Corsini J, Carlson J O, Maxwell F, Maxwell I H
Department of Microbiology, Colorado State University, Ft. Collins 80523.
J Virol. 1995 Apr;69(4):2692-6. doi: 10.1128/JVI.69.4.2692-2696.1995.
LuIII is an autonomous parvovirus which encapsidates either strand of its genome with similar efficiency in NB324K cells. Two parvoviruses closely related to LuIII, minute virus of mice (MVM) and H-1 virus, encapsidate primarily the minus strand of their genome when grown in the same cell type. It has been postulated that an AT-rich region unique to LuIII is responsible for symmetric encapsidation of plus- and minus-strand genomes by LuIII. To address this hypothesis, recombinant LuIII-luciferase genomes containing or lacking the AT-rich sequence (AT) were packaged into LuIII virions. Hybridization of strand-specific probes to DNA from these virions revealed that either strand of the genome was packaged regardless of the presence of AT. In addition, encapsidation of both strands of the AT+ LuIII-luciferase genome into MVM and H-1 virions was observed, suggesting that MVM and H-1 viral proteins are not responsible for the minus-strand packaging bias of these two viruses. Alignment of the published LuIII and MVMp sequences shows that AT exists as an insertion into an element that, in MVM, binds cellular proteins. We suggest that in LuIII, AT disrupts binding of these cellular proteins, allowing encapsidation of either strand.
LuIII是一种自主细小病毒,在NB324K细胞中,它以相似的效率将其基因组的两条链包装起来。两种与LuIII密切相关的细小病毒,小鼠微小病毒(MVM)和H-1病毒,在相同细胞类型中生长时,主要将其基因组的负链包装起来。据推测,LuIII特有的富含AT的区域负责LuIII对正链和负链基因组的对称包装。为了验证这一假设,将含有或缺乏富含AT序列(AT)的重组LuIII-荧光素酶基因组包装到LuIII病毒粒子中。用链特异性探针与这些病毒粒子的DNA杂交,结果显示,无论是否存在AT,基因组的任何一条链都能被包装。此外,还观察到AT+ LuIII-荧光素酶基因组的两条链都被包装到MVM和H-1病毒粒子中,这表明MVM和H-1病毒蛋白与这两种病毒的负链包装偏好无关。已发表的LuIII和MVMp序列比对显示,AT作为一个插入元件存在,在MVM中,该元件能结合细胞蛋白。我们认为,在LuIII中,AT会破坏这些细胞蛋白的结合,从而使任何一条链都能被包装。