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A Genome-Wide RNAi Screen Reveals MAP Kinase Phosphatases as Key ERK Pathway Regulators during Embryonic Stem Cell Differentiation

机译:全基因组RNAi屏幕揭示了MAP激酶磷酸酶作为胚胎干细胞分化过程中的关键ERK途径调节剂。

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摘要

Embryonic stem cells and induced pluripotent stem cells represent potentially important therapeutic agents in regenerative medicine. Complex interlinked transcriptional and signaling networks control the fate of these cells towards maintenance of pluripotency or differentiation. In this study we have focused on how mouse embryonic stem cells begin to differentiate and lose pluripotency and, in particular, the role that the ERK MAP kinase and GSK3 signaling pathways play in this process. Through a genome-wide siRNA screen we have identified more than 400 genes involved in loss of pluripotency and promoting the onset of differentiation. These genes were functionally associated with the ERK and/or GSK3 pathways, providing an important resource for studying the roles of these pathways in controlling escape from the pluripotent ground state. More detailed analysis identified MAP kinase phosphatases as a focal point of regulation and demonstrated an important role for these enzymes in controlling ERK activation kinetics and subsequently determining early embryonic stem cell fate decisions.
机译:胚胎干细胞和诱导性多能干细胞是再生医学中潜在的重要治疗剂。复杂的互连转录和信号网络控制着这些细胞的命运,以维持多能性或分化。在这项研究中,我们集中于小鼠胚胎干细胞如何开始分化和丧失多能性,尤其是ERK MAP激酶和GSK3信号通路在此过程中的作用。通过全基因组siRNA筛选,我们已经鉴定出400多个基因与多能性丧失和促进分化的发生有关。这些基因在功能上与ERK和/或GSK3途径相关,为研究这些途径在控制多能性基态逃逸中的作用提供了重要资源。更详细的分析确定了MAP激酶磷酸酶为调控的重点,并证明了这些酶在控制ERK激活动力学并随后确定早期胚胎干细胞命运的决定中的重要作用。

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