Chalker D L, Sandmeyer S B
Department of Microbiology and Molecular Genetics, College of Medicine, University of California, Irvine 92717.
Genetics. 1990 Dec;126(4):837-50. doi: 10.1093/genetics/126.4.837.
Insertions of the yeast element Ty3 resulting from induced retrotransposition were characterized in order to identify the genomic targets of transposition. The DNA sequences of the junctions between Ty3 and flanking DNA were determined for two insertions of an unmarked element. Each insertion was at position -17 from the 5' end of a tRNA-coding sequence. Ninety-one independent insertions of a marked Ty3 element were studied by Southern blot analysis. Pairs of independent insertions into seven genomic loci accounted for 14 of these insertions. The DNA sequence flanking the insertion site was determined for at least one member of each pair of integrated elements. In each case, insertion was at position -16 or -17 relative to the 5' end of one of seven different tRNA genes. This proportion of genomic loci used twice for Ty3 integration is consistent with that predicted by a Poisson distribution for a number of genomic targets roughly equivalent to the estimated number of yeast tRNA genes. In addition, insertions upstream of the same tRNA gene in one case were at different positions, but in all cases were in the same orientation. Thus, genomic insertions of Ty3 in a particular orientation are apparently specified by the target, while the actual position of the insertion relative to the tRNA-coding sequence can vary slightly.
为了确定转座的基因组靶点,对由诱导逆转录转座产生的酵母元件Ty3插入进行了表征。测定了一个无标记元件的两个插入位点处Ty3与侧翼DNA之间连接的DNA序列。每个插入位点都位于一个tRNA编码序列5'端的-17位置。通过Southern印迹分析研究了一个有标记的Ty3元件的91个独立插入。插入到七个基因组位点的独立插入对占了其中的14个插入。测定了每对整合元件中至少一个成员插入位点侧翼的DNA序列。在每种情况下,插入位点相对于七个不同tRNA基因之一的5'端位于-16或-17位置。Ty3整合两次使用的基因组位点比例与泊松分布预测的比例一致,该分布针对的是数量大致相当于酵母tRNA基因估计数量的一些基因组靶点。此外,在一个案例中,同一个tRNA基因上游的插入位点位于不同位置,但在所有情况下方向相同。因此,Ty3在特定方向上的基因组插入显然由靶点指定,而相对于tRNA编码序列的实际插入位置可能会略有不同。