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测量嵌入酵母人工染色体(YAC)载体中的两个同源DNA片段之间的重组频率。

Measurement of recombination frequencies between two homologous DNA segments embedded in a YAC vector.

作者信息

Yasui H, Kurosawa Y

机构信息

Institute for Comprehensive Medical Science, Fujita Health University, Aichi, Japan.

出版信息

Gene. 1993 Jul 15;129(1):135-9. doi: 10.1016/0378-1119(93)90709-c.

Abstract

We measured the frequencies of recombination in a yeast host between two homologous segments of DNA that had been inserted with the same polarity in a yeast artificial chromosome (YAC) vector. Three kinds of YAC clones were constructed in which the gene encoding neomycin(Nm) resistance was sandwiched between two homologous segments of DNA, such as the IS3 elements of Escherichia coli or human Alu sequences. Frequencies of homologous recombination in yeast were measured in terms of loss of resistance to Nm. In the case of IS3 fragments, homologous recombination between them did occur at a relatively high frequency (5 x 10(-4). In contrast, recombination between two Alu sequences did not occur at a detectable level during a 30-day incubation. Thus, the frequency was less than 10(-5). These results indicate that the Alu sequences do not sufficiently promote the frequency of recombination between two homologous fragments in yeast as to induce rearrangements of DNA in a substantial fraction of YAC clones in libraries.

摘要

我们测量了在酵母宿主中,插入酵母人工染色体(YAC)载体时具有相同极性的两个同源DNA片段之间的重组频率。构建了三种YAC克隆,其中编码新霉素(Nm)抗性的基因夹在两个同源DNA片段之间,如大肠杆菌的IS3元件或人类Alu序列。通过对Nm抗性的丧失来测量酵母中同源重组的频率。对于IS3片段,它们之间的同源重组确实以相对较高的频率发生(5×10⁻⁴)。相比之下,在30天的培养过程中,两个Alu序列之间的重组在可检测水平上未发生。因此,频率小于10⁻⁵。这些结果表明,Alu序列不足以促进酵母中两个同源片段之间的重组频率,从而在文库中相当一部分YAC克隆中诱导DNA重排。

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