Jasny B R, Cohen J E, Tamm I
Chromosoma. 1980;79(2):207-14. doi: 10.1007/BF01175186.
DNA fiber autoradiography was used to analyze the spatial and temporal organization of activated initiation sites for DNA replication in mouse L929 cells infected with reovirus type 3 (Dearing strain) and in uninfected control cells. Cells were labeled for 10 min with 3H-thymidine at high specific activity followed by 3 h of low specific activity labeling. Reovirus infection causes no change in the rate of replication fork progression, but increases both the mean distance between activated initiation sites by approximately 30% and the nonrandomness in the spatial distribution of the sites along the DNA fibers. Significant synchronization of initiation in adjacent activated sites was detected on DNA fibers from uninfected cells and from reovirus-infected cells. The mean relative initiation time for pairs of initiation events which had occurred prior to high specific activity labeling did not differ significantly between the infected and uninfected cells. The data are consistent with the interpretation that reovirus infection shuts off initiation sites in a coordinated fashion, possibly by preventing activation of entire clusters of potential initiation sites.
采用DNA纤维放射自显影技术,分析感染3型呼肠孤病毒(迪尔林株)的小鼠L929细胞和未感染的对照细胞中DNA复制起始位点的时空组织。先用高比活度的³H-胸腺嘧啶核苷标记细胞10分钟,然后用低比活度标记3小时。呼肠孤病毒感染不会改变复制叉推进速率,但会使激活的起始位点之间的平均距离增加约30%,同时这些位点沿DNA纤维的空间分布的非随机性也增加。在未感染细胞和呼肠孤病毒感染细胞的DNA纤维上均检测到相邻激活位点起始的显著同步性。在高比活度标记之前发生的起始事件对的平均相对起始时间,在感染细胞和未感染细胞之间没有显著差异。这些数据符合这样的解释:呼肠孤病毒感染以协调的方式关闭起始位点,可能是通过阻止潜在起始位点的整个簇的激活。