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首页> 外文期刊>Nature Communications >A Lin28 homologue reprograms differentiated cells to stem cells in the moss Physcomitrella patens
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A Lin28 homologue reprograms differentiated cells to stem cells in the moss Physcomitrella patens

机译:Lin28同源物可将苔藓植物Physcomitrella patens中的分化细胞重编程为干细胞

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摘要

Both land plants and metazoa have the capacity to reprogram differentiated cells to stem cells. Here we show that the moss Physcomitrella patens Cold-Shock Domain Protein 1 (PpCSP1) regulates reprogramming of differentiated leaf cells to chloronema apical stem cells and shares conserved domains with the induced pluripotent stem cell factor Lin28 in mammals. PpCSP1 accumulates in the reprogramming cells and is maintained throughout the reprogramming process and in the resultant stem cells. Expression of PpCSP1 is negatively regulated by its 3′-untranslated region (3′-UTR). Removal of the 3′-UTR stabilizes PpCSP1 transcripts, results in accumulation of PpCSP1 protein and enhances reprogramming. A quadruple deletion mutant of PpCSP1 and three closely related PpCSP genes exhibits attenuated reprogramming indicating that the PpCSP genes function redundantly in cellular reprogramming. Taken together, these data demonstrate a positive role of PpCSP1 in reprogramming, which is similar to the function of mammalian Lin28.
机译:陆地植物和后生动物都具有将分化细胞重编程为干细胞的能力。在这里,我们显示了苔藓小立碗藓冷休克结构域蛋白1(PpCSP1)调节分化的叶细胞向叶绿体顶端干细胞的重编程,并在哺乳动物中与诱导的多能干细胞因子Lin28共享保守的结构域。 PpCSP1积累在重编程细胞中,并在整个重编程过程中和所得干细胞中得到维持。 PpCSP1的表达受到其3'非翻译区(3'-UTR)的负调控。 3'-UTR的去除稳定了PpCSP1转录物,导致了PpCSP1蛋白的积累并增强了重新编程。 PpCSP1的四个删除突变体和三个密切相关的PpCSP基因表现出减弱的重编程,这表明PpCSP基因在细胞重编程中具有多余的功能。综上所述,这些数据证明了PpCSP1在重编程中具有积极作用,与哺乳动物Lin28的功能相似。

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