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SRX19799391: GSM7120255: D1221C18_ChIP_p50_D2-24h_Bmori-v4_H3K4me3_rep2_IP; Bombyx mori; ChIP-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 24.5M spots, 4.9G bases, 1.6Gb downloads

External Id: GSM7120255_r1
Submitted by: UMR3664, Institut Curie
Study: Unique territorial and sub-chromosomal organization revealed in the holocentric moth Bombyx mori [ChIP-seq]
show Abstracthide Abstract
Genome organization in diverse eukaryotes follows conserved principles including the formation of chromosome territories (CT), chromatin compartments, and TADs. Here, we describe the 3D architecture of holocentric chromosomes in the silkworm Bombyx mori. At the genome-wide scale, B. mori chromosomes are highly territorial lacking any visible trans contact pattern. At the chromosomal scale, B. mori chromosomes segregate into three chromatin compartments: an active A and an inactive B as described in other eukaryotes, and a third type, X, with a unique contact pattern. Compartment X is strongly enriched for short-range interactions and depleted of long-range interactions, hosts a specific combination of genetic and epigenetic features and localizes towards the periphery of CT. Biophysical simulations reveal the necessity of the combined effects of affinity-based compartmentalization and activity-based loop extrusion to lead to the unique interaction patterns observed. Our analyses contribute to our understanding how chromosomes fold highlighting the evolutionary plasticity of 3D genome organization. Overall design: Hi-C and ChIP-seq and RNA-seq data from Bombyx mori p50 reference strain embryos post-diapause. ChIP-seq experimments are all performed in duplicates. Hi-C have been done at several embryonic time points: 2h, 24h and 48h after dipause release and on adults heads. RNA-seq has been perfomred at 24h after diapause release
Sample: D1221C18_ChIP_p50_D2-24h_Bmori-v4_H3K4me3_rep2_IP
SAMN33955674 • SRS17161682 • All experiments • All runs
Organism: Bombyx mori
Library:
Name: GSM7120255
Instrument: Illumina NovaSeq 6000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: PAIRED
Construction protocol: Eggs were placed in 1% formaldehyde before chorions were broken with a piston pellet to allow embryos fixation for 10 min. After quenching and cell lysis, embyo tissus were ruptured and chromatin was sonicated using a E220 focused-ultrasonicator (Covaris). ChIP-seq libraries were prepared using the KAPA HyperPrep Library Preparation Kit complemented with Illumina TruSeq DNA UD Indexes. Libraries were amplified using 8-14 cycles on the thermocycler. Post amplification libraries were size selected at 250-600bp in length using SPRIselect beads from Beckman Coulter. Libraries were validated using the Agilent High Sensitivity screenTapes.
Runs: 1 run, 24.5M spots, 4.9G bases, 1.6Gb
Run# of Spots# of BasesSizePublished
SRR2399586924,527,0784.9G1.6Gb2023-09-17

ID:
27144094

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