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酵母中Ty重组的转录诱导

Transcriptional induction of Ty recombination in yeast.

作者信息

Nevo-Caspi Y, Kupiec M

机构信息

Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Ramat Aviv, Israel.

出版信息

Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12711-5. doi: 10.1073/pnas.91.26.12711.

Abstract

Families of repeated sequences are present in the genomes of all eukaryotes. Little is known about the mechanism(s) that prevents recombination between repeated sequences. In the yeast Saccharomyces cerevisiae, recombination between homologous sequences placed at nonhomologous locations in the genome (ectopic recombination) has been shown to occur at high frequencies for artificially created repeats, but at relatively low frequencies for a natural family of repeated sequences, the Ty family. We have previously shown that a high level of Ty cDNA in the cell causes an increase in the rate of nonreciprocal recombination (gene conversion) of a marked Ty element. In the present study, we show that it is also possible to elevate the rate of recombination of a marked Ty by increasing its transcription. This induction is different from, and acts synergistically to, the one seen upon increased levels of donor Ty cDNA. We show that the induction by transcription does not require the products of the RAD50, RAD51, and RAD57 genes. In contrast, cDNA-mediated recombination is dependent on the product of the RAD51 gene but not on products of the genes RAD50 or RAD57.

摘要

重复序列家族存在于所有真核生物的基因组中。关于阻止重复序列之间发生重组的机制,人们知之甚少。在酿酒酵母中,基因组中非同源位置上的同源序列之间的重组(异位重组),对于人工创建的重复序列而言,已被证明会高频发生,但对于一个天然的重复序列家族——Ty家族而言,发生频率相对较低。我们之前已经表明,细胞中高水平的Ty cDNA会导致一个有标记的Ty元件的非相互重组(基因转换)速率增加。在本研究中,我们表明通过增加有标记的Ty的转录,也有可能提高其重组速率。这种诱导不同于在供体Ty cDNA水平增加时所观察到的诱导,并且与之协同作用。我们表明转录诱导不需要RAD50、RAD51和RAD57基因的产物。相比之下,cDNA介导的重组依赖于RAD51基因的产物,但不依赖于RAD50或RAD57基因的产物。

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