Hamaguchi M, Nishikawa K, Toyoda T, Yoshida T, Hanaichi T, Nagai Y
Virology. 1985 Dec;147(2):295-308. doi: 10.1016/0042-6822(85)90132-1.
The transcriptive complex, the nucleocapsid with the viral RNA-synthesizing activity, of Newcastle disease virus (NDV) contains three protein components, the major structural subunit (NP) and two associated proteins (P and L) involved in the RNA synthesis. We studied the pathway of these proteins from synthesis to assembly into the complex by pulse-chase labeling of infected cells followed by detergent extraction of the cells to separate soluble and cytoskeletal fractions. Most molecules of NP and P (and probably L) became associated with the cytoskeletal framework immediately after their synthesis. Most of the remaining molecules were initially found in the soluble fraction, but joined the cytoskeletal framework within several minutes. Once attached, none of the proteins left the cytoskeleton, and it was here that they assembled with 50 S viral RNA into nucleocapsids. The nucleocapsids thus formed remained bound to the cytoskeletal framework and were found by in situ autoradiography to exhibit viral RNA synthesis on the framework. These results suggested that the cytoskeletal framework could actively participate in the structural and functional assembly of NDV transcriptive complex.
新城疫病毒(NDV)具有病毒RNA合成活性的转录复合体,即核衣壳,包含三种蛋白质成分,主要结构亚基(NP)以及参与RNA合成的两种相关蛋白(P和L)。我们通过对感染细胞进行脉冲追踪标记,随后用去污剂提取细胞以分离可溶性和细胞骨架部分,研究了这些蛋白质从合成到组装入复合体的途径。NP和P的大多数分子(可能还有L)在合成后立即与细胞骨架框架结合。其余大多数分子最初存在于可溶性部分,但在几分钟内就加入了细胞骨架框架。一旦附着,这些蛋白质都不会离开细胞骨架,正是在这里它们与50S病毒RNA组装成核衣壳。如此形成的核衣壳仍与细胞骨架框架结合,并且通过原位放射自显影发现在该框架上表现出病毒RNA合成。这些结果表明,细胞骨架框架可以积极参与新城疫病毒转录复合体的结构和功能组装。