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SRX13811043: GSM5821064: WGBS_TALL-1; Homo sapiens; Bisulfite-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 738.1M spots, 222.9G bases, 72.3Gb downloads

Submitted by: NCBI (GEO)
Study: Acute lymphoblastic leukemia displays a distinct highly methylated genome
show Abstracthide Abstract
DNA methylation is tightly regulated during development and is stably maintained in normal cells. In contrast, the methylome of cancer cells is commonly characterized by a global loss of DNA methylation co-occurring with CpG island hypermethylation. In acute lymphoblastic leukemia (ALL), the commonest childhood cancer, perturbations of CpG methylation have been reported to be associated with genetic disease subtype and outcome, but data examining large cohorts at genome-wide scale are lacking. Here, we performed whole-genome bisulfite sequencing of leukemic cells across multiple subtypes of ALL, leukemia cell lines and normal hematopoietic cells, and show that in contrast to most cancers, ALL samples only exhibit CpG island hypermethylation but minimal global loss of methylation. This was most pronounced in T-ALL and accompanied by an exceptionally broad range of hypermethylation of CpG islands between patients that is influenced by TET2 and DNMT3B. These findings demonstrate that ALL is characterized by an unusually highly methylated genome, and provide insights into the deregulation of methylation in cancer. Overall design: Genome-wide DNA methylation profiling of B-ALL and T-ALL cell lines as well as DNA methylation and expression profiling of Jurkat cells with TET2 knockout.
Sample: WGBS_TALL-1
SAMN25042766 • SRS11691762 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2000
Strategy: Bisulfite-Seq
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Cells at exponential growth phase were spun down at 1500 rpm for 3 minutes and cell pellet was used to extract genomic DNA. Whole genome bisulfite sequencing was performed on bisulfite-modified DNA-sequencing library generated according to Illumina's instructions accompanying the TruSeq DNA Methylation Kit (Part# EGMK81312). 200ng of genomic DNA, including 0.2% Lambda DNA (N6-methyladenine-free; NEB) was bisulfite converted in a single reaction using the EZ DNA Methylation Gold Kit (Zymo Research) as outlined by the manufacturer. The bisulfite converted DNA (bsDNA) was split into four aliquots per sample. Four single indexed WGBS libraries were constructed with the EpiGnome Methyl-Seq kit (EGMK81312, Epicentre) according to the manufacturer's recommendations. The final concentration of each library was accurately determined through qPCR (KAPA Biosystems). The four independent libraries were normalized, pooled, and loaded across three lanes of the HiSeq 2000 instrument (Illumina).
Experiment attributes:
GEO Accession: GSM5821064
Links:
Runs: 1 run, 738.1M spots, 222.9G bases, 72.3Gb
Run# of Spots# of BasesSizePublished
SRR17642783738,053,980222.9G72.3Gb2022-03-03

ID:
19231540

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