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Status |
Public on Aug 01, 2013 |
Title |
Expression profile and RNA Polymerase II occupancy of transposable elements among knock down of the piRNA pathway components in OSCs |
Organism |
Drosophila melanogaster |
Experiment type |
Expression profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing
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Summary |
The Piwi–piRNA complex (Piwi–piRISC) in Drosophila ovarian somatic cells represses transposons transcriptionally to maintain genome integrity; however, the underlying mechanisms remain obscure. We performed mRNA-seq analysis from OSCs transfected with siRNAs against CG3893, the known piRNA pathway genes, Piwi, Maelstrom, HP1a and Armitage, and the control (EGFP), and PolII ChIP-seqanalysis from OSCs transfected with siRNAs against CG3893, Piwi, Mael and the control (EGFP). This result indicates that CG3893 is a novel factor for primary piRNA pathway in OSCs.
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Overall design |
RNA levels in wild-type (EGFP control knock-down) ovarian somatic cells (OSC) and RNAi knock-downs of Piwi, Armi, Mael, CG3893, and HP1a. RNA Polymerase II occupancy in wild-type (EGFP control knock-down) ovarian somatic cells (OSC) and RNAi knock-downs of Piwi, Mael, and CG3893.
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Contributor(s) |
Ohtani H, Saito K, Siomi H |
Citation(s) |
23913921 |
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Submission date |
May 16, 2013 |
Last update date |
Jul 03, 2021 |
Contact name |
Yuka W. Iwasaki |
E-mail(s) |
iwasaki@keio.jp
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Organization name |
Keio University School of Medicine
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Department |
Department of Molecular Biology
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Lab |
Siomi Lab
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Street address |
35 Shinanomachi, Shinjuku-ku,
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City |
Tokyo |
ZIP/Postal code |
160-8582 |
Country |
Japan |
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Platforms (2) |
GPL13304 |
Illumina HiSeq 2000 (Drosophila melanogaster) |
GPL16479 |
Illumina MiSeq (Drosophila melanogaster) |
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Samples (10)
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Relations |
BioProject |
PRJNA203266 |
SRA |
SRP022848 |