Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development

Here we used RNA sequencing to characterize the transcriptional profile of the total RNA from c-Kit+ cells of Runx1 KO and control mice. Overall design: For bulk RNA-sequencing: Total RNA from c-Kit+ cells was extracted with AllPrep DNA/RNA/Protein Mini Kit (QIAGEN). Poly-A selected stranded mRNA libraries were constructed using the Illumina TruSeq Stranded mRNA Sample Prep Kits according to manufacturer's instructions. Unique barcode adapters were applied to each library. All libraries were combined in equimolar proportion into one pool for sequencing with a HiSeq2500 sequencer.