Roeder G S, Smith M, Lambie E J
Mol Cell Biol. 1984 Apr;4(4):703-11. doi: 10.1128/mcb.4.4.703-711.1984.
In this paper, we describe the movement of a genetically marked Saccharomyces cerevisiae transposon. Ty912(URA3), to new sites in the S. cerevisiae genome. Ty912 is an element present at the HIS4 locus in the his4-912 mutant. To detect movement of Ty912, this element has been genetically marked with the S. cerevisiae URA3 gene. Movement of Ty912(URA3) occurs by recombination between the marked element and homologous Ty elements elsewhere in the S. cerevisiae genome. Ty912(URA3) recombines most often with elements near the HIS4 locus on chromosome III, less often with Ty elements elsewhere on chromosome III, and least often with Ty elements on other chromosomes. These recombination events result in changes in the number of Ty elements present in the cell and in duplications and deletions of unique sequence DNA.
在本文中,我们描述了一个带有遗传标记的酿酒酵母转座子Ty912(URA3)在酿酒酵母基因组中转移至新位点的情况。Ty912是his4 - 912突变体中位于HIS4位点的一个元件。为了检测Ty912的转移,该元件已用酿酒酵母URA3基因进行了遗传标记。Ty912(URA3)的转移是通过标记元件与酿酒酵母基因组中其他位置的同源Ty元件之间的重组发生的。Ty912(URA3)最常与III号染色体上靠近HIS4位点的元件重组,较少与III号染色体上其他位置的Ty元件重组,与其他染色体上的Ty元件重组的频率最低。这些重组事件导致细胞中Ty元件数量的变化以及独特序列DNA的重复和缺失。