Anazodo M I, Wainberg M A, Friesen A D, Wright J A
Manitoba Institute of Cell Biology, University of Manitoba, Winnipeg, Canada.
Leukemia. 1995 Oct;9 Suppl 1:S86-8.
We have employed a cos-like monkey kidney cell line (B4.14) transfected with plasmids pCMVgag-pol-rre-r (containing the HIV gag and pol genes) and pCMVrev (containing the HIV rev gene), as a model to investigate whether antisense constructs could interfere with specific HIV gene and protein expression. We utilized an antisense construct (GP12A) directed against a non-regulatory region of the HIV genome, to transfect cells that expressed the above-mentioned HIV genes. Our results show that GP12A was able to attenuate levels of relevant HIV mRNA and gag proteins in the absence of cytotoxic effects.
我们使用了一种经质粒pCMVgag-pol-rre-r(包含HIV gag和pol基因)和pCMVrev(包含HIV rev基因)转染的类COS猴肾细胞系(B4.14),作为研究反义构建体是否会干扰特定HIV基因和蛋白质表达的模型。我们利用一种针对HIV基因组非调控区域的反义构建体(GP12A),转染表达上述HIV基因的细胞。我们的结果表明,在没有细胞毒性作用的情况下,GP12A能够降低相关HIV mRNA和gag蛋白的水平。