay: Posture, locomotion, flight and viability
Method: Visual inspection
Scope: Genome-wide
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Tissue
Biomodel: Mef2-GAL4
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: rp
Cutoff: S19 > 0.5
Notes:

Heart development and function (1)
CG33964|CG13175
1 none no

Reference

A global in vivo Drosophila RNAi screen identifies NOT3 as a conserved regulator of heart function. Neely et al., 2010

Heart diseases are the most common causes of morbidity and death in humans. Using cardiac-specific RNAi-silencing in Drosophila, we knocked down 7061 evolutionarily conserved genes under conditions of stress. We present a first global roadmap of pathways potentially playing conserved roles in the cardiovascular system. One critical pathway identified was the CCR4-Not complex implicated in transcriptional and posttranscriptional regulatory mechanisms. Silencing of CCR4-Not components in adult Drosophila resulted in myofibrillar disarray and dilated cardiomyopathy. Heterozygous not3 knockout mice showed spontaneous impairment of cardiac contractility and increased susceptibility to heart failure. These heart defects were reversed via inhibition of HDACs, suggesting a mechanistic link to epigenetic chromatin remodeling. In humans, we show that a common NOT3 SNP correlates with altered cardiac QT intervals, a known cause of potentially lethal ventricular tachyarrhythmias. Thus, our functional genome-wide screen in Drosophila can identify candidates that directly translate into conserved mammalian genes involved in heart function.

Screen details

Stable Id: GR00138-A-1
Screen title: Heart development and function (1)
Assay: Viability
Method: Fly count
Scope: Selected genes
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Tissue
Biomodel: TinCΔ4 12a-Gal4
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: Developmental lethality
Cutoff: <= 0.6666
Notes:

Adiposity regulation (1)
CG8447
-0.23 none no

Reference

Drosophila genome-wide obesity screen reveals hedgehog as a determinant of brown versus white adipose cell fate. Pospisilik et al., 2010

Over 1 billion people are estimated to be overweight, placing them at risk for diabetes, cardiovascular disease, and cancer. We performed a systems-level genetic dissection of adiposity regulation using genome-wide RNAi screening in adult Drosophila. As a follow-up, the resulting approximately 500 candidate obesity genes were functionally classified using muscle-, oenocyte-, fat-body-, and neuronal-specific knockdown in vivo and revealed hedgehog signaling as the top-scoring fat-body-specific pathway. To extrapolate these findings into mammals, we generated fat-specific hedgehog-activation mutant mice. Intriguingly, these mice displayed near total loss of white, but not brown, fat compartments. Mechanistically, activation of hedgehog signaling irreversibly blocked differentiation of white adipocytes through direct, coordinate modulation of early adipogenic factors. These findings identify a role for hedgehog signaling in white/brown adipocyte determination and link in vivo RNAi-based scanning of the Drosophila genome to regulation of adipocyte cell fate in mammals.

Screen details

Stable Id: GR00190-A-1
Screen title: Adiposity regulation (1)
Assay: Total fly triglyceride expression
Method: Colorimetric determination
Scope: Genome-wide
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Organism
Biomodel: Hsp70-GAL4;Tub-GAL80ts
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: Triglyceride change
Cutoff: Z-score > 1.65 after 3 screening rounds
Notes: Additional information about the primary screen

Heat nociception (1)
CG8447
CG13175
0 Developmentally lethal yes

Reference

A genome-wide Drosophila screen for heat nociception identifies α2δ3 as an evolutionarily conserved pain gene. Neely et al., 2010

Worldwide, acute, and chronic pain affects 20% of the adult population and represents an enormous financial and emotional burden. Using genome-wide neuronal-specific RNAi knockdown in Drosophila, we report a global screen for an innate behavior and identify hundreds of genes implicated in heat nociception, including the α2δ family calcium channel subunit straightjacket (stj). Mice mutant for the stj ortholog CACNA2D3 (α2δ3) also exhibit impaired behavioral heat pain sensitivity. In addition, in humans, α2δ3 SNP variants associate with reduced sensitivity to acute noxious heat and chronic back pain. Functional imaging in α2δ3 mutant mice revealed impaired transmission of thermal pain-evoked signals from the thalamus to higher-order pain centers. Intriguingly, in α2δ3 mutant mice, thermal pain and tactile stimulation triggered strong cross-activation, or synesthesia, of brain regions involved in vision, olfaction, and hearing.

Screen details

Stable Id: GR00135-A-1
Screen title: Heat nociception (1)
Assay: Noxious heat avoidance and viability
Method: Fly count
Scope: Genome-wide
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Organism
Biomodel: elav-GAL4
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: Z-score
Cutoff: > 1.65
Notes: Additional information about secondary screens (geotactic, phototaxis, and temperature sensitivity)

Heat nociception (1)
CG8447
CG33964
0 Developmentally lethal yes

Reference

A genome-wide Drosophila screen for heat nociception identifies α2δ3 as an evolutionarily conserved pain gene. Neely et al., 2010

Worldwide, acute, and chronic pain affects 20% of the adult population and represents an enormous financial and emotional burden. Using genome-wide neuronal-specific RNAi knockdown in Drosophila, we report a global screen for an innate behavior and identify hundreds of genes implicated in heat nociception, including the α2δ family calcium channel subunit straightjacket (stj). Mice mutant for the stj ortholog CACNA2D3 (α2δ3) also exhibit impaired behavioral heat pain sensitivity. In addition, in humans, α2δ3 SNP variants associate with reduced sensitivity to acute noxious heat and chronic back pain. Functional imaging in α2δ3 mutant mice revealed impaired transmission of thermal pain-evoked signals from the thalamus to higher-order pain centers. Intriguingly, in α2δ3 mutant mice, thermal pain and tactile stimulation triggered strong cross-activation, or synesthesia, of brain regions involved in vision, olfaction, and hearing.

Screen details

Stable Id: GR00135-A-1
Screen title: Heat nociception (1)
Assay: Noxious heat avoidance and viability
Method: Fly count
Scope: Genome-wide
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Organism
Biomodel: elav-GAL4
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: Z-score
Cutoff: > 1.65
Notes: Additional information about secondary screens (geotactic, phototaxis, and temperature sensitivity)

Muscle morphogenesis and function (1)
CG33964
CG33964
np none no

Reference

Systematic genetic analysis of muscle morphogenesis and function in Drosophila. Schnorrer et al., 2010

Systematic genetic approaches have provided deep insight into the molecular and cellular mechanisms that operate in simple unicellular organisms. For multicellular organisms, however, the pleiotropy of gene function has largely restricted such approaches to the study of early embryogenesis. With the availability of genome-wide transgenic RNA interference (RNAi) libraries in Drosophila, it is now possible to perform a systematic genetic dissection of any cell or tissue type at any stage of the lifespan. Here we apply these methods to define the genetic basis for formation and function of the Drosophila muscle. We identify a role in muscle for 2,785 genes, many of which we assign to specific functions in the organization of muscles, myofibrils or sarcomeres. Many of these genes are phylogenetically conserved, including genes implicated in mammalian sarcomere organization and human muscle diseases.

Screen details

Stable Id: GR00134-A-1
Screen title: Muscle morphogenesis and function (1)
Assay: Posture, locomotion, flight and viability
Method: Visual inspection
Scope: Genome-wide
Screen type: in vivo
Species: Drosophila melanogaster
Biosource: Tissue
Biomodel: Mef2-GAL4
Library: VDRC, np
Reagent type: UAS-IR construct
Score type: rp
Cutoff: S19 > 0.5
Notes:

Reagent information for gene 3772719 (CG33964)

Reagent IDTypeLibrary
HFA07184 dsRNA
Heidelberg Fly Array (HFA)|Boutros Lab|1|FlyBase release 2|21306|dsRNA|http://b110-wiki.dkfz.de/signaling/wiki/display/rnaiwiki/Drosophila+RNAi+libraries
HFA06301 dsRNA
Heidelberg Fly Array (HFA)|Boutros Lab|1|FlyBase release 2|21306|dsRNA|http://b110-wiki.dkfz.de/signaling/wiki/display/rnaiwiki/Drosophila+RNAi+libraries
MRC100_G05 dsRNA
MRC|MRC|1|FlyBase release 2|13089|dsRNA|http://www.hutchison-mrc.cam.ac.uk/
BKN40103 dsRNA
BKN|Boutros Lab|1|FlyBase release 4, 5|19708|dsRNA|http://b110-wiki.dkfz.de/signaling/wiki/display/rnaiwiki/Drosophila+RNAi+libraries
AMB21345 dsRNA
Ambion|Ambion|1|FlyBase release 2|13071|dsRNA|http://www.invitrogen.com/site/us/en/home/brands/ambion.html?CID=fl-ambion
DRSC06301 dsRNA
DRSC|Drosophila RNAi Screening Center (DRSC)|2|FlyBase release 2 - 5|42076|dsRNA|http://www.flyrnai.org/
MRC086_B05 dsRNA
MRC|MRC|1|FlyBase release 2|13089|dsRNA|http://www.hutchison-mrc.cam.ac.uk/
DRSC07184 dsRNA
DRSC|Drosophila RNAi Screening Center (DRSC)|2|FlyBase release 2 - 5|42076|dsRNA|http://www.flyrnai.org/
MRC135_A01 dsRNA
MRC|MRC|1|FlyBase release 2|13089|dsRNA|http://www.hutchison-mrc.cam.ac.uk/
MRC135_B01 dsRNA
MRC|MRC|1|FlyBase release 2|13089|dsRNA|http://www.hutchison-mrc.cam.ac.uk/
HFA06300 dsRNA
Heidelberg Fly Array (HFA)|Boutros Lab|1|FlyBase release 2|21306|dsRNA|http://b110-wiki.dkfz.de/signaling/wiki/display/rnaiwiki/Drosophila+RNAi+libraries
DRSC06300 dsRNA
DRSC|Drosophila RNAi Screening Center (DRSC)|2|FlyBase release 2 - 5|42076|dsRNA|http://www.flyrnai.org/
BKN40125 dsRNA
BKN|Boutros Lab|1|FlyBase release 4, 5|19708|dsRNA|http://b110-wiki.dkfz.de/signaling/wiki/display/rnaiwiki/Drosophila+RNAi+libraries
DRSC36182 dsRNA
DRSC|Drosophila RNAi Screening Center (DRSC)|2|FlyBase release 2 - 5|42076|dsRNA|http://www.flyrnai.org/
50775 UAS-IR construct
GD|Vienna Drosophila RNAi Center (VDRC)|1|FlyBase release 3|21066|UAS-IR construct|http://stockcenter.vdrc.at/control/main
50776 UAS-IR construct
GD|Vienna Drosophila RNAi Center (VDRC)|1|FlyBase release 3|21066|UAS-IR construct|http://stockcenter.vdrc.at/control/main
50719 UAS-IR construct
GD|Vienna Drosophila RNAi Center (VDRC)|1|FlyBase release 3|21066|UAS-IR construct|http://stockcenter.vdrc.at/control/main
50720 UAS-IR construct
GD|Vienna Drosophila RNAi Center (VDRC)|1|FlyBase release 3|21066|UAS-IR construct|http://stockcenter.vdrc.at/control/main
24099 UAS-IR construct
GD|Vienna Drosophila RNAi Center (VDRC)|1|FlyBase release 3|21066|UAS-IR construct|http://stockcenter.vdrc.at/control/main
24100 UAS-IR construct
GD|Vienna Drosophila RNAi Center (VDRC)|1|FlyBase release 3|21066|UAS-IR construct|http://stockcenter.vdrc.at/control/main

Gene information for gene 3772719 (CG33964)

Gene:
Alternate gene names:CG8447, CT32415, CG13174, DmelCG33964, CG33154
Description:
Chromosome:2R
Locus:
Biotype:protein-coding
Status:live
Entrez Gene ID:
Homologs:1
FLYBASE:
Uniprot:
RefSeq ID: -

Homologs:

GeneChromosomeLocusOrganism
C12orf261212q21.31Homo sapiens

GBrowse information for gene 3772719 (CG33964)