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Sample GSM4981943 Query DataSets for GSM4981943
Status Public on Dec 21, 2020
Title Terminal tracheal cells _ Pe2_Dam_rep2
Sample type SRA
 
Source name Dam-control processed DNA from adult terminal tracheal cells expressing LT3-Dam in damaged intestine (Pe)
Organism Drosophila melanogaster
Characteristics genotype: w-; dSRF-GAL4, UAS-CD8GFP/+; tub-GAL80ts/UAS-LT3-Dam
treatment: treated with bacteria solution (Pe) for 16hrs
tissue: tracheal cells
Treatment protocol During the last 16 hrs at 29°C, flies were fed a Sucrose or Sucrose + Pe solution.
Growth protocol Animals were crossed at 18°C. F1 progeny were collected every 48 hrs and aged for a further 7 days at 18°C before transferring to 29°C to induce adult restricted Dam protein expression for 24 hrs.
Extracted molecule genomic DNA
Extraction protocol 60 midguts with associated TTCs per condition per biological replicate were dissected in cold PBS and stored at -80°C. Genomic DNA was isolated, RNAseA treated and DpnI digested. DamID adaptors were ligated to DpnI digested DNA followed by DpnII digestion PCR amplification, sonication and removal of DamID adaptors (Marshall et al., 2016).
Libraries were generated using the NEBNext® Ultra™ II DNA Library Prep Kit for Illumina.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina NextSeq 500
 
Description Pe2.gff
Data processing Library strategy: DamID-seq
Sequencing data from TaDa experiments were processed using a previously described pipeline (Marshall et al., 2015)
Reads were mapped to release 6.11 of the Drosophila genome.
Transcribed genes were annotated from Pol II binding data using a custom Perl script (available at https://github.com/tonysouthall/Dam-RNA_POLII_analysis).
Ratio files (log2) were then generated from the experimental and Dam-only control data.
Transcribed genes were identified based on meeting a threshold of 1% FDR and > 0.2 log2 ratios.
Genome_build: BDGP6
Supplementary_files_format_and_content: log2 normalised fold changes between the experimental and Dam-only control as a gff file produced by the damidseq_pipeline
 
Submission date Dec 20, 2020
Last update date Dec 22, 2020
Contact name Tony David Southall
E-mail(s) [email protected]
Organization name Imperial College London
Department Life Sciences
Lab Southall lab
Street address South Kensington Campus
City London
ZIP/Postal code SW7 2AZ
Country United Kingdom
 
Platform ID GPL19132
Series (1)
GSE163570 Profiling of RNA Pol II occupancy in adult Drosophila terminal tracheal cell using TaDa (Targeted DamID) in context of homeostasis or damaged intestine
Relations
BioSample SAMN17124839
SRA SRX9708003

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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