Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Effect of expression of a PI3-Kinase Dp110 dominant-negative (Dp110-DN) trangene on gene expression in fly fat body

ABSTRACT: Gene expression pattern in fat bodies of flies expressing (or not) a dominant-negative form of the PI3K Dp110 (UAS-Dp110-DN, D954A) driven from a constitutive fat body-specific driver (FB-GAL4).

ORGANISM(S): Drosophila melanogaster

PROVIDER: GSE129430 | GEO | 2020/01/01

REPOSITORIES: GEO

ACCESS DATA

Json Xml

Similar Datasets

CLK targets from fly heads

Project description:CLK targets from fly heads using the TIM-GAL4; UAS-CLKGR line Keywords: CLK TARGETS

2007-07-09 | GSE7646 | GEO

Effect of reducing insulin signaling on third instar larval fat body gene expression in Drosophila melanogaster

Project description:We characterized insulin receptor (InR)-dependent gene expression in the Drosophila fat body using transgenic RNAi. Chronic knockdown of InR in the fat body was elicited via (r4-GAL4, UAS-InRi) and RNA-seq was used to identify potential target genes.

2017-10-24 | GSE97447 | GEO

Effect of expression of a PI3-Kinase Dp110 dominant-negative (Dp110-DN) trangene on gene expression in fly fat body

Project description:Effect of expression of a PI3-Kinase Dp110 dominant-negative (Dp110-DN) trangene on gene expression in fly fat body

| PRJNA531271 | ENA

3' RNA-seq of fly expressing cabut RNAi after exposure to different levels of sucrose

Project description:Control (+/cbtE1-UAS-cbt RNAi) or cabut RNAi flies (Tim-gal4, UAS-cbt RNAi) were starved for 16 hours and then exposed to food containing different concentrations of sucrose: 0, 25, 50 and 100 % for 18 hours. Fly heads were collected, RNA was extracted and RNA-seq libraries were prepared as previously described (Engreitz et al., 2013)

2015-05-08 | GSE58854 | GEO

Fly circadian clock, photoreceptors and fly hemolymph

Project description:Influence of diet and neuronal clk (clock) activity on hemolymph proteomics. We have shown that as photoreceptors die (in the fly) they necrose, which results in their intercellular contents leaking into the hemolymph. We hypothesize that this process is regulated by diet and circadian clock control. Analysis of differential protein expression in the hemolymph from flies reared on a high protein diet. Comparison of flies with and without a functional circadian clock within their photoreceptors. Species/Strain: Drosophila, Elav-GeneSwitch-GAL4>UAS-Clk-DN1 (+/- RU486), female

2021-01-30 | MSV000086781 | MassIVE

Transcription profiling of Drosophila fly heads treated with CHX, dexamethasone vs. controls

Project description:CLK targets from fly heads using the TIM-GAL4; UAS-CLKGR line Experiment Overall Design: Fly heads were stimulated with vehicle + CHX or dexamethasone + CHX

2008-06-15 | E-GEOD-7646 | biostudies-arrayexpress

Global quantitative proteomic analysis of aging Drosophila eyes

Project description:Wild-type Drosophila melanogaster expressing nuclear GFP-KASH fusion protein in photoreceptors for cell type-specific gene expression profiling (Rh1-Gal4>UAS-GFPKASH ; Genotype = w1118;; P{w+mC=[UAS-GFP-Msp300KASH}attP2, P{ry+t7.2=rh1-GAL4}3, ry506) were raised in 12:12h light:dark cycle at 25°C. Flies were aged for 10 or 40 days post-eclosion, and eyes were harvested from male flies for global quantitative proteomic analysis. Significantly changed proteins were identified that may contribute to age-associated retinal degeneration and loss of visual function in the aging Drosophila eye.

2021-07-23 | PXD027090 | Pride

Branching Gene Regulatory Network for Neurotransmitter versus Axonal Pathfinding

Project description:In previous studies we found that the two transcription factors collier (FB:knot, kn) [vertebrate Ebf1] and ladybird early (lbe) [vertebrate Lbx1/2], when co-misexpressed from elav-Gal4, generate ectopic Nplp1 neuropeptidergic cells in the entire ventral nerve cord during Dmel. embryonic development. We also found that the axon generated by the ectopic Nplp1 cells, seem to follow the same fascicle as the wild type Nplp1 neurons. Therefore we used RNA-seq on control and UAS‑col,lbe co-misexpression to find candidate factors important in axon pathfinding of the Nplp1 neurons. We also included single misexpression of UAS-col and UAS-lbe, together with co-misexpression of UAS-ap, eya, since we know that col and lbe activate those two factors during the cell fate specification of Nplp1 neurons.

2019-03-11 | GSE113260 | GEO

Expression from hemocytes misexpressing Idh-R195H vs. controls

Project description:Expression profile for hemocytes from hml-Gal4, UAS-2xEGFP larvae were compared to hemocytes from hml-Gal4, UAS-2xEGFP; UAS-Idh-R195H larvae

2014-10-03 | GSE62008 | GEO

Xrp1 governs the stress response program to spliceosome dysfunction

Project description:We investigated the changes in gene expression in response to reduced levels of Ecdysoneless (Ecd), and the role of Xrp1 in induction of transcriptional changes upon loss of Ecd in the developing wing disc of Drosophila. To do this we utilized the GAL4/UAS system to express UAS-ecd-RNAi alone and in combination with UAS-xrp1-RNAi in the nubbin-domain (nub-Gal4, UAS-mRFP, UAS-ecd-RNAi and nub-Gal4, UAS-mRFP, UAS-ecd-RNAi, xrp1-RNAi) of the wing disc and used nub-Gal4, UAS-mRFP wing discs as controls. We quantified transcriptomic expression analysis from four biological replicates for both experimental groups

2024-01-31 | GSE213298 | GEO

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data