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正常和异常干细胞及祖细胞中的 microRNA 程序。

MicroRNA programs in normal and aberrant stem and progenitor cells.

机构信息

Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305, USA.

出版信息

Genome Res. 2011 May;21(5):798-810. doi: 10.1101/gr.111385.110. Epub 2011 Mar 30.

Abstract

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.

摘要

新出现的证据表明,微 RNA(miRNA)是一类丰富的约 22 个核苷酸的小调控 RNA,在控制干细胞和祖细胞的转录后遗传程序中发挥关键作用。在这里,我们系统地检查了各种成人组织特异性干细胞及其分化对应物中的 miRNA 表达谱。这些分析揭示了血液、肌肉和神经干细胞群体中常见或独特的 miRNA 程序,以及标志着从自我更新和静止干细胞向增殖和分化祖细胞转变的 miRNA 特征。此外,我们确定了一个干细胞/祖细胞转化 miRNA(SPT-miRNA)特征,该特征可预测遗传干扰(如缺失 PTEN 和 Rb 家族、AML1-ETO9a 表达和 MLL-AF10 转化)对突变干细胞/祖细胞自我更新和增殖潜力的影响。我们表明,一些 SPT-miRNAs 控制胚胎干细胞的自我更新和造血干细胞(HSCs)的重建潜力。最后,我们证明 SPT-miRNAs 协调调控已知在控制 HSC 自我更新中起作用的基因,如 Hoxb6 和 Hoxa4。总之,这些分析揭示了可能控制正常和异常干细胞和祖细胞中关键过程的 miRNA 程序,为解析干细胞中转录后调控网络奠定了基础。

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