PTEN regulates Mdm2 expression through the P1 promoter
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作者:
Chang, CJ
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Univ Calif Los Angeles, Sch Med, Howard Hughes Med Inst, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Sch Med, Howard Hughes Med Inst, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
Chang, CJ
[1
]
Freeman, DJ
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Univ Calif Los Angeles, Sch Med, Howard Hughes Med Inst, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Sch Med, Howard Hughes Med Inst, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
Freeman, DJ
[1
]
Wu, H
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Univ Calif Los Angeles, Sch Med, Howard Hughes Med Inst, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Sch Med, Howard Hughes Med Inst, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
Wu, H
[1
]
机构:
[1] Univ Calif Los Angeles, Sch Med, Howard Hughes Med Inst, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
MDM2 is an oncoprotein that controls tumorigenesis through both p53-dependent and - independent mechanisms. Mdm2 mRNA level is transcriptionally regulated by p53 in response to stress such as DNA damage, and its protein level and subcellular localization are post-translationally modulated by the AKT serine/threonine kinase. Previous studies showed that PTEN, a dual specificity phosphatase that antagonizes phosphatidylinositol 3-kinase/ AKT signaling, is capable of blocking MDM2 nuclear translocation and destabilizing the MDM2 protein. Results from our current study demonstrate an additional role for PTEN in regulating MDM2 functions; PTEN modulates Mdm2 transcription and isoform selection by negatively regulating its P1 promoter. In Pten-null cell lines and prostate cancer tissues, Mdm2 P1 promoter activity is up-regulated, resulting in increased L-Mdm2 expression and enhanced p90(MDM2) isoform production. Furthermore, PTEN controls Mdm2 P1 promoter activity through its lipid phosphatase activity, independent of p53. Thus, our results provide a novel mechanism for PTEN in controlling MDM2 oncoprotein functions.