Xing Z, Mahadeviah S, Whitton J L
Department of Neuropharmacology, Scripps Research Institute, La Jolla, CA 92037, USA.
Antisense Res Dev. 1995 Fall;5(3):203-12. doi: 10.1089/ard.1995.5.203.
Ribozymes catalytically cleave substrate RNA molecules in a sequence-specific manner. Engineered ribozymes can be developed and introduced into tissue culture cells to regulate gene expression and to inhibit viral replication. We have previously reported on the construction of cell lines that constitutively express a single antiviral ribozyme embedded in a lengthy RNA transcript. These cells exhibited a marked reduction in their ability to support viral infection. Here we report the construction of RNA molecules that contain one or two antiviral ribozymes, each specific for a different cleavage site on the genome of the target virus, lymphocytic choriomeningitis virus (LCMV), and each contained in a self-cleavage cassette comprising cis-acting ribozymes designed to release the antiviral molecules from the transcript. In vitro studies showed that both antiviral ribozymes were released properly from the RNAs following cleavage by the flanking ribozymes and that these released ribozymes functioned as expected in cleaving the target virus RNA. These self-cleaving cassettes have been clones into a retroviral vector downstream of, but in the same transcript as, the chloramphenicol acetyltransferase (CAT) gene. Thus, we hoped to employ CAT as a surrogate marker of ribozyme transcription. Stably transformed cell lines were established. Cleavage by the cis-acting ribozymes was incomplete, as assessed by Northern blot analysis and by the ability of transformed cells to produce infectious retroviral particles. Nevertheless, the antiviral ribozyme sequences exerted effects in tissue culture. LCMV RNA levels in ribozyme-expressing cells were suppressed, and infectious virus yields were decreased by up to 95% compared with normal cells and with cells expressing inverted ribozymes. The antiviral effects correlated with CAT levels, but there was no significant difference between cell lines expressing a single ribozymes and those expressing two.
核酶以序列特异性方式催化切割底物RNA分子。可以开发工程化核酶并将其引入组织培养细胞中,以调节基因表达并抑制病毒复制。我们之前报道过构建组成型表达嵌入长RNA转录本中的单一抗病毒核酶的细胞系。这些细胞支持病毒感染的能力显著降低。在此,我们报道构建包含一个或两个抗病毒核酶的RNA分子,每个核酶对目标病毒淋巴细胞性脉络丛脑膜炎病毒(LCMV)基因组上的不同切割位点具有特异性,并且每个核酶都包含在一个自我切割盒中,该盒包含设计用于从转录本中释放抗病毒分子的顺式作用核酶。体外研究表明,侧翼核酶切割后,两种抗病毒核酶均能从RNA中正确释放,并且这些释放的核酶在切割目标病毒RNA时按预期发挥作用。这些自我切割盒已被克隆到逆转录病毒载体中,位于氯霉素乙酰转移酶(CAT)基因下游,但在同一转录本中。因此,我们希望利用CAT作为核酶转录的替代标志物。建立了稳定转化的细胞系。通过Northern印迹分析以及转化细胞产生传染性逆转录病毒颗粒的能力评估,顺式作用核酶的切割不完全。然而,抗病毒核酶序列在组织培养中发挥了作用。与正常细胞和表达反向核酶的细胞相比,表达核酶的细胞中LCMV RNA水平受到抑制,传染性病毒产量降低了95%。抗病毒作用与CAT水平相关,但表达单一核酶的细胞系与表达两个核酶的细胞系之间没有显著差异。