Activation of cyclin A gene expression by the cyclin encoded by human herpesvirus-8

被引:18
作者
Duro, D
Schulze, A
Vogt, B
Bartek, J
Mittnacht, S
Jansen-Dürr, P
机构
[1] Deutsch Krebsforschungszentrum, Forschungsschwerpunkt Angew Tumorvirol, Abt 620, D-69120 Heidelberg, Germany
[2] Danish Canc Soc, Div Canc Biol, DK-21000 Copenhagen, Denmark
[3] Inst Canc Res, Ctr Mol & Cell Biol, Chester Beatty Labs, London SW3 6JB, England
关键词
D O I
10.1099/0022-1317-80-3-549
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Human herpesvirus-8 (HHV-8), also known as Kaposi's sarcoma-associated herpesvirus, encodes a protein, referred to as HHV8-Vcyc, with sequence similarity to human G1 cyclins, in particular of the D type. HHV8-Vcyc is expressed in Kaposi's sarcoma and functional analysis suggests that it can activate cyclin-dependent kinases (cdk) and thereby trigger inactivation of the retinoblastoma protein (pRb), indicating that HHV8-Vcyc may contribute to the oncogenic potential of HHV-8, We show here that HHV8-Vcyc can activate transcription of the human cyclin A gene in quiescent cells, a property shared with known transforming oncogenes, Transcriptional activation by HHV8-Vcyc depends on an E2F-binding site in the cyclin A promoter, and cdk6 kinase activity is required, The ability of HHV8-Vcyc to activate cyclin A gene expression is shared by D-type cyclins and cyclin E. Unlike D-type cyclins, HHV8-Vcyc is unable to trigger phosphorylation of the pRb-related protein p107 and fails to induce dissociation of p107 from E2F, Unlike cyclin E, HHV8-Vcyc fails to interact physically with E2F complexes on the cyclin A promoter, These results provide additional evidence for the notion that the HHV-8-encoded cyclin differs in several properties from cellular G1 cyclins.
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页码:549 / 555
页数:7
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