only four of the chromatin related group of genes was common to all populations whereas that of most of the others was batch-specific. The imprinted gene class was 9004-82-4 over-represented in the lists of induced genes in all four hMSC batches. Batch-dependent variation was reflected by the significance of the induction, batches 2 and 4 having lower p values than batches 1 and 3. A few imprinted genes were regulated in some populations only. Thus, MEST was repressed only in batches 1 and 3, DLK1 only in batches 2 and 4, and PEG3 only in batches 1 and 2. Other imprinted genes, such as TPP12 were also regulated in only a fraction of the populations but in opposite directions, being repressed in batch 2 and induced in batch 3. Global statistical analysis suggests that the experimentally confirmed imprinted genes affected by SYT-SSX1 in all MSCs include H19, CDKN1C, DLK1, DIRAS3 and IGF2 but that, remarkably, most of them show different expression profiles in the four cell batches, namely, strong induction in batch 4, more moderate induction in batches 1 and 2 and no induction in batch 3. These observations were validated by real time PCR for H19 and IGF2. Single batch gene expression analysis according to Gene Ontology annotation, revealed remarkable variation among the batches. The GO term nervous system development was also over-represented in batch 2 but not in batch 1 or 3, consistent with SYTSSX1- mediated pressure toward neuronal differentiation in some MSC populations only. Single population analysis also suggested a variable effect of SYT-SSX on the expression of genes encoding proteins that constitute components of the extracellular matrix, mediate cellextracellular matrix interactions, and participate in vascular development, angiogenesis, tissue remodeling and cell motion. In batch 3, GO term analysis suggests inhibition of expression of these genes. Similarly, in batch 1, the list of repressed genes included over-representation of the GO terms extracellular matrix, extracellular region, proteinaceous extracellular matrix, cell adhesion, integrin complex, integrin-mediated signaling pathway. By contrast, in batches 2 and 4, the GO terms cell adhesionand extracellular matrix were over-represented in the list of induced genes. Expression of these categories of proteins is important for the biological function of both 4-Thiazolecarboxamide,5-(3-methoxypropyl)-2-phenyl-N-[2-[6-(1-pyrrolidinylmethyl)thiazolo[5,4-b]pyridin-2-yl]phenyl]- (hydrochloride) cost normal and cancer stem cells, the former requiring release from their niche in the bone marrow in order to be recruited to target tis
