Dixon L K, Koenig I, Hohn T
Gene. 1983 Nov;25(2-3):189-99. doi: 10.1016/s0378-1119(83)80001-8.
A series of insertion mutants of cauliflower mosaic virus (CaMV) DNA has been constructed in vitro. These insertions consist of a short DNA sequence (10 or 22 bp) containing a restriction endonuclease site (SmaI) not represented on the viral DNA. Viral infectivity was analyzed by inoculating plants with the mutated cloned viral DNA and observing symptoms. Insertions within ORFVII, and in one site within the large intergenic region, did not interfere with viral infectivity, whilst insertions within ORFII and at the end of ORFIV retarded the development of viral symptoms. All other insertion mutants analyzed were lethal. CaMV with a deletion of 105 bp within ORFVII was viable. Such viable mutants can be used to construct additional deletions or to insert foreign DNA into the viral genome.
已在体外构建了一系列花椰菜花叶病毒(CaMV)DNA的插入突变体。这些插入片段由一个短DNA序列(10或22 bp)组成,该序列包含一个病毒DNA上不存在的限制性内切酶位点(SmaI)。通过用突变的克隆病毒DNA接种植物并观察症状来分析病毒感染性。ORFVII内以及大基因间隔区内一个位点的插入不影响病毒感染性,而ORFII内和ORFIV末端的插入则延缓了病毒症状的发展。分析的所有其他插入突变体都是致死的。ORFVII内缺失105 bp的CaMV是有活力的。这种有活力的突变体可用于构建额外的缺失或将外源DNA插入病毒基因组。