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在大肠杆菌dnaA突变体中积累起始潜能表达期间DNA复制的不连续性。

Discontinuity in DNA replication during expression of accumulated initiation potential in dnaA mutants of Escherichia coli.

作者信息

Helmstetter C E, Krajewski C A, Leonard A C, Weinberger M

出版信息

J Bacteriol. 1986 Feb;165(2):631-7. doi: 10.1128/jb.165.2.631-637.1986.

Abstract

Potential for initiation of chromosome replication present in temperature-sensitive, initiation-defective dnaA5 mutants of Escherichia coli B/r incubated at nonpermissive temperature was expressed by shifting to a more permissive temperature (25 degrees C). Upon expression of initiation potential, the rate of [3H]thymidine incorporation varied in a bimodal fashion, i.e., there was an initial burst of incorporation, which lasted 10 to 20 min, then a sudden decrease in incorporation, and finally a second rapid increase in incorporation. Analyses of this incorporation pattern indicated that a round of replication initiated upon expression of initiation potential, but DNA polymerization stopped after replication of 5 to 10% of the chromosome. This round of replication appeared to resume about 30 min later coincident with initiation of a second round of replication. The second initiation was unusually sensitive to low concentrations of novobiocin (ca. 1 microgram/ml) when this inhibitor was added in the presence of chloramphenicol. In the absence of chloramphenicol, novobiocin at this concentration had no detectable effect on DNA replication. It is suggested that cis-acting inhibition, attributable to an attempted second initiation immediately after the first, caused the first round to stall until both it and the second round could resume simultaneously. This DNA replication inhibition, probably caused by overinitiation, could be a consequence of restraints on replication in the vicinity of oriC, possibly topological in nature, which limit the minimum interinitiation interval in E. coli.

摘要

将大肠杆菌B/r的温度敏感型、起始缺陷型dnaA5突变体在非允许温度下培养时所具有的启动染色体复制的潜力,通过转移到更宽松的温度(25摄氏度)来表达。在启动潜力表达后,[3H]胸苷掺入率呈双峰变化,即最初有一个持续10到20分钟的掺入高峰,然后掺入突然下降,最后掺入再次快速增加。对这种掺入模式的分析表明,一轮复制在启动潜力表达时开始,但DNA聚合在染色体复制5%到10%后停止。这一轮复制似乎在大约30分钟后恢复,与第二轮复制的启动同时发生。当在氯霉素存在的情况下加入这种抑制剂时,第二次起始对低浓度的新生霉素(约1微克/毫升)异常敏感。在没有氯霉素的情况下,这个浓度的新生霉素对DNA复制没有可检测到的影响。有人提出,由于第一次启动后立即尝试第二次启动导致的顺式作用抑制,使得第一轮复制停滞,直到第一轮和第二轮复制能够同时恢复。这种可能由过度起始引起的DNA复制抑制,可能是oriC附近复制限制的结果,可能本质上是拓扑学上的,这限制了大肠杆菌中的最小起始间隔。

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