 |
 |
GEO help: Mouse over screen elements for information. |
|
| Status |
Public on Feb 12, 2024 |
| Title |
Non-canonical functions of UHRF1 maintain DNA methylation homeostasis in cancer cells |
| Organism |
Homo sapiens |
| Experiment type |
Methylation profiling by high throughput sequencing
|
| Summary |
DNA methylation is an essential epigenetic mark in mammals. It controls gene expression and genome stability. Global DNA methylation pattern is abnormal in cancers. Ubiquitin like with PHD and RING finger domains 1 (UHRF1) is a key epigenetic regulator that recruits and activates DNA methyltransferase 1 (DNMT1), the methylation maintenance enzyme. UHRF1 is a proven oncogene and its overexpression transforms cells in vitro and causes cancer in animal models. Therefore, UHRF1 provides a unique entry point into the links between epigenetics and cancer. However, it is still not fully clear how UHRF1 works in cancer cells. To understand UHRF1 functions in cancer, we employed experimental strategy to use an advanced chemical/genetic system, the auxin-inducible degron (AID) technology, whereby the degron-fused protein can be totally and rapidly degraded upon the addition of a small molecule, auxin. We chose the human CRC cell line HCT116 as our model and successfully generated UHRF1-AID and DNMT1-AID. Through this study, we made the significant discovery that UHRF1 not only regulates DNMT1, but also influences the activities of de novo methyltransferases DNMT3A and DNMT3B, as well as the active demethylase TET2.
|
| |
|
| Overall design |
To elucidate the roles of UHRF1 and DNMT1 in the HCT116 cell line, we generated four distinct cell lines: wild-type (WT), UHRF1-AID, DNMT1-AID, and UHRF1-AID/DNMT1-AID. To analyze the kinetics of DNA methylation, we treated these cell lines with auxin for 0, 2, 4, 6, 8, and 12 days.
|
| |
|
| Contributor(s) |
YAMAGUCHI K, MIURA F, Bashtrykov P, KIRSH O, Jeltsch A, Ito T, Defossez P |
| Citation(s) |
38580649 |
| |
| Submission date |
Jun 28, 2023 |
| Last update date |
Apr 24, 2024 |
| Contact name |
Pierre-Antoine Defossez |
| E-mail(s) |
pierre-antoine.defossez@u-paris.fr
|
| Organization name |
Epigenetics and Cell Fate Unit
|
| Street address |
35 rue Hélène Brion
|
| City |
Paris |
| ZIP/Postal code |
75013 |
| Country |
France |
| |
|
| Platforms (1) |
|
| Samples (62)
|
|
| Relations |
| BioProject |
PRJNA988463 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE236026_Daid.Day0.cpg.methexport.tab.gz |
266.4 Mb |
(ftp)(http) |
TAB |
| GSE236026_Daid.Day12.cpg.methexport.tab.gz |
238.2 Mb |
(ftp)(http) |
TAB |
| GSE236026_Daid.Day2.cpg.methexport.tab.gz |
269.8 Mb |
(ftp)(http) |
TAB |
| GSE236026_Daid.Day4.cpg.methexport.tab.gz |
271.0 Mb |
(ftp)(http) |
TAB |
| GSE236026_Daid.Day6.cpg.methexport.tab.gz |
229.3 Mb |
(ftp)(http) |
TAB |
| GSE236026_Daid.Day8.cpg.methexport.tab.gz |
234.1 Mb |
(ftp)(http) |
TAB |
| GSE236026_RAW.tar |
483.8 Mb |
(http)(custom) |
TAR (of TAB) |
| GSE236026_UDaid.Day0.cpg.methexport.tab.gz |
270.2 Mb |
(ftp)(http) |
TAB |
| GSE236026_UDaid.Day12.cpg.methexport.tab.gz |
233.5 Mb |
(ftp)(http) |
TAB |
| GSE236026_UDaid.Day2.cpg.methexport.tab.gz |
267.1 Mb |
(ftp)(http) |
TAB |
| GSE236026_UDaid.Day4.cpg.methexport.tab.gz |
265.2 Mb |
(ftp)(http) |
TAB |
| GSE236026_UDaid.Day6.cpg.methexport.tab.gz |
227.9 Mb |
(ftp)(http) |
TAB |
| GSE236026_UDaid.Day8.cpg.methexport.tab.gz |
231.3 Mb |
(ftp)(http) |
TAB |
| GSE236026_Uaid.Day0.cpg.methexport.tab.gz |
265.7 Mb |
(ftp)(http) |
TAB |
| GSE236026_Uaid.Day12.cpg.methexport.tab.gz |
237.5 Mb |
(ftp)(http) |
TAB |
| GSE236026_Uaid.Day2.cpg.methexport.tab.gz |
268.3 Mb |
(ftp)(http) |
TAB |
| GSE236026_Uaid.Day4.cpg.methexport.tab.gz |
271.0 Mb |
(ftp)(http) |
TAB |
| GSE236026_Uaid.Day6.cpg.methexport.tab.gz |
227.8 Mb |
(ftp)(http) |
TAB |
| GSE236026_Uaid.Day8.cpg.methexport.tab.gz |
231.5 Mb |
(ftp)(http) |
TAB |
| GSE236026_WT.Day0.cpg.methexport.tab.gz |
223.0 Mb |
(ftp)(http) |
TAB |
| GSE236026_WT.Day12.cpg.methexport.tab.gz |
234.1 Mb |
(ftp)(http) |
TAB |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data are available on Series record |
|
|
|
|
 |
Less...
More...