TY - JOUR T1 - IL-6 Enhances the Nuclear Translocation of DNA Cytosine-5-Methyltransferase 1 (DNMT1) <em>via</em> Phosphorylation of the Nuclear Localization Sequence by the AKT Kinase JF - Cancer Genomics - Proteomics JO - Cancer Genomics Proteomics SP - 387 LP - 398 VL - 4 IS - 6 AU - DAVID R. HODGE AU - EDWARD CHO AU - TERRY D. COPELAND AU - TAD GUSZCZYNSKI AU - ERIC YANG AU - ARUN K. SETH AU - WILLIAM L. FARRAR Y1 - 2007/11/01 UR - http://cgp.iiarjournals.org/content/4/6/387.abstract N2 - The epigenetic programming of genomic DNA is accomplished, in part, by several DNA cytosine-5-methyltransferases that act by covalently modifying cytosines with the addition of a methyl group. This covalent modification is maintained by the DNA cytosine-5-methyltransferase-1 enzyme (DNMT1), which is capable of acting in concert with other similar enzymes to silence important tumor suppressor genes. IL-6 is a multifunctional mediator of inflammation, acting through several major signaling cascades, including the phosphatidylinositol-3-kinase pathway (PI-3-K), which activates protein kinase B (AKT/PKB) downstream. Here, we show that the subcellular localization of DNMT1 can be altered by the addition of IL-6, increasing the rate of nuclear translocation of the enzyme from the cytosolic compartment. The mechanism of nuclear translocation of DNMT1 is greatly enhanced by phosphorylation of the DNMT1 nuclear localization signal (NLS) by PKB/AKT kinase. Mutagenic alteration of the two AKT target amino acids within the NLS results in a major loss of DNMT1 nuclear translocation, while the creation of a “phospho-mimic” amino acid (mutation to acidic residues) restores this compartmentation ability. These observations suggest an interesting hypothesis regarding how mediators of chronic inflammation may disturb the delicate balance of cellular compartmentalization of important proteins, and reveals a potential mechanism for the induction or enhancement of tumor growth via alteration of the components involved in the epigenetic programming of a cell. ER -