Oncogenic potential of the DNA replication licensing protein CDT1

被引:105
|
作者
Arentson, E
Faloon, P
Seo, J
Moon, E
Studts, JM
Fremont, DH
Choi, KH
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Ajou Univ, Dept Biol Sci, Suwon 441749, South Korea
关键词
CDT1; retroviral insertional activation; oncogene;
D O I
10.1038/sj.onc.1205175
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 expression of a gene, designated as Retroviral insertion site (Ris)2, was activated by retroviral DNA integration in an immortalized primitive erythroid cell line, EB-PE. Ris2 was also expressed at high levels in all human tumor cell lines analysed. Consistently, NIH3T3 fibroblasts overexpressing Ris2 formed tumors in Rag2(-/-) mice when injected subcutaneously. The putative RIS2 protein shows a high sequence similarity to Xenopus CDT1, Drosophila DUP, and human CDT1, a newly identified DNA replication licensing protein, suggesting that Ris2 is a mouse homologue of CDT1. Cells overexpressing Ris2/Cdt1 exhibited a quicker entry into S phase when released from serum starvation compared to controls. Our results suggest that CDT1, an essential licensing protein for DNA replication, can function as an oncogene in mammals.
引用
收藏
页码:1150 / 1158
页数:9
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