F-box protein Skp2: a novel transcriptional target of E2F

被引:113
作者
Zhang, L [1 ]
Wang, C [1 ]
机构
[1] Univ Illinois, Ctr Mol Biol Oral Dis, Chicago, IL 60612 USA
关键词
transcription; SCFskp2; E2F; cell cycle;
D O I
10.1038/sj.onc.1209286
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
The F-box-containing protein Skp2 plays a critical role in coordinating the G1/S transition and progression through the S phase of the mammalian cell cycle. Skp2 is overexpressed in a broad spectrum of human cancers and the expression level correlates with tumor malignancy. However, the Skp2 gene is neither amplified nor rearranged in most human cancers and the underlying mechanism of Skp2 overexpression remains poorly understood. We show here that the Skp2 gene contains a functional E2F response element ( hSRE2). Ectopic expression of E2F1 induces expression of the endogenous Skp2 gene in human fibroblast cells, whereas antisense-mediated knockdown of E2F1 in human tumor cell lines reduces expression of endogenous Skp2 gene. The hSRE2 element not only participates in activation of Skp2 promoter function during normal cell cycle progression into S phase, it is also required for the high-level Skp2 gene expression in many human tumor cell lines. These results reveal Skp2 as a novel target for E2F regulation that is disrupted in several human tumor cell lines.
引用
收藏
页码:2615 / 2627
页数:13
相关论文
共 65 条
[41]   Targeted disruption of Skp2 results in accumulation of cyclin E and p27Kip1, polyploidy and centrosome overduplication [J].
Nakayama, K ;
Nagahama, H ;
Minamishima, YA ;
Matsumoto, M ;
Nakamichi, I ;
Kitagawa, K ;
Shirane, M ;
Tsunematsu, R ;
Tsukiyama, T ;
Ishida, N ;
Kitagawa, M ;
Nakayama, K ;
Hatakeyama, S .
EMBO JOURNAL, 2000, 19 (09) :2069-2081
[42]   Skp2-mediated degradation of p27 regulates progression into mitosis [J].
Nakayama, K ;
Nagahama, H ;
Minamishima, YA ;
Miyake, S ;
Ishida, N ;
Hatakeyama, S ;
Kitagawa, M ;
Iemura, S ;
Natsume, T ;
Nakayama, KI .
DEVELOPMENTAL CELL, 2004, 6 (05) :661-672
[43]  
Ohta T, 2001, CANCER RES, V61, P1347
[44]   Skp2 protein expression in soft tissue sarcomas [J].
Oliveira, AM ;
Okuno, SH ;
Nascimento, AG ;
Lloyd, RV .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (04) :722-727
[45]   Ubiquitin: structures, functions, mechanisms [J].
Pickart, CM ;
Eddins, MJ .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1695 (1-3) :55-72
[46]  
QIN XQ, 1995, MOL CELL BIOL, V15, P742
[47]   E2F integrates cell cycle progression with DNA repair, replication, and G2/M checkpoints [J].
Ren, B ;
Cam, H ;
Takahashi, Y ;
Volkert, T ;
Terragni, J ;
Young, RA ;
Dynlacht, BD .
GENES & DEVELOPMENT, 2002, 16 (02) :245-256
[48]   Active repression and E2F inhibition by pRB are biochemically distinguishable [J].
Ross, JF ;
Näär, A ;
Cam, H ;
Gregory, R ;
Dynlacht, BD .
GENES & DEVELOPMENT, 2001, 15 (04) :392-397
[49]   Down-regulation of c-myc and Cyclin D1 genes by antisense oligodeoxy nucleotides inhibits the expression of E2F1 and in vitro growth of HepG2 and Morris 5123 liver cancer cells [J].
Simile, MM ;
De Miglio, MR ;
Muroni, MR ;
Frau, M ;
Asara, G ;
Serra, S ;
Muntoni, MD ;
Seddaiu, MA ;
Daino, L ;
Feo, F ;
Pascale, RM .
CARCINOGENESIS, 2004, 25 (03) :333-341
[50]  
Smith EJ, 1996, MOL CELL BIOL, V16, P6965