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Status |
Public on Mar 28, 2014 |
Title |
GATA1s induces hyperproliferation of eosinophil precursors in Down syndrome transient leukemia |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Transient leukemia (TL) is evident in 5-10% of all neonates with Down syndrome (DS) and associated with N-terminal truncating GATA1-mutations (GATA1s). Here we analyzed the effect of on gene expression upon ectopic expression of Gata1s or Gata1, while simultaneously knocking down endogenous GATA1, in wild-type CD34+-hematopoietic stem and progenitor cells during myeloid differentiation. Ectopic expression of Gata1s, but not Gata1, in wild-type CD34+-hematopoietic stem and progenitor cells induced hyperproliferation of eosinophil promyelocytes in vitro. While GATA1s retained the function of GATA1 to induce eosinophil genes by occupying their promoter regions, GATA1s was impaired in its ability to repress oncogenic MYC and the pro-proliferative E2F transcription network.
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Overall design |
We lentivirally transduced wild-type CD34+-hematopoietic stem and progenitor cells to ectopically express Gata1s or Gata1, while simultaneously knocking down endogenous GATA1, and cultured them in myeloid differentiation for 0, 4 and 14 days.
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Contributor(s) |
Maroz A, Klusmann J |
Citation(s) |
24336126 |
Submission date |
Mar 28, 2014 |
Last update date |
Jan 23, 2019 |
Contact name |
Jan-Henning Klusmann |
E-mail(s) |
jan-henning.klusmann@kgu.de
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Organization name |
Goehte University Frankfurt
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Department |
Pediatric Hematology and Oncology
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Street address |
Theodor-Stern-Kai 7
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City |
Frankfurt |
ZIP/Postal code |
60590 |
Country |
Germany |
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Platforms (1) |
GPL6480 |
Agilent-014850 Whole Human Genome Microarray 4x44K G4112F (Probe Name version) |
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Samples (9)
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Relations |
BioProject |
PRJNA242933 |