Novel properties of the nucleolar targeting signal of human angiogenin

Rui Lixin, Athina Efthymiadis, Beric Henderson, David A. Jans

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45 Citations (Scopus)

Abstract

The polypeptide ligand angiogenin, a potent inducer of angiogenesis, localizes in the nucleus/nucleolus subsequent to endocytosis by relevant cell types. This study examines the kinetic properties of the nucleolar targeting signal (NTS) of angiogenin (IMRRRGL35) at the single cell level. We show that the NTS is sufficient to target green fluorescent protein (GFP), but not β-galactosidase, to the nucleolus of rat hepatoma cells. Mutation of Arg33 to Ala within the NTS abolishes targeting activity. Nuclear/nucleolar import conferred by the NTS of angiogenin is reduced by cytosolic factors as well as ATP and is independent of importins and Ran. The NTS also confers the ability to bind to nuclear/nucleolar components which is inhibited by ATP hydrolysis; nonhydrolysable GTP analogs prevent nuclear accumulation in the absence of an intact nuclear envelope through an apparent cytoplasmic retention mechanism. Since the lectin wheat germ agglutinin does not inhibit transport, we postulate a mechanism for angiogenin nuclear/nucleolar import involving passive diffusion of angiogenin through the nuclear pore and NTS-mediated nuclear/nucleolar retention, and with cytoplasmic retention modulating the process. This pathway is clearly distinct from that of conventional signal-mediated nuclear protein import.

Original languageEnglish
Pages (from-to)185-193
Number of pages9
JournalBiochemical and Biophysical Research Communications
Volume284
Issue number1
DOIs
Publication statusPublished - 14 Oct 2001
Externally publishedYes

Keywords

  • Angiogenic factors
  • Nuclear protein import
  • Nucleolus
  • Targeting signal

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