In vivo interference with Skp1 function leads to genetic instability and neoplastic transformation

Skp1 is involved in a variety of crucial cellular functions, among which the best understood is the formation together with Cull of Skp1-cullin-F-box protein ubiquitin ligases. To investigate the role of Skp1, we generated transgenic (Tg) mice expressing a Cull deletion mutant (CulI-N252) able to sequestrate and inactivate Skp1. In vivo interference with Skp1 function through expression of the CulI-N252 mutant into the T-cell lineage results in lymphoid organ hypoplasia and reduced proliferation. Nonetheless, after a period of latency, CulI-N252 Tg mice succumb to T-cell lymphomas with high penetrance (>80%). Both T-cell depletion and the neoplastic phenotype of CulI-N252 Tg mice are largely rescued in CulI-N252, Skp1 double-Tg mice, indicating that the effects of CulI-N252 are due to a sequestration of the endogenous Skp1. Analysis of CulI-N252 lymphomas demonstrates striking karyotype heterogeneity associated with c-myc amplification and c-Myc overexpression. We show that the in vitro expression of the CulI-N252 mutant causes a pleiotrophic phenotype, which includes the formation of multinucleated cells, centrosome and mitotic spindle abnormalities, and impaired chromosome segregation. Our findings support a crucial role for Skp1 in proper chromosomal segregation, which is required for the maintenance of euploidy and suppression of transformation.