Salvino R, Skiadopoulos M, Faust E A, Tam P, Shade R O, Astell C R
Department of Biochemistry, Dalhousie University, Halifax, Nova Scotia, Canada.
J Virol. 1991 Mar;65(3):1352-63. doi: 10.1128/JVI.65.3.1352-1363.1991.
Mutations were introduced into plasmid pMM984, a full-length infectious clone of the fibrotropic strain of minute virus of mice, to identify cis-acting genetic elements required for the excision and replication of the viral genome. The replicative capacity of these mutants was measured directly, using an in vivo transient DNA replication assay following transfection of plasmids into murine A9 cells and primate COS-7 cells. Experiments with subgenomic constructs indicated that both viral termini must be present on the same DNA molecule for replication to occur and that the viral nonstructural protein NS-1 must be provided in trans. The necessary sequences were located within 1,084 and 807 nucleotides of the 3' and 5' ends of the minute virus of mice genome, respectively. The inhibitory effect of deletions within the 206-bp 5'-terminal palindrome demonstrated that these sequences comprise a cis-acting genetic element that is absolutely essential for the excision and replication of viral DNA. The results further indicated a requirement for a stem-plus-arms T structure as well as for the formation of a simple hairpin. In addition, the removal of one copy of a tandemly arranged 65-bp repeat found 94 nucleotides inboard of the 5'-terminal palindrome inhibited viral DNA replication in cis by 10- and just greater than 100-fold in A9 and COS-7 cells, respectively. The latter results define a novel genetic element within the 65-bp repeated sequence, distinct from the terminal palindrome, that is capable of regulating minute virus of mice DNA replication in a species-specific manner.
将突变引入质粒pMM984(小鼠微小病毒纤维嗜性毒株的全长感染性克隆),以鉴定病毒基因组切除和复制所需的顺式作用遗传元件。在将质粒转染到小鼠A9细胞和灵长类COS-7细胞后,使用体内瞬时DNA复制测定法直接测量这些突变体的复制能力。亚基因组构建体实验表明,两个病毒末端必须存在于同一DNA分子上才能发生复制,并且病毒非结构蛋白NS-1必须通过反式提供。必要序列分别位于小鼠微小病毒基因组3'和5'末端的1,084和807个核苷酸内。206 bp 5'末端回文序列内缺失的抑制作用表明,这些序列构成了一个顺式作用遗传元件,对于病毒DNA的切除和复制绝对必要。结果进一步表明需要一个茎加臂T结构以及形成一个简单的发夹结构。此外,去除位于5'末端回文序列内侧94个核苷酸处串联排列的65 bp重复序列的一个拷贝,分别在A9和COS-7细胞中顺式抑制病毒DNA复制10倍和大于100倍。后一结果在65 bp重复序列内定义了一个新的遗传元件,与末端回文序列不同,它能够以物种特异性方式调节小鼠微小病毒DNA复制。