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SRX17116755: GSM6472949: MARCM yki3SA sd 3; Drosophila melanogaster; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 19.3M spots, 1.8G bases, 595.6Mb downloads

External Id: GSM6472949_r1
Submitted by: Laboratory of Growth Control, VIB-KU Leuven Center for Cancer Biology, VIB-KU Leuven
Study: Hippo signaling instructs ectopic but not normal organ growth [Drosophila YkiHyper]
show Abstracthide Abstract
In order to study how ectopic Yki drives tissue overgrowth in Drosophila imaginal discs, we overexpressed the constitutively active Yki3SA and deleted wts in clones of cells in the entire eye-antennal imaginal disc, as well as specifically in eye disc proper cells using Optix-Gal4. Using the MARCM system allowed us to compare the effects of Yki3SA overexpression in wild-type and sd mutant clones. Overall design: Differential gene expression analysis of samples of eye-antennal imaginal discs with Yki hyperactivation and their corresponding controls: 1) eyFLP wts KO and eyFLP control; 2) optix>Yki3SA and optix control; 3) eyFLP MARCM Yki3SA and eyFLP MARCM ctrl as well as eyFLP MARCM Yki3SA sd- and eyFLP MARCM sd- to measure the effects of Yki hyperactivation in sd mutant clones.
Sample: MARCM yki3SA sd 3
SAMN30370806 • SRS14690904 • All experiments • All runs
Library:
Name: GSM6472949
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Drosophila imaginal discs were dissected and transferred into RNAse-free 1xPBS on ice; a minimum of 30 discs per sample were used. RNA was extracted immediately using the RNAeasy mini spin kit (Qiagen) and stored at -80°C. Library preparation was performed according to the QuantSeq 3' mRNA-Seq Library Prep kit FWD (Lexogen).
Runs: 1 run, 19.3M spots, 1.8G bases, 595.6Mb
Run# of Spots# of BasesSizePublished
SRR2110320919,286,9671.8G595.6Mb2022-11-18

ID:
23916026

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