【摘 要】
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PTEN tumor suppressor opposes the P13K/Akt signaling pathway in the cytoplasm and maintains chromosomal integrity in the nucleus.Nucleus-cytoplasm shuttling of
【机 构】
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Department of Cell Biology, The Municipal Key Laboratory for Liver Protection and Regulation of Rege
论文部分内容阅读
PTEN tumor suppressor opposes the P13K/Akt signaling pathway in the cytoplasm and maintains chromosomal integrity in the nucleus.Nucleus-cytoplasm shuttling of PTEN is regulated by ubiquitylation,SUMOylation and phosphorylation,and nuclear PTEN has been proposed to exhibit tumor-suppressive functions.Here we show that PTEN is conjugated by Nedd8 under high glucose conditions,which induces PTEN nuclear import without effects on PTEN stability.PTEN neddylation is promoted by the XIAP ligase and removed by the NEDP1 deneddylase.We identify Lys197 and Lys402 as major neddylation sites on PTEN.Neddylated PTEN accumulates predominantly in the nucleus and promotes rather than suppresses cell proliferation and metabolism.The nuclear neddylated PTEN dephosphorylates the fatty acid synthase (FASN) protein,inhibits the TRIM21-mediated ubiquitylation and degradation of FASN,and then promotes de novo fatty acid synthesis.In human breast cancer tissues,neddylated PTEN correlates with tumor progression and poor prognosis.Therefore,we demonstrate a previously unidentified pool of nuclear PTEN in the Nedd8-conjugated form and an unexpected tumor-promoting role of neddylated PTEN.
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