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首页> 外文期刊>Nature Communications >Mitochondrial E3 ligase March5 maintains stemness of mouse ES cells via suppression of ERK signalling
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Mitochondrial E3 ligase March5 maintains stemness of mouse ES cells via suppression of ERK signalling

机译:线粒体E3连接酶March5通过抑制ERK信号传导维持小鼠ES细胞的干性

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Embryonic stem cells (ESCs) possess pluripotency, which is the capacity of cells to differentiate into all lineages of the mature organism. Increasing evidence suggests that the pluripotent state of ESCs is regulated by a combination of extrinsic and intrinsic factors. The underlying mechanisms, however, are not completely understood. Here, we show that March5, an E3 ubiquitin ligase, is involved in maintaining mouse-ESC (mESC) pluripotency. Knockdown of March5 in mESCs led to differentiation from naive pluripotency. Mechanistically, as a transcriptional target of Klf4, March5 catalyses K63-linked polyubiquitination of Prkar1a, a negative regulatory subunit of PKA, to activate PKA, thereby inhibiting the Raf/MEK/ERK pathway. Moreover, March5 is able to replace a MEK/ERK inhibitor to maintain mESC pluripotency under serum-free culture conditions. In addition, March5 can partially replace the use of Klf4 for somatic cell reprogramming. Collectively, our study uncovers a role for the Klf4-March5-PKA-ERK pathway in maintaining the stemness properties of mESCs.
机译:胚胎干细胞(ESC)具有多能性,这是细胞分化为成熟生物的所有谱系的能力。越来越多的证据表明,ESC的全能状态受外在因素和内在因素共同调节。但是,尚未完全理解其基本机制。在这里,我们显示E3泛素连接酶March5与维持小鼠ESC(mESC)多能性有关。 mESCs中3月5日的敲低导致与幼稚多能性的区别。从机理上讲,March5作为Klf4的转录靶点,催化K63连接的Prkar1a(PKA的负调节亚基)的多泛素化,激活PKA,从而抑制Raf / MEK / ERK途径。此外,March5能够代替MEK / ERK抑制剂在无血清培养条件下维持mESC多能性。此外,March5可以部分替代使用Klf4进行体细胞重编程。总的来说,我们的研究揭示了Klf4-March5-PKA-ERK途径在维持mESCs的干性中的作用。

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