Kholodkov O A, Fodor I I
Vestn Ross Akad Med Nauk. 1992(9-10):52-5.
The transient expression of the HIV-1 gag genes and a HIV-1 ++trans-activator protein (tat)-encoded was made in cultured CV-1 cells. In recombinant plasmids, the gag gene was under the control of HIV-1 ++trans-activator sequence (tar) and the tat gene was under the control of a 7.5-kd vaccinia promoter. Transactivation of gag gene expression, which was stimulated by a tat gene expression product, was observed in the presence of wild vaccinia virus. The transaction was immunologically evaluated from the binding to monoclonal anti-p17 and anti-p24 antibodies. The findings lead to the discussion whether the regulatory proteins of HIV-1 can express in vaccinia virus vectors.
在培养的CV-1细胞中实现了HIV-1 gag基因和一种HIV-1反式激活蛋白(tat)编码基因的瞬时表达。在重组质粒中,gag基因受HIV-1反式激活序列(tar)控制,tat基因受7.5-kd痘苗启动子控制。在野生痘苗病毒存在的情况下,观察到由tat基因表达产物刺激的gag基因表达的反式激活。通过与单克隆抗p17和抗p24抗体的结合对这种反式激活进行了免疫学评估。这些发现引发了关于HIV-1的调节蛋白是否能在痘苗病毒载体中表达的讨论。