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猿猴病毒40(SV40)DNA合成的起始并非复制起点所特有。

The initiation of SV40 DNA synthesis is not unique to the replication origin.

作者信息

Martin R G, Setlow V P

出版信息

Cell. 1980 Jun;20(2):381-91. doi: 10.1016/0092-8674(80)90624-8.

Abstract

Replicative intermediates of SV40 were isolated, digested with the restriction endonuclease Bgl I and examined by electron microscopy. Over 98% of the replicative intermediates isolated following infection with wild-type virions at 33 degrees, 37 degrees or 40 degrees C or with tsA209 at 33 degrees C had initiated replication about 35 nucleotides to one side of the Bgl I site. Approximately 1% of the molecules had initiated replication about 2400 nucleotides from the Bgl I site. The remaining molecules may have initiated at other sites. When tsA209 virion-infected cultures were shifted to 40.5 degrees C for 90 min, the relative rate of thymidine incorporation into superhelical viral DNA dropped by more than 97%. The remaining incorporation was not due to "leakiness." The label incorporated into mature superhelical molecules during brief pulses was not preferentially incorporated near the terminus of replication as it was at 33 degrees C. Approximately 33% of the incorporated label represented repair synthesis. Electron microscopy revealed that half of the replicative intermediates formed under these conditions appear to have been initiated randomly around the SV40 genome. Rolling circle molecules contaminated all the preparations of replicative intermediates.

摘要

分离出SV40的复制中间体,用限制性内切酶Bgl I消化,然后通过电子显微镜检查。在33℃、37℃或40℃用野生型病毒粒子感染后,或在33℃用tsA209感染后分离得到的复制中间体中,超过98%在Bgl I位点一侧约35个核苷酸处开始复制。约1%的分子在距Bgl I位点约2400个核苷酸处开始复制。其余分子可能在其他位点开始复制。当用tsA209病毒粒子感染的培养物转移到40.5℃90分钟时,胸苷掺入超螺旋病毒DNA的相对速率下降超过97%。剩余的掺入并非由于“渗漏”。在短暂脉冲期间掺入成熟超螺旋分子中的标记,不像在33℃时那样优先掺入复制末端附近。约33%的掺入标记代表修复合成。电子显微镜显示,在这些条件下形成的复制中间体中有一半似乎是在SV40基因组周围随机起始的。滚环分子污染了所有复制中间体的制备物。

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