Korn R, Horwitz M S
Virology. 1986 Apr 30;150(2):342-51. doi: 10.1016/0042-6822(86)90299-0.
The effects of the adenovirus type 2 (Ad2) structural proteins on Ad DNA synthesis in vitro have been examined. Both of the viral core proteins, polypeptides V and VII were shown to inhibit Ad2 DNA synthesis in vitro; however, only the major core protein, polypeptide VII, inhibited DNA synthesis at a ratio of protein to DNA proportional to the number of polypeptide VII molecules associated with the Ad2 DNA in the mature virion. In addition, fractions containing the precursor to polypeptide VII, pVII, were capable of inhibiting Ad2 DNA replication in vitro to the same extent as polypeptide VII. Purified polypeptide VII bound to double-stranded DNA with no apparent sequence specificity. In addition, polypeptide VII protected Ad2 DNA from digestion with micrococcal nuclease. The binding of polypeptide VII was probably responsible for the inhibition of Ad2 DNA synthesis in vitro by virtue of rendering the DNA inaccessible to viral replication proteins. These results suggest that the core proteins must be removed from the Ad2 genome before the template can function in genome replication and that assembly of pVII on Ad2 DNA can terminate the replication process.
已对2型腺病毒(Ad2)结构蛋白在体外对Ad DNA合成的影响进行了研究。两种病毒核心蛋白,即多肽V和VII,均显示在体外抑制Ad2 DNA合成;然而,只有主要核心蛋白多肽VII以与成熟病毒体中与Ad2 DNA相关的多肽VII分子数量成比例的蛋白质与DNA比例抑制DNA合成。此外,含有多肽VII前体pVII的组分在体外抑制Ad2 DNA复制的程度与多肽VII相同。纯化的多肽VII与双链DNA结合,没有明显的序列特异性。此外,多肽VII保护Ad2 DNA不被微球菌核酸酶消化。多肽VII的结合可能由于使DNA无法被病毒复制蛋白接近而导致体外Ad2 DNA合成受到抑制。这些结果表明,在模板能够在基因组复制中发挥作用之前,必须从Ad2基因组中去除核心蛋白,并且pVII在Ad2 DNA上的组装可以终止复制过程。