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

被引:33
作者
Kim, H
Bae, Y
Jeong, W
Ahn, C
Kang, SM [1 ]
机构
[1] Korea Univ, Grad Sch Biotechnol, Seoul 136701, South Korea
[2] Seoul Natl Univ, Coll Med, Seoul 110744, South Korea
关键词
ADPKD; PKD1; antisense oligonucleotides; p53;
D O I
10.1038/sj.ejhg.5201136
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:433 / 440
页数:8
相关论文
共 30 条
[1]   A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes [J].
Ariza, M ;
Alvarez, V ;
Marin, R ;
Aguado, S ;
LopezLarrea, C ;
Alvarez, J ;
Menendez, MJ ;
Coto, E .
JOURNAL OF MEDICAL GENETICS, 1997, 34 (07) :587-589
[2]   Characterization of microsatellite markers adjacent to AP-4 on chromosome 16p13.3 [J].
Bae, Y ;
Kim, H ;
Namgoong, H ;
Baek, M ;
Lee, J ;
Hwang, D ;
Hwang, Y ;
Ahn, C ;
Kang, S .
MOLECULAR AND CELLULAR PROBES, 2001, 15 (05) :313-315
[3]   PKD1 induces p21waf1 and regulation of the cell cycle via direct activation of the JAK-STAT signaling pathway in a process requiring PKD2 [J].
Bhunia, AK ;
Piontek, K ;
Boletta, A ;
Liu, LJ ;
Qian, F ;
Xu, PN ;
Germino, FJ ;
Germino, GG .
CELL, 2002, 109 (02) :157-168
[4]   The structure of a PKD domain from polycystin-1: Implications for polycystic kidney disease [J].
Bycroft, M ;
Bateman, A ;
Clarke, J ;
Hamill, SJ ;
Sandford, R ;
Thomas, RL ;
Chothia, C .
EMBO JOURNAL, 1999, 18 (02) :297-305
[5]   Role of the matrix in autosomal dominant polycystic kidney disease [J].
Carone, FA ;
Bacallao, R ;
Kanwar, Y .
RENAL FAILURE, 1998, 20 (02) :181-189
[6]  
CONSTANTINOUDELTAS CD, 1995, HUM GENET, V95, P416
[7]   EVIDENCE FOR A 3RD GENETIC-LOCUS FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE [J].
DAOUST, MC ;
REYNOLDS, DM ;
BICHET, DG ;
SOMLO, S .
GENOMICS, 1995, 25 (03) :733-736
[8]   HEPATIC CYSTS IN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE [J].
EVERSON, GT .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1993, 22 (04) :520-525
[9]   Antisense-induced down-regulation of thymidylate synthase and enhanced cytotoxicity of 5-FUdR in 5-FUdR-resistant HeLa cells [J].
Ferguson, PJ ;
DeMoor, JM ;
Vincent, MD ;
Koropatnick, J .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 134 (07) :1437-1446
[10]   The etiology, pathogenesis, and treatment of autosomal dominant polycystic kidney disease: Recent advances [J].
Grantham, JJ .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 28 (06) :788-803