Zakharchuk A N, Doronin K K, Karpov V A, Krougliak V A, Naroditsky B S
Institute of Agricultural Biotechnology, Moscow, Russian Federation.
Gene. 1995 Aug 19;161(2):189-93. doi: 10.1016/0378-1119(95)00251-z.
A new system for hammerhead ribozyme (Rz) expression was examined in which fowl adenovirus type 1 (CELO) virus-associated RNA (CELO VA RNA) was used as a vector for the incorporation of Rz to target the mRNA of secreted alkaline phosphatase (SEAP) both in vitro and in vivo. The Rz gene was integrated into the CELO VA RNA between the internal promoter boxes A and B; apparently this did not interfere with its transcription. Rz integrated into CELO VA RNA and, lacking the viral sequences, exhibited the same activity in vitro, Consequently, CELO VA RNA sequences did not inhibit the integrated Rz activity in vitro. In vivo experiments were carried out with human 293 cells by co-transfection with plasmids containing Rz and SEAP. Inhibition of enzyme activity was 50% in 48 h. We conclude that CELO VA RNA may be used for effective expression of hammerhead Rz.
研究了一种新的锤头状核酶(Rz)表达系统,其中1型禽腺病毒(CELO)病毒相关RNA(CELO VA RNA)被用作载体,用于整合Rz以在体外和体内靶向分泌性碱性磷酸酶(SEAP)的mRNA。Rz基因被整合到CELO VA RNA内部启动子盒A和B之间;显然这并不干扰其转录。整合到CELO VA RNA中的Rz,由于缺乏病毒序列,在体外表现出相同的活性。因此,CELO VA RNA序列在体外不抑制整合的Rz活性。通过与含有Rz和SEAP的质粒共转染,对人293细胞进行了体内实验。48小时内酶活性的抑制率为50%。我们得出结论,CELO VA RNA可用于锤头状Rz的有效表达。