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SRX1837296: GSM2197447: H3K9me3 white-embKD_3; Drosophila melanogaster; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 43.2M spots, 2.2G bases, 1,001.2Mb downloads

Submitted by: NCBI (GEO)
Study: Piwi is required during Drosophila embryogenesis to license dual-strand piRNA clusters for transposon repression in adult ovaries [ChIP-seq]
show Abstracthide Abstract
Most piRNAs in the Drosophila female germline are transcribed from heterochromatic regions called dual-strand piRNA clusters. Histone 3 lysine 9 trimethylation (H3K9me3) is required for licensing piRNA production by these clusters. However, it is unclear when and how they acquire this permissive heterochromatic state. Although it has been suggested that piRNA cluster licensing is Piwi-independent, here we show that transient Piwi depletion in Drosophila embryos, using a refined knock-down system, results in H3K9me3 decrease at piRNA clusters. This is accompanied by aberrant maturation of piRNA precursor transcripts, accumulation of transposable element transcripts and female sterility. Conversely, Piwi knock-down at later developmental stages does not disturb piRNA cluster licensing, as previously reported. These results indicate that the identity of piRNA clusters is epigenetically acquired in a Piwi-dependent manner during a limited embryonic development window, which is reminiscent of the widespread genome reprogramming occurring during early mammalian zygotic development. Overall design: 3 independate biological triplicates of Chip H3K9me3 input and IP were performed for each of the 2 genotypes (piwi-embKD and white_embKD).
Sample: H3K9me3 white-embKD_3
SAMN05226683 • SRS1496691 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500.
Experiment attributes:
GEO Accession: GSM2197447
Links:
Runs: 1 run, 43.2M spots, 2.2G bases, 1,001.2Mb
Run# of Spots# of BasesSizePublished
SRR365765243,174,1432.2G1,001.2Mb2017-04-28

ID:
2622184

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