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Identification of importin alpha 7 specific transport cargoes using a proteomic screening approach

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Item Type:Article
Title:Identification of importin alpha 7 specific transport cargoes using a proteomic screening approach
Creators Name:Hügel, S. and Depping, R. and Dittmar, G. and Rother, F. and Cabot, R. and Sury, M.D. and Hartmann, E. and Bader, M.
Abstract:The importin alpha:beta complex is responsible for the nuclear import of proteins bearing classical nuclear localization signals. In mammals several importin alpha subtypes are known to exist which are suggested to have individual functions. Importin alpha 7 was shown to play a crucial role in early embryo development in mice. Embryos from importin alpha 7 depleted females stop at the two-cell stage and show disturbed zygotic genome activation. Since there is evidence that individual importin alpha subtypes possess cargo specificities, we hypothesized that importin alpha 7 binds a unique set of intracellular proteins. By using a collection of in vitro and in vivo binding assays, importin alpha 7 interaction partners were identified that differed from proteins found to bind to importin alpha 2 and 3. One of the proteins preferentially binding importin alpha 7 was the maternal effect protein Brg1. However, Brg1 was localized in oocyte nuclei in importin alpha 7 deficient embryos, albeit in reduced amounts, suggesting additional modes of nuclear translocation of this factor. An additional SILAC based screening approach identified Ash2l, Chd3, Mcm3, and Smarcc1 whose nuclear import seems to be disturbed in importin alpha 7 deficient fibroblasts.
Keywords:Importin alpha, Karyopherin alpha, Nucleocytoplasmic Transport, Brg1, smarca4, Baf190a, Ash2l, Chd3, Mcm3, Mcm5, Smarcc1, Binding Partners, Animals, Mice
Source:Molecular & Cellular Proteomics
ISSN:1535-9476
Publisher:American Society for Biochemistry and Molecular Biology
Volume:13
Number:5
Page Range:1286-1298
Date:1 May 2014
Official Publication:https://doi.org/10.1074/mcp.M112.026856
PubMed:View item in PubMed

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