NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE155332 Query DataSets for GSE155332
Status Public on Sep 24, 2020
Title Aging of preleukemic thymocytes drives CpG island hypermethylation in T-cell acute lymphoblastic leukemia [ChIPmentation_TALL]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Cancer cells display DNA hypermethylation at specific CpG islands in comparison to their normal healthy counterparts, but the mechanism that drives this so-called CpG island methylator phenotype (CIMP) remains poorly understood. Here, we show that CpG island methylation in human T-cell acute lymphoblastic leukemia (T-ALL) mainly occurs at promoters of PRC2 target genes that are not expressed in normal or malignant T-cells and which display a reciprocal association with H3K27me3 binding. In addition, we found that this aberrant methylation profile shows a strong correlation with the epigenetic age of the leukemic T cells and elucidate that a similar CpG island methylation signature is gradually established in aging pre-leukemic thymocytes from CD2-Lmo2 transgenic mice. Finally, we unexpectedly uncover that this age-related CpG island hypermethylation signature is completely resistant to the FDA-approved hypomethylating agent Decitabine. Altogether, our work demonstrates that DNA methylation reflects the epigenetic history of leukemic T cells and suggests that methylation-based subtypes of human T-ALL have followed a different trajectory towards T-cell transformation, possibly mediated by differences in the self-renewing capacity of the putative T-ALL cell-of-origin. Given that the concept of preleukemic thymocytes has only been reported in T-ALL mouse models so far, we here provide, for the first time, conceptual evidence that a pre-leukemic phase might also be involved in the pathogenesis of the human disease.
 
Overall design ChIPmentation for histone marks on 6 T-ALL samples with input controls
 
Contributor(s) Roels J, Thénoz M, Van Vlierberghe P
Citation(s) 33458694
Submission date Jul 29, 2020
Last update date Mar 18, 2021
Contact name Juliette Roels
E-mail(s) roels.juliette@gene.com
Phone 6505807476
Organization name Genentech
Street address 1 DNA Way
City South San Francisco
State/province CA
ZIP/Postal code 94080
Country USA
 
Platforms (1)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
Samples (18)
GSM4699227 H3K27me3 T_ALL1 ChIPmentation
GSM4699228 H3K27me3 T_ALL2 ChIPmentation
GSM4699229 H3K27me3 T_ALL3 ChIPmentation
This SubSeries is part of SuperSeries:
GSE155339 Aging of preleukemic thymocytes drives CpG island hypermethylation in T-cell acute lymphoblastic leukemia
Relations
BioProject PRJNA649428
SRA SRP274090

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE155332_H3K27ac_normalized_counts.txt.gz 5.8 Mb (ftp)(http) TXT
GSE155332_H3K27ac_raw_counts.txt.gz 4.7 Mb (ftp)(http) TXT
GSE155332_H3K27me3_TALL_normalized_counts.txt.gz 4.5 Mb (ftp)(http) TXT
GSE155332_H3K27me3_TALL_raw_counts.txt.gz 3.2 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap