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  • keithforest
    Junior Member
    • Aug 2010
    • 7

    mouse bone marrow rna-seq data

    I'm new to the forum, so my apologies if there is a better place for this question.

    I am looking for rna-seq data from mouse bone marrow. Does anyone know if any is available, or where to look for it? I've tried GEO and couldn't find any relevant samples.

    Thanks in advance.
  • Joann
    Senior Member
    • Oct 2008
    • 230

    #2
    Expression profiling by array

    You are close. Recently posted here in the literature watch section:

    Bonadies N, Foster SD, Chan WI, Kvinlaug BT et al. Genome-wide analysis of transcriptional reprogramming in mouse models of acute myeloid leukaemia.
    PLoS One 2011 Jan 28;6(1):e16330. PMID: 21297973
    doi:10.1371/journal.pone.0016330

    Acute leukaemias are commonly caused by mutations that corrupt the transcriptional circuitry of haematopoietic stem/progenitor cells. However, the mechanisms underlying large-scale transcriptional reprogramming remain largely unknown. Here we investigated transcriptional reprogramming at genome-scale in mouse retroviral transplant models of acute myeloid leukaemia (AML) using both gene-expression profiling and ChIP-sequencing. We identified several thousand candidate regulatory regions with altered levels of histone acetylation that were characterised by differential distribution of consensus motifs for key haematopoietic transcription factors including Gata2, Gfi1 and Sfpi1/Pu.1. In particular, downregulation of Gata2 expression was mirrored by abundant GATA motifs in regions of reduced histone acetylation suggesting an important role in leukaemogenic transcriptional reprogramming. Forced re-expression of Gata2 was not compatible with sustained growth of leukaemic cells thus suggesting a previously unrecognised role for Gata2 in downregulation during the development of AML. Additionally, large scale human AML datasets revealed significantly higher expression of GATA2 in CD34+ cells from healthy controls compared with AML blast cells. The integrated genome-scale analysis applied in this study represents a valuable and widely applicable approach to study the transcriptional control of both normal and aberrant haematopoiesis and to identify critical factors responsible for transcriptional reprogramming in human cancer.


    Expression profiling by array on wild type lin-/kit+ bone marrow.
    GEO accession GSE25539

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