Phosphoinositide-specific phospholipase C beta1b (PI-PLCbeta1b) interactome: affinity purification-mass spectrometry analysis of PI-PLCbeta1b with nuclear protein (Articolo in rivista)

Type
Label
  • Phosphoinositide-specific phospholipase C beta1b (PI-PLCbeta1b) interactome: affinity purification-mass spectrometry analysis of PI-PLCbeta1b with nuclear protein (Articolo in rivista) (literal)
Anno
  • 2013-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1074/mcp.M113.029686 (literal)
Alternative label
  • Piazzi M, Blalock WL, Bavelloni A, Faenza I, D'Angelo A, Maraldi NM, Cocco L (2013)
    Phosphoinositide-specific phospholipase C beta1b (PI-PLCbeta1b) interactome: affinity purification-mass spectrometry analysis of PI-PLCbeta1b with nuclear protein
    in Molecular & cellular proteomics (Online)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Piazzi M, Blalock WL, Bavelloni A, Faenza I, D'Angelo A, Maraldi NM, Cocco L (literal)
Pagina inizio
  • 2220 (literal)
Pagina fine
  • 2235 (literal)
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  • http://www.mcponline.org/content/12/8/2220.long (literal)
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  • 12 (literal)
Rivista
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  • 16 (literal)
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  • 8 (literal)
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  • Cell Signaling Laboratory, Department of Biomedical Science (DIBINEM), University of Bologna, Bologna, Italy; Institute of Molecular Genetics, National Research Council of Italy (IGM-CNR), Bologna, Italy; SC Laboratory of Musculoskeletal Cell Biology, Rizzoli Orthopedic Institute, Bologna, Italy; Laboratory RAMSES, Rizzoli Orthopedic Institute, Bologna, Italy (literal)
Titolo
  • Phosphoinositide-specific phospholipase C beta1b (PI-PLCbeta1b) interactome: affinity purification-mass spectrometry analysis of PI-PLCbeta1b with nuclear protein (literal)
Abstract
  • Two isoforms of inositide-dependent phospholipase C ?1 (PI-PLC?1) are generated by alternative splicing (PLC?1a and PLC?1b). Both isoforms are present within the nucleus, but in contrast to PLC?1a, the vast majority of PLC?1b is nuclear. In mouse erythroid leukemia cells, PI-PLC?1 is involved in the regulation of cell division and the balance between cell proliferation and differentiation. It has been demonstrated that nuclear localization is crucial for the enzymatic function of PI-PLC?1, although the mechanism by which this nuclear import occurs has never been fully characterized. The aim of this study was to characterize both the mechanism of nuclear localization and the molecular function of nuclear PI-PLC?1 by identifying its interactome in Friend's erythroleukemia isolated nuclei, utilizing a procedure that coupled immuno-affinity purification with tandem mass spectrometry analysis. Using this procedure, 160 proteins were demonstrated to be in association with PI-PLC?1b, some of which have been previously characterized, such as the splicing factor SRp20 (Srsf3) and Lamin B (Lmnb1). Co-immunoprecipitation analysis of selected proteins confirmed the data obtained via mass spectrometry. Of particular interest was the identification of the nuclear import proteins Kpna2, Kpna4, Kpnb1, Ran, and Rangap1, as well as factors involved in hematological malignancies and several anti-apoptotic proteins. These data give new insight into possible mechanisms of nuclear trafficking and functioning of this critical signaling molecule. (literal)
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