Senescence-inducing stress promotes proteolysis of phosphoglycerate mutase via ubiquitin ligase Mdm2.

Senescence-inducing stress promotes proteolysis of phosphoglycerate mutase via ubiquitin ligase Mdm2.
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衰老诱导应激通过泛素连接酶 Mdm2 促进磷酸甘油酸变位酶的蛋白水解。

DOI:
10.1083/jcb.201306149
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发表时间:
2014-03-03
期刊:
The Journal of cell biology
影响因子:
--
通讯作者:
Kondoh H
Kondoh H
中科院分区:
其他
文献类型:
--
作者:
Mikawa T;Maruyama T;Okamoto K;Nakagama H;Lleonart ME;Tsusaka T;Hori K;Murakami I;Izumi T;Takaori-Kondo A;Yokode M;Peters G;Beach D;Kondoh H

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Mdm 2是一种泛素连接酶和p53的下游效应子,在衰老诱导应激下通过泛素化和糖酵解酶PGAM的降解来减弱原代细胞的增殖潜力。尽管瓦尔堡效应的临床意义得到了充分的证明,但肿瘤细胞的积极糖酵解速率如何导致癌症的其他标志,如衰老旁路,仍不清楚。在这里,我们报告说,在癌基因或DNA损伤诱导的衰老,Pak1介导的磷酸甘油酸酯(PGAM)的磷酸化倾向于糖酵解酶泛素介导的降解。我们确定Mdm 2作为直接结合伙伴和泛素连接酶PGAM在培养细胞和体外。PGAM和Mdm 2的突变,废除PGAM的泛素化恢复了原代细胞在应激条件下的增殖潜力,并促进肿瘤转化。我们认为,Mdm 2,p53的下游效应,减弱瓦尔堡效应通过泛素化和降解PGAM。
Mdm2, a ubiquitin ligase and downstream effector of p53, attenuates the proliferative potential of primary cells via ubiquitination and degradation of the glycolytic enzyme PGAM under senescence-inducing stress. Despite the well-documented clinical significance of the Warburg effect, it remains unclear how the aggressive glycolytic rates of tumor cells might contribute to other hallmarks of cancer, such as bypass of senescence. Here, we report that, during oncogene- or DNA damage–induced senescence, Pak1-mediated phosphorylation of phosphoglycerate mutase (PGAM) predisposes the glycolytic enzyme to ubiquitin-mediated degradation. We identify Mdm2 as a direct binding partner and ubiquitin ligase for PGAM in cultured cells and in vitro. Mutations in PGAM and Mdm2 that abrogate ubiquitination of PGAM restored the proliferative potential of primary cells under stress conditions and promoted neoplastic transformation. We propose that Mdm2, a downstream effector of p53, attenuates the Warburg effect via ubiquitination and degradation of PGAM.
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