pRB and p107 have distinct effects when expressed in pRB-deficient tumor cells at physiologically relevant levels
pmid: 10951581
pRB and p107 have distinct effects when expressed in pRB-deficient tumor cells at physiologically relevant levels
A key difference among the three structurally similar pRB family members is that only pRB is a tumor suppressor. Identification of distinctive functional differences between pRB and p107/p130 therefore holds promise for a better understanding of the tumor suppression mechanisms of pRB. Enigmatically, pRB and p107 have been shown to have indistinguishable growth suppression activities when studied in the pRB-deficient Saos-2 cell system. In this study, we discovered that, when expressed at physiologically relevant levels, pRB and p107 had distinctive effects in causing growth suppression. pRB induced cellular p130 levels while p107 repressed them. p107, but not pRB, blocked cells inside S phase in addition to G1 arrest. In contrast, no qualitative differences were identified in their abilities to repress the expression of a set of suspected pRB/E2F repression target genes. These results indicate that pRB and p107 possess different growth suppression effects, despite the fact that they have similar E2F repression effects.
- Yeshiva University United States
- Albert Einstein College of Medicine United States
Osteosarcoma, Retinoblastoma-Like Protein p130, Cell Cycle, Cyclin-Dependent Kinase 2, Nuclear Proteins, Proteins, Bone Neoplasms, Cell Cycle Proteins, Retinoblastoma-Like Protein p107, Protein Serine-Threonine Kinases, Phosphoproteins, Retinoblastoma Protein, Cyclin-Dependent Kinases, E2F Transcription Factors, DNA-Binding Proteins, CDC2-CDC28 Kinases, Humans, Carrier Proteins, Transcription Factor DP1, Retinoblastoma-Binding Protein 1
Osteosarcoma, Retinoblastoma-Like Protein p130, Cell Cycle, Cyclin-Dependent Kinase 2, Nuclear Proteins, Proteins, Bone Neoplasms, Cell Cycle Proteins, Retinoblastoma-Like Protein p107, Protein Serine-Threonine Kinases, Phosphoproteins, Retinoblastoma Protein, Cyclin-Dependent Kinases, E2F Transcription Factors, DNA-Binding Proteins, CDC2-CDC28 Kinases, Humans, Carrier Proteins, Transcription Factor DP1, Retinoblastoma-Binding Protein 1
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