Etessami P, Saunders K, Watts J, Stanley J
Department of Virus Research, John Innes Institute, John Innes Centre for Plant Science Research, Norwich, U.K.
J Gen Virol. 1991 May;72 ( Pt 5):1005-12. doi: 10.1099/0022-1317-72-5-1005.
We have investigated the ability of African cassava mosaic virus DNA A mutants, containing disrupted complementary-sense genes, to infect Nicotiana benthamiana and to replicate in Nicotiana tabacum protoplasts. Three overlapping open reading frames (ORFs) with the capacity to encode proteins with an Mr greater than 10K (AC1, AC2 and AC3) are highly conserved between geminiviruses that infect dicotyledonous plants and one (AC4) is less well conserved. Of these, only AC1 is a prerequisite for DNA replication; disruption of this ORF rendered the DNA noninfectious in plants and prevented DNA replication in protoplasts. Disruption of ORF AC2 prevented plant infection but mutants were capable of autonomous replication and replicated DNA B in trans in protoplasts to produce DNA forms that comigrated with wild-type virus DNAs. The AC2 mutant phenotype suggests that the product of this ORF is involved in virus spread within the plant. Mutants in which ORF AC3 had been disrupted retained the ability to replicate and to infect plants systemically although symptom development was delayed and attenuated, and mutant DNA accumulated to much lower levels (10 to 20%) in comparison with wild-type infection. Typical geminate virus particles were observed in extracts of plants infected with ORF AC3 mutants indicating that this gene is not essential for coat protein synthesis or virus assembly but possibly acts by modulating virus levels in infected tissues. Disruption of ORF AC4 had no effect on infectivity or symptom development suggesting that this ORF is maintained only because it overlaps the highly conserved ORF AC1.
我们研究了含有被破坏的互补链基因的非洲木薯花叶病毒DNA A突变体感染本氏烟草并在烟草原生质体中复制的能力。在感染双子叶植物的双生病毒之间,三个能够编码分子量大于10K的蛋白质的重叠开放阅读框(ORF)(AC1、AC2和AC3)高度保守,而其中一个(AC4)的保守性较差。其中,只有AC1是DNA复制的前提条件;该ORF的破坏使DNA在植物中无感染性,并阻止其在原生质体中复制。ORF AC2的破坏阻止了植物感染,但突变体能够自主复制,并在原生质体中反式复制DNA B,以产生与野生型病毒DNA共迁移的DNA形式。AC2突变体表型表明该ORF的产物参与病毒在植物体内的传播。ORF AC3被破坏的突变体仍保留复制和系统性感染植物的能力,尽管症状发展延迟且减弱,与野生型感染相比,突变体DNA积累水平低得多(10%至20%)。在感染ORF AC3突变体的植物提取物中观察到典型的双生病毒颗粒,表明该基因对于外壳蛋白合成或病毒组装不是必需的,但可能通过调节感染组织中的病毒水平发挥作用。ORF AC4的破坏对感染性或症状发展没有影响,这表明该ORF得以保留只是因为它与高度保守的ORF AC1重叠。