“…Pescadillo was isolated as a mutation affecting embryonic development (Allende et al+, 1996) and a mutant allele of the yeast gene resulted in growth arrest in G2 (Kinoshita et al+, 2001), consistent with a specific defect in cell-cycle progression+ Yeast Yhp1p/Nop7p is also reported to interact with Yvh1p (Sakumoto et al+, 2001), a protein-tyrosine phosphatase with a postulated role in the regulation of sporulation and meiosis+ There are clear precedents for proteins that function both in cell-cycle progression and ribosome synthesis+ Exit from mitosis in budding yeast requires a group of proteins, including the phosphatase Cdc14p, which down-regulate cyclin-dependent kinase activity+ Cdc14p is sequestered in the nucleolus in the RENT (regulator of nucleolar silencing and telophase) complex with Sir2p and Net1p, which serves to anchor the complex (Shou et al+, 1999)+ In addition, Net1p is required for the maintenance of normal nucleolar structure and its binding stimulates RNA polymerase I (Shou et al+, 1999(Shou et al+, , 2001)+ These nucleolus-specific functions of Net1p can be separated genetically from its cell-cycle functions in the RENT complex+ In human cells, the nucleolar p14/ARF protein binds and sequesters the negative regulator of p53 activity, Mdm2 (Tao & Levine, 1999;Weber et al+, 1999;Zhang & Xiong, 1999)+ Free Mdm2 ubiquitinates p53 and transports it to the cytoplasm where it is degraded by the proteosome (Fuchs et al+, 1998;Geyer et al+, 2000), and the nucleolar sequestration of Mdm2 contributes to the inhibition of this activity by ARF+ Mouse Pescadillo was identified by its up-regulation in cells lacking p53 (Kinoshita et al+, 2001), but other interactions with the p53 system have not been reported+…”