Nucleophosmin is required for DNA integrity and p19Arf protein stability.

TY - JOUR

T1 - Nucleophosmin is required for DNA integrity and p19Arf protein stability.

AU - Colombo, Emanuela

AU - Bonetti, Paola

AU - Lazzerini Denchi, Eros

AU - Martinelli, Paola

AU - Zamponi, Raffaella

AU - Marine, Jean-Christophe

AU - Helin, Kristian

AU - Falini, Brunangelo

AU - Pelicci, Pier Giuseppe

N1 - Keywords: Animals; Apoptosis; Base Sequence; Cell Nucleolus; Cell Proliferation; Cells, Cultured; Cyclin-Dependent Kinase Inhibitor p16; DNA; DNA Damage; Drug Stability; Female; Fetal Death; Genes, p53; Mice; Mice, Inbred C57BL; Mice, Knockout; Nuclear Proteins; Pregnancy; Tumor Suppressor Protein p14ARF; Tumor Suppressor Protein p53

PY - 2005

Y1 - 2005

N2 - Nucleophosmin (NPM) is a nucleolar phosphoprotein that binds the tumor suppressors p53 and p19(Arf) and is thought to be indispensable for ribogenesis, cell proliferation, and survival after DNA damage. The NPM gene is the most frequent target of genetic alterations in leukemias and lymphomas, though its role in tumorigenesis is unknown. We report here the first characterization of a mouse NPM knockout strain. Lack of NPM expression results in accumulation of DNA damage, activation of p53, widespread apoptosis, and mid-stage embryonic lethality. Fibroblasts explanted from null embryos fail to grow and rapidly acquire a senescent phenotype. Transfer of the NPM mutation into a p53-null background rescued apoptosis in vivo and fibroblast proliferation in vitro. Cells null for both p53 and NPM grow faster than control cells and are more susceptible to transformation by activated oncogenes, such as mutated Ras or overexpressed Myc. In the absence of NPM, Arf protein is excluded from nucleoli and is markedly less stable. Our data demonstrate that NPM regulates DNA integrity and, through Arf, inhibits cell proliferation and are consistent with a putative tumor-suppressive function of NPM.

AB - Nucleophosmin (NPM) is a nucleolar phosphoprotein that binds the tumor suppressors p53 and p19(Arf) and is thought to be indispensable for ribogenesis, cell proliferation, and survival after DNA damage. The NPM gene is the most frequent target of genetic alterations in leukemias and lymphomas, though its role in tumorigenesis is unknown. We report here the first characterization of a mouse NPM knockout strain. Lack of NPM expression results in accumulation of DNA damage, activation of p53, widespread apoptosis, and mid-stage embryonic lethality. Fibroblasts explanted from null embryos fail to grow and rapidly acquire a senescent phenotype. Transfer of the NPM mutation into a p53-null background rescued apoptosis in vivo and fibroblast proliferation in vitro. Cells null for both p53 and NPM grow faster than control cells and are more susceptible to transformation by activated oncogenes, such as mutated Ras or overexpressed Myc. In the absence of NPM, Arf protein is excluded from nucleoli and is markedly less stable. Our data demonstrate that NPM regulates DNA integrity and, through Arf, inhibits cell proliferation and are consistent with a putative tumor-suppressive function of NPM.

U2 - 10.1128/MCB.25.20.8874-8886.2005

DO - 10.1128/MCB.25.20.8874-8886.2005

M3 - Journal article

C2 - 16199867

SN - 0270-7306

VL - 25

SP - 8874

EP - 8886

JO - Molecular and Cellular Biology

JF - Molecular and Cellular Biology

IS - 20

ER -