Wodrich Harald, Guan Tinglu, Cingolani Gino, Von Seggern Dan, Nemerow Glen, Gerace Larry
Department of Cell Biology, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, CA 92037, USA.
EMBO J. 2003 Dec 1;22(23):6245-55. doi: 10.1093/emboj/cdg614.
Replication and assembly of adenovirus occurs in the nucleus of infected cells, requiring the nuclear import of all viral structural proteins. In this report we show that nuclear import of the major capsid protein, hexon, is mediated by protein VI, a structural protein located underneath the 12 vertices of the adenoviral capsid. Our data indicate that protein VI shuttles between the nucleus and the cytoplasm and that it links hexon to the nuclear import machinery via an importin alpha/beta-dependent mechanism. Key nuclear import and export signals of protein VI are located in a short C-terminal segment, which is proteolytically removed during virus maturation. The removal of these C-terminal transport signals appears to trigger a functional transition in protein VI, from a role in supporting hexon nuclear import to a structural role in virus assembly.
腺病毒的复制和组装发生在受感染细胞的细胞核中,这需要所有病毒结构蛋白进行核输入。在本报告中,我们表明主要衣壳蛋白六邻体的核输入是由蛋白VI介导的,蛋白VI是一种位于腺病毒衣壳12个顶点下方的结构蛋白。我们的数据表明,蛋白VI在细胞核和细胞质之间穿梭,并且它通过一种依赖于输入蛋白α/β的机制将六邻体与核输入机制联系起来。蛋白VI的关键核输入和输出信号位于一个短的C末端片段中,该片段在病毒成熟过程中被蛋白酶水解去除。这些C末端转运信号的去除似乎触发了蛋白VI的功能转变,从支持六邻体核输入的作用转变为病毒组装中的结构作用。