Cantor G H, Stone D M, McElwain T F, Palmer G H
Department of Veterinary Microbiology and Pathology, Washington State University, Pullman 99164-7040, USA.
Antisense Nucleic Acid Drug Dev. 1996 Winter;6(4):301-4. doi: 10.1089/oli.1.1996.6.301.
Despite the theoretical attraction of ribozymes, which cleave their target RNA, as compared with antisense RNA, which only blocks translation, few studies have assessed the relative efficacy of ribozymes and antisense RNA directed against the identical target sequence. Previously, we described the efficacy of a hammerhead ribozyme targeted against rex/tax, a regulatory gene of bovine leukemia virus (BLV). In this study, we asked whether antisense RNA targeted against the same site would also be efficacious. BLV-infected bat lung cells were transfected with an antisense RNA-encoding plasmid under the control of sarcoma virus (RSV) promoter, and stable cell lines were selected. No inhibition of viral p24 expression was demonstrated in seven cell lines transfected with the antisense RNA targeted at the same site as the ribozyme or in three cell lines transfected with an antisense sequence targeted against the tax 5' initiation codon. Although in previous experiments antisense DNA oligonucleotides inhibited Tax expression in vitro, stably transfected plasmids encoding antisense RNA of the same sequence did not inhibit viral expression in BLV-infected cells in this study. These results suggest that in persistently infected cells producing high levels of BLV, the ribozyme is more effective than antisense RNA directed at rex/tax transcripts.
与仅阻断翻译的反义RNA相比,核酶可切割其靶RNA,尽管从理论上看核酶很有吸引力,但很少有研究评估针对相同靶序列的核酶和反义RNA的相对效力。此前,我们描述了一种针对牛白血病病毒(BLV)调控基因rex/tax的锤头状核酶的效力。在本研究中,我们探究了针对相同位点的反义RNA是否也有效。用肉瘤病毒(RSV)启动子控制下的编码反义RNA的质粒转染感染了BLV的蝙蝠肺细胞,并筛选出稳定的细胞系。在转染了与核酶靶向相同位点的反义RNA的7个细胞系中,以及在转染了针对tax 5'起始密码子的反义序列的3个细胞系中,均未显示出对病毒p24表达的抑制作用。尽管在先前的实验中反义DNA寡核苷酸在体外抑制了Tax表达,但在本研究中,编码相同序列反义RNA的稳定转染质粒并未抑制BLV感染细胞中的病毒表达。这些结果表明,在持续产生高水平BLV的感染细胞中,核酶比针对rex/tax转录本的反义RNA更有效。