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- W2034873053 abstract "Antizymes (AZs) are polyamine-induced proteins that negatively regulate cellular polyamine synthesis and uptake. Three antizyme isoforms are conserved among mammals. AZ1 and AZ2 have a broad tissue distribution, while AZ3 is testis specific. Both AZ1 and AZ2 inhibit ornithine decarboxylase (ODC) activity by binding to ODC monomer and target it to the 26S proteasome at least in vivo. Both also inhibit extra-cellular polyamine uptake. Despite their being indistinguishable by these criteria, we show here using enhanced green fluorescent protein (EGFP)-AZ2 fusion protein that in mammalian cells, the subcellular location of AZ2 is mainly in the nucleus, and is different from that of AZ1. The C-terminal part of AZ2 is necessary for the nuclear distribution. Within a few hours, a shift in the distribution of EGFP-AZ2 fusion protein from cytoplasm to the nucleus or from nucleus to cytoplasm is observable in NIH3T3 cells. In addition, we found that in cells a majority of AZ2, but not AZ1, is phosphorylated at Ser-186, likely by protein kinase CK2. There may be a specific function of AZ2 in the nucleus." @default.
- W2034873053 created "2016-06-24" @default.
- W2034873053 creator A5017026237 @default.
- W2034873053 creator A5018586070 @default.
- W2034873053 creator A5025868058 @default.
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- W2034873053 date "2009-11-01" @default.
- W2034873053 modified "2023-09-24" @default.
- W2034873053 title "Subcellular localization and phosphorylation of antizyme 2" @default.
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- W2034873053 doi "https://doi.org/10.1002/jcb.22334" @default.
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