[HTML][HTML] Depletion of PKD1 by an antisense oligodeoxynucleotide induces premature G1/S-phase transition

H Kim, Y Bae, W Jeong, C Ahn, S Kang - European journal of human …, 2004 - nature.com
H Kim, Y Bae, W Jeong, C Ahn, S Kang
European journal of human genetics, 2004nature.com
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the growth of
epithelial cells and the influx of cyst fluid. The 14-kb mRNA of the polycystic kidney disease
gene, PKD1, encodes the polycystin-1 protein, whose function remains unknown. In this
study, we observed that polycystin-1 localized in epithelial cell–cell contacts of 293 cells. We
found, by bromodeoxyuridine (BrdU) incorporation experiments and Western blot analysis of
S-phase-specific cyclins, that the depletion of polycystin-1 led to an increased cell …
Abstract
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the growth of epithelial cells and the influx of cyst fluid. The 14-kb mRNA of the polycystic kidney disease gene, PKD1, encodes the polycystin-1 protein, whose function remains unknown. In this study, we observed that polycystin-1 localized in epithelial cell–cell contacts of 293 cells. We found, by bromodeoxyuridine (BrdU) incorporation experiments and Western blot analysis of S-phase-specific cyclins, that the depletion of polycystin-1 led to an increased cell proliferation rate and caused a premature G1/S-phase transition. In addition, we showed that the depletion of polycystin-1 reduced the amount of p53 in 293 cells irradiated by UV light, suggesting that polycystin-1 acts as a regulator of G1 checkpoint, which controls entry into the S phase and prevents the replication of damaged DNA. Our results might provide an insight into the formation and progression of ADPKD cysts.
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