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确定的寡聚体SV40 DNA:体细胞中一般重组的灵敏探针。

Defined oligomeric SV40 DNA: a sensitive probe of general recombination in somatic cells.

作者信息

Wake C T, Wilson J H

出版信息

Cell. 1980 Aug;21(1):141-8. doi: 10.1016/0092-8674(80)90121-x.

Abstract

We have constructed well defined oligomeric molecules of simian virus 40 (SV40) DNA as probes for investigating mechanisms by which cultured somatic cells recombine DNA. Restriction enzyme fragments from different temperature-sensitive mutants were joined in a head-to-tail orientation to create partial dimers 1.84 genome lengths in size. These molecules are too large to fit into a viral capsid. Therefore an assay that depends on production of progeny virus after infection with oligomeric DNA is a selective measure of precise conversion of oligomers to monomers. By constructing oligomers from appropriate combinations of temperature-sensitive DNAs, we have been able to study the conversion process in several defined regions of the SV40 genome. Our results indicate that conversion of oligomers to monomers occurs uniformly throughout the genome and is not dependent on normal viral DNA replication. These data indicate that conversion occurs primarily by general, homology-dependent recombination. At least one secondary mechanism that generates a low level of wild-type progeny was also detected. Studies with heteroduplex molecules indicate that repair of mismatched bases may be the secondary mechanism.

摘要

我们构建了明确的猿猴病毒40(SV40)DNA寡聚分子,作为研究培养的体细胞重组DNA机制的探针。来自不同温度敏感突变体的限制性酶切片段以头对尾的方向连接,形成大小为1.84个基因组长度的部分二聚体。这些分子太大,无法装入病毒衣壳。因此,一种依赖于用寡聚DNA感染后产生子代病毒的检测方法,是寡聚体精确转化为单体的选择性测量方法。通过从温度敏感DNA的适当组合构建寡聚体,我们能够研究SV40基因组几个特定区域的转化过程。我们的结果表明,寡聚体向单体的转化在整个基因组中均匀发生,并且不依赖于正常的病毒DNA复制。这些数据表明,转化主要通过一般的、同源依赖性重组发生。还检测到至少一种产生低水平野生型子代的次要机制。对异源双链分子的研究表明,错配碱基的修复可能是次要机制。

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