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在SV40 DNA复制过程中,优选的DNA位点参与DNA合成的起始和终止。

Preferred DNA sites are involved in the arrest and initiation of DNA synthesis during replication of SV40 DNA.

作者信息

Tapper D P, DePamphilis M L

出版信息

Cell. 1980 Nov;22(1 Pt 1):97-108. doi: 10.1016/0092-8674(80)90158-0.

Abstract

Previous analysis of simian virus 40 (SV40) DNA replication revealed a 2-4 fold excess of DNA molecules that were 90 +/- 2% replicated, demonstrating that replication forks accumulate near the termination site. To determine whether replication is arrested at specific DNA sites, forks were located on the SV40 genome by specifically 32P labelling 3' ends of nascent DNA on purified replicating SV40 DNA, isolating the longest 32P-DNA chains, annealing them to SV40 DNA and then digesting them with a restriction endonuclease that cut near the terminatin site. 32P-DNA fragments of several discrete lengths were released, demonstrating that replication forks on native chromosomes were arrested at preferred sites on the DNA. Most forks were arrested when bidirectional DNA replication was 91% completed, and the two forks were separated by about 470 bp of unreplicated DNA centered at the expected termination site. Forks were also arrested at other locations such that the center of the termination region defined by DNA arrest sites varied by +/- 450 bp. Electron microscopic analysis of replicating DNA suggested that such variation may result from asynchronous arrival of some replication forks. Analysis of 5' end-labeled nascent DNA demonstrated that initiation of Okazaki fragments was also promoted at preferred DNA sites (about 100-120 per genome). Thus specific DNA sequences appear to be utilized throughout DNA replication, not just at the origin.

摘要

先前对猴病毒40(SV40)DNA复制的分析表明,已复制90±2%的DNA分子数量多出2至4倍,这表明复制叉在终止位点附近积累。为了确定复制是否在特定的DNA位点停滞,通过对纯化的正在复制的SV40 DNA上新生DNA的3'末端进行特异性32P标记来定位复制叉,分离出最长的32P-DNA链,将它们与SV40 DNA退火,然后用一种在终止位点附近切割的限制性内切酶进行消化。释放出几种不同长度的32P-DNA片段,这表明天然染色体上的复制叉在DNA上的优先位点停滞。当双向DNA复制完成91%时,大多数复制叉停滞,并且两个复制叉被大约470 bp未复制的DNA隔开,该未复制DNA以预期的终止位点为中心。复制叉也在其他位置停滞,使得由DNA停滞位点定义的终止区域的中心变化±450 bp。对正在复制的DNA的电子显微镜分析表明,这种变化可能是由于一些复制叉异步到达所致。对5'末端标记的新生DNA的分析表明,冈崎片段的起始也在优先的DNA位点(每个基因组约100 - 120个)得到促进。因此,特定的DNA序列似乎在整个DNA复制过程中都被利用,而不仅仅是在起始位点。

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