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通过DNA测序确定噬菌体λ附着位点部分缺失突变体的端点

Determination of the endpoints of partial deletion mutants of the attachment site of bacteriophage lambda by DNA sequencing.

作者信息

Davies R W, Schreier P H, Büchel D E

出版信息

Nucleic Acids Res. 1978 Sep;5(9):3209-18. doi: 10.1093/nar/5.9.3209.

Abstract

The deletion mutants b508 and b522 of bacteriophage lambda both end within the attachment site. The formation of such deletions is dependent upon the presence of intact integrase, and thus the deletion endpoints may be related to the normal crossover site in site-specific recombination. We have determined the DNA sequences of the attachment site regions of these deletions. Comparison of the sequences with lambda wildtype shows that both the deletions end within the central common homology region but at different positions. The consequences of these findings for current models of site-specific recombination are discussed.

摘要

噬菌体λ的缺失突变体b508和b522都在附着位点内终止。此类缺失的形成依赖于完整整合酶的存在,因此缺失端点可能与位点特异性重组中的正常交叉位点有关。我们已经测定了这些缺失的附着位点区域的DNA序列。将这些序列与λ野生型进行比较表明,这两个缺失都在中央共同同源区域内终止,但位置不同。本文讨论了这些发现对当前位点特异性重组模型的影响。

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