c-Myb influences HIV type 1 gene expression and virus production

被引:10
作者
Churchill, MJ
Ramsay, RG
Rhodes, DI
Deacon, NJ
机构
[1] Macfarlane Burnet Ctr Med Res, Natl Ctr HIV Virol Res, AIDS Mol Biol Unit, Fairfield, Vic 3078, Australia
[2] Peter MacCallum Canc Inst, Melbourne, Vic 3002, Australia
关键词
D O I
10.1089/08892220152644188
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
c-Myb is expressed in proliferating T cells. Fifteen c-Myb-binding sites can be identified in the HIV-1 long terminal repeat (LTR), suggesting that c-Myb may regulate HIV-1 gene expression and virus replication. Increasing the cellular levels of c-Myb by transient transfection of CEM cells resulted in a 10- to 20-fold activation of HIV-1 LTR-driven gene expression and mutation of one high-affinity Myb-binding site within the LTR reduced this activation by 60 to 70%. Conversely, inhibition of c-Myb expression in MT-2 cells by treatment with c-myb antisense oligonucleotides decreased HIV-1 replication by 85%, as measured by reverse transcriptase activity and cytopathic effects. The effect of c-myb antisense oligonucleotides on HIV-1 gene expression and virus particle production appeared to be independent of cell proliferation, but dependent on the presence of c-Myb activity mediated through the HIV-1 LTR. These data show that c-myb expression affects HIV-1 replication in CD4(+) T cells.
引用
收藏
页码:1481 / 1488
页数:8
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