Melucci-Vigo G, Magnusson G, Risuleo G
Dipartimento di Genetica e Biologia Molecolare, Università di Roma La Sapienza, Italy.
Virus Genes. 1994 Mar;8(2):137-41. doi: 10.1007/BF01703070.
We have constructed mouse polyomavirus mutants with deletions or insertions in the late region. These viral constructs exhibit two different phenotypes, characterized by a differential replication ability. The first type shows a twofold higher level of DNA synthesis with respect to wild type, while mutants of the second type are virtually unable to replicate. In this paper we investigate the replicative behavior of the first class of mutants, which expresses defective viral coat proteins. Our data raise the possibility that, of the three late gene viral products, VP2 is involved in the formation of an encapsidation intermediate that, in an indirect fashion, affects the rate of viral DNA synthesis.
我们构建了在晚期区域有缺失或插入的小鼠多瘤病毒突变体。这些病毒构建体表现出两种不同的表型,其特征在于具有不同的复制能力。第一类相对于野生型显示出两倍高的DNA合成水平,而第二类突变体实际上无法复制。在本文中,我们研究了第一类表达缺陷病毒衣壳蛋白的突变体的复制行为。我们的数据提出了一种可能性,即在三种晚期基因病毒产物中,VP2参与了衣壳化中间体的形成,该中间体以间接方式影响病毒DNA合成的速率。