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Status |
Public on Mar 31, 2011 |
Title |
Identification of Transcription Factor PES-1::GFP Binding Regions in L4 |
Project |
modENCODE
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Organism |
Caenorhabditis elegans |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
modENCODE_submission_3157 This submission comes from a modENCODE project of Michael Snyder. For full list of modENCODE projects, see http://www.genome.gov/26524648 Project Goal: We are identifying the DNA binding sites for 300 transcription factors in C. elegans. Each transcription factor gene is tagged with the same GFP fusion protein, permitting validation of the gene's correct spatio-temporal expression pattern in transgenic animals. Chromatin immunoprecipitation on each strain is peformed using an anti-GFP antibody, and any bound DNA is deep-sequenced using Solexa GA2 technology. For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODEDataReleasePolicyFinal2008.pdf
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Overall design |
EXPERIMENT TYPE: CHIP-seq. BIOLOGICAL SOURCE: Strain: OP87 (official name : OP87 genotype : unc-119(ed3) III; wgIs87 [unc-119(+) pes-1::TY1::EGFP::3xFLAG] outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston ); Developmental Stage: L4; Genotype: unc-119(ed3) III; wgIs87 [unc-119(+) pes-1::TY1::EGFP::3xFLAG]; Sex: Hermaphrodite; EXPERIMENTAL FACTORS: Developmental Stage L4; Target gene pes-1; Strain OP87 (official name : OP87 genotype : unc-119(ed3) III; wgIs87 [unc-119(+) pes-1::TY1::EGFP::3xFLAG] outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston ); temp (temperature) 20 degree celsius
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Web link |
http://www.modencode.org http://www.ncbi.nlm.nih.gov/geo/info/ENCODE.html
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Contributor(s) |
Zhong M, Snyder M, Slightam C, Kim S, Murray J, Waterston R, Gerstein M, Niu W, Janette J, Raha D, Agarwal A, Reinke V, Sarov M, Hyman A |
Citation(s) |
21177963 |
BioProject |
PRJNA63461 |
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Submission date |
Dec 17, 2010 |
Last update date |
May 15, 2019 |
Contact name |
DCC modENCODE |
E-mail(s) |
help@modencode.org
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Phone |
416-673-8579
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Organization name |
Ontario Institute for Cancer Research
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Lab |
modENCODE DCC
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Street address |
MaRS Centre, South Tower, 101 College Street, Suite 800
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City |
Toronto |
State/province |
Ontario |
ZIP/Postal code |
M5G 0A3 |
Country |
Canada |
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Platforms (1) |
GPL9309 |
Illumina Genome Analyzer (Caenorhabditis elegans) |
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Samples (9)
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GSM700168 |
Snyder_PES-1_GFP_L4_rep1 extraction1_seq1 aliquote 1 |
GSM700169 |
Snyder_PES-1_GFP_L4_rep1 extraction2_seq2 aliquote 1 |
GSM700170 |
Snyder_PES-1_GFP_L4_rep1 extraction3_seq3 aliquote 1 |
GSM700171 |
Snyder_PES-1_GFP_L4_rep1 extraction4_seq4 aliquote 1 |
GSM700172 |
Snyder_PES-1_GFP_L4_rep1 extraction5_seq5 aliquote 1 |
GSM700173 |
Snyder_PES-1_GFP_L4_rep1 extraction6_seq6 aliquote 1 |
GSM700174 |
Snyder_PES-1_GFP_L4_rep2 extraction7_seq7 aliquote 1 |
GSM700175 |
Snyder_PES-1_GFP_L4_rep2 extraction8_seq8 aliquote 1 |
GSM700176 |
Snyder_PES-1_GFP_L4_rep2 extraction9_seq9 aliquote 1 |
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Relations |
SRA |
SRP006200 |