Genome-wide mapping of Runx1-bound sites in early B-cell progenitors
Source: NCBI BioProject (ID PRJNA193697)
Source: NCBI BioProject (ID PRJNA193697)
0 0
Project name: Mus musculus
Description: The t(12;21) chromosomal translocation, targeting the gene encoding the RUNX1 transcription factor, is observed in 25% of pediatric acute lymphoblastic leukemia (ALL) and is an initiating event in the disease. To elucidate the mechanism by which RUNX1 disruption initiates leukemogenesis, we investigated its normal role in murine B-cell development. Gene expression analysis and genome-wide Runx1-occupancy studies support the hypothesis that Runx1 reinforces the transcription factor network in B-cell progenitors governing early B-cell survival and development .Overall design: ChIP-seq experiments were performed in the proB-cell line BMiFLT3(15-3), stably transduced with the transcription factor Runx1, to identify Runx1-bound sites in early B-cell progenitors.
Data type: Epigenomics
Sample scope: Multiisolate
Relevance: ModelOrganism
Organization: Molecular Pathology, Heinrich-Pette-Institute, Leibniz Institute for Experimental Virology
Literatures
- PMID: 23704093
Last updated: 2013-03-21