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Genetic recombination: recA protein promotes homologous pairing between duplex DNA molecules without strand unwinding.

机译:遗传重组:recA蛋白可促进双链DNA分子之间的同源配对,而不会解链。

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摘要

The recA protein of Escherichia coli promotes pairing in vitro between covalent circular duplex DNA and homologous circular duplex DNA containing a single stranded region. We have used a filter binding assay to investigate the frequency of homologous pairing between gapped and intact duplex DNA when unwinding of the free 3' and 5' ends of the gapped molecules was blocked. In order to obtain DNA without free ends, the gapped DNA was treated with trimethylpsoralen and 360 nm light so as to introduce about 6 crosslinks per DNA molecule and the double stranded regions on either side of the gaps were then digested up to the first crosslinks with exonuclease III and lambda exonuclease. This treatment did not diminish the frequency of homologous pairing, an observation which is difficult to reconcile with models for recombination requiring strand unwinding before pairing.
机译:大肠杆菌的recA蛋白在体外促进共价环状双链DNA和含有单链区域的同源环状双链DNA之间的配对。我们已经使用了过滤器结合实验来研究当缺口分子的自由3'和5'末端的展开被阻止时,缺口和完整双链DNA之间同源配对的频率。为了获得没有自由端的DNA,用三甲基补骨脂素和360 nm的光处理缺口的DNA,以便每个DNA分子引入约6个交联键,然后将缺口两侧的双链区消化成第一个交联键。核酸外切酶III和λ核酸外切酶。这种处理并没有减少同源配对的频率,这一发现很难与配对之前需要解链的重组模型相吻合。

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