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SRX9695112: GSM4978089: D0_shCTCF_rep1 [BL-Hi-C]; Mus musculus; Hi-C
1 ILLUMINA (Illumina NovaSeq 6000) run: 62.9M spots, 18.9G bases, 5.7Gb downloads

Submitted by: NCBI (GEO)
Study: CTCF Functions as an Insulator for Somatic Genes and a Structural Regulator for Pluripotent Genes during Reprogramming [BL-Hi-C]
show Abstracthide Abstract
CCCTC binding factor (CTCF) has been implicated in mediating chromatin insulation and long-distance interactions between enhancer and promoter. In this study, to study the roles of CTCF in somatic cell reprogramming, we performed RNA-seq, Hi-C, ChIP-seq and ATAC-seq at the specific stage of reprogramming. Through bioinformatics analysis, our data indicated that CTCF promotes enhancer-promoter interactions and chromatin accessibility to regulate the expression of key pluripotency genes; meanwhile, it serves as an insulator to suppress the expression of key somatic genes. Smarca5 loss inhibits CTCF-promoted reprogramming by reversing CTCF insulator activity on MEF-specific genes and leading to incorrect nucleosome positioning adjacent to CTCF binding sites. These findings reveal the dual functions of CTCF as both a structural regulator and insulator in conjunction with a key chromatin remodeler to drive cellular reprogramming towards pluripotency. Overall design: Examination of chromatin interactions in mouse embryonic fibroblast (MEF) and OSKM reprogrammed cells on day 10. Examination of chromatin interactions in reprogramming cells with OSKM plus control, OSKM plus Ctcf overexpression and OSKM with Ctcf overexpression plus Smarca5 knockdown, reprogramming cells with OSKM plus control or Ctcf shRNA on day 10. Examination of chromatin interactions in sorted reprogramming intermediate cells in the TetOn lentivirus OSKM reprogramming system with both control shRNA and Ctcf knockdown by BL-Hi-C deep sequencing.
Sample: D0_shCTCF_rep1 [BL-Hi-C]
SAMN17099218 • SRS7891710 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina NovaSeq 6000
Strategy: Hi-C
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: The BL-Hi-C libraries were performed as previous described. Briefly, the cells were treated with 1% formaldehyde for 10 min at RT and the crosslink was quenched by adding 2.5 M glycine. Then, the cells were treated with 0.1% SDS FA lysis buffer and 1% SDS FA lysis buffer. After that, the genome was digested with enzyme HaeIII into fragments with blunt-ends, which were treated with adenine and ligated with bridge linker containing biotin for 4 hr at 16°C. The unligated DNA fragments were digested with DNA exonuclease. Next, the cells were treated with SDS and proteinase K to digest proteins, and the DNA was purified using phenol-chloroform extraction with ethanol precipitation. Then, the DNA was fragmented into 300 bp on average by sonication and the biotin-labeled DNA fragments were pulled down with streptavidin coated M280 beads. The BL-Hi-C libraries were constructed into standard Illumina libraries.
Experiment attributes:
GEO Accession: GSM4978089
Links:
Runs: 1 run, 62.9M spots, 18.9G bases, 5.7Gb
Run# of Spots# of BasesSizePublished
SRR1326473462,862,33618.9G5.7Gb2022-04-06

ID:
12680918

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