RT Journal A1 Arnold, Christopher P. A1 Tan, Ruoying A1 Zhou, Baiyu A1 Yue, Si-Biao A1 Schaffert, Steven A1 Biggs, Joseph R. A1 Doyonnas, Regis A1 Lo, Miao-Chia A1 Perry, John M. A1 Renault, Valérie M. A1 Sacco, Alessandra A1 Somervaille, Tim A1 Viatour, Patrick A1 Brunet, Anne A1 Cleary, Michael L. A1 Li, Linheng A1 Sage, Julien A1 Zhang, Dong-Er A1 Blau, Helen M. A1 Chen, Caifu A1 Chen, Chang-Zheng T1 MicroRNA programs in normal and aberrant stem and progenitor cells JF Genome Research JO Genome Research YR 2011 FD May 01 VO 21 IS 5 SP 798 OP 810 DO 10.1101/gr.111385.110 UL http://genome.cshlp.org/content/21/5/798.abstract AB Emerging evidence suggests that microRNAs (miRNAs), an abundant class of ∼22-nucleotide small regulatory RNAs, play key roles in controlling the post-transcriptional genetic programs in stem and progenitor cells. Here we systematically examined miRNA expression profiles in various adult tissue-specific stem cells and their differentiated counterparts. These analyses revealed miRNA programs that are common or unique to blood, muscle, and neural stem cell populations and miRNA signatures that mark the transitions from self-renewing and quiescent stem cells to proliferative and differentiating progenitor cells. Moreover, we identified a stem/progenitor transition miRNA (SPT-miRNA) signature that predicts the effects of genetic perturbations, such as loss of PTEN and the Rb family, AML1-ETO9a expression, and MLL-AF10 transformation, on self-renewal and proliferation potentials of mutant stem/progenitor cells. We showed that some of the SPT-miRNAs control the self-renewal of embryonic stem cells and the reconstitution potential of hematopoietic stem cells (HSCs). Finally, we demonstrated that SPT-miRNAs coordinately regulate genes that are known to play roles in controlling HSC self-renewal, such as Hoxb6 and Hoxa4. Together, these analyses reveal the miRNA programs that may control key processes in normal and aberrant stem and progenitor cells, setting the foundations for dissecting post-transcriptional regulatory networks in stem cells.