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A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity.

机译:用于Oct4调节剂的基因组规模的RNAi筛选定义了Paf1复合物对于胚胎干细胞身份的作用。

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摘要

Pluripotent embryonic stem cells (ESCs) maintain self-renewal while ensuring a rapid response to differentiation cues. The identification of genes maintaining ESC identity is important to develop these cells for their potential therapeutic use. Here we report a genome-scale RNAi screen for a global survey of genes affecting ESC identity via alteration of Oct4 expression. Factors with the strongest effect on Oct4 expression included components of the Paf1 complex, a protein complex associated with RNA polymerase II. Using a combination of proteomics, expression profiling, and chromatin immunoprecipitation, we demonstrate that the Paf1C binds to promoters of key pluripotency genes, where it is required to maintain a transcriptionally active chromatin structure. The Paf1C is developmentally regulated and blocks ESC differentiation upon overexpression, and the knockdown in ESCs causes expression changes similar to Oct4 or Nanog depletions. We propose that the Paf1C plays an important role in maintaining ESC identity.
机译:多能胚胎干细胞(ESC)保持自我更新,同时确保对分化线索的快速反应。维持ESC身份的基因的鉴定对于开发这些细胞的潜在治疗用途很重要。在这里,我们报告了通过Oct4表达改变影响ESC身份的基因的全球调查的基因组规模的RNAi筛选。对Oct4表达影响最大的因素包括Paf1复合物的成分,该复合物是与RNA聚合酶II相关的蛋白质复合物。使用蛋白质组学,表达谱和染色质免疫沉淀的组合,我们证明Paf1C绑定到关键多能性基因的启动子,在那里需要维持转录活性染色质结构。 Paf1C受发育调节,并在过表达时阻止ESC分化,而敲低ESC会导致表达变化类似于Oct4或Nanog耗竭。我们建议Paf1C在维护ESC身份中起重要作用。

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