Dubielzig R, King J A, Weger S, Kern A, Kleinschmidt J A
Deutsches Krebsforschungszentrum, Forschungsschwerpunkt Angewandte Tumorvirologie, D-69120 Heidelberg, Germany.
J Virol. 1999 Nov;73(11):8989-98. doi: 10.1128/JVI.73.11.8989-8998.1999.
The nonstructural adeno-associated virus type 2 Rep proteins are known to control viral replication and thus provide the single-stranded DNA genomes required for packaging into preformed capsids. In addition, complexes between Rep proteins and capsids have previously been observed in the course of productive infections. Such complexes have been interpreted as genome-linked Rep molecules associated with the capsid upon successful DNA encapsidation. Here we demonstrate via coimmunoprecipitation, cosedimentation, and yeast two-hybrid analyses that the Rep-VP association also occurs in the absence of packageable genomes, suggesting that such complexes could be involved in the preparation of empty capsids for subsequent encapsidation steps. The Rep domain responsible for the observed Rep-VP interactions is situated within amino acids 322 to 482. In the presence of all Rep proteins, Rep52 and, to a lesser extent, Rep78 are most abundantly recovered with capsids, whereas Rep68 and Rep40 vary in association depending on their expression levels. Rep78 and Rep52 are bound to capsids to roughly the same extent as the minor capsid protein VP2. Complexes of Rep78 and Rep52 with capsids differ in their respective detergent stabilities, indicating that they result from different types of interactions. Rep-VP interaction studies suggest that Rep proteins become stably associated with the capsid during the assembly process. Rep-capsid complexes can reach even higher complexity through additional Rep-Rep interactions, which are particularly detergent labile. Coimmunoprecipitation and yeast two-hybrid data demonstrate the interaction of Rep78 with Rep68, of Rep68 with Rep52, and weak interactions of Rep40 with Rep52 and Rep78. We propose that the large complexes arising from these interactions represent intermediates in the DNA packaging pathway.
已知2型腺相关病毒的非结构Rep蛋白可控制病毒复制,从而提供包装到预先形成的衣壳中所需的单链DNA基因组。此外,在生产性感染过程中,以前曾观察到Rep蛋白与衣壳之间形成复合物。这种复合物被解释为在DNA成功衣壳化后与衣壳相关的基因组连接Rep分子。在这里,我们通过共免疫沉淀、共沉降和酵母双杂交分析证明,在不存在可包装基因组的情况下,Rep与VP也会发生相互作用,这表明这种复合物可能参与空衣壳的制备,以便进行后续的衣壳化步骤。负责观察到的Rep-VP相互作用的Rep结构域位于氨基酸322至482之间。在所有Rep蛋白存在的情况下,Rep52以及程度稍低的Rep78与衣壳的结合最为丰富,而Rep68和Rep40的结合则根据其表达水平而有所不同。Rep78和Rep52与衣壳的结合程度与次要衣壳蛋白VP2大致相同。Rep78和Rep52与衣壳的复合物在各自的去污剂稳定性方面有所不同,这表明它们是由不同类型的相互作用导致的。Rep-VP相互作用研究表明,Rep蛋白在组装过程中与衣壳稳定结合。Rep-衣壳复合物可通过额外的Rep-Rep相互作用达到更高的复杂性,这些相互作用对去污剂特别敏感。共免疫沉淀和酵母双杂交数据证明了Rep78与Rep68、Rep68与Rep52之间的相互作用,以及Rep40与Rep52和Rep78之间的弱相互作用。我们提出,由这些相互作用产生的大复合物代表DNA包装途径中的中间体。