Courage-Tebbe U, Döring H P, Fedoroff N, Starlinger P
Cell. 1983 Sep;34(2):383-93. doi: 10.1016/0092-8674(83)90372-0.
We have analyzed the structure of the Shrunken (Sh) locus in a strain containing an unstable recessive mutation, sh-m5933, caused by the transposable controlling element Dissociation (Ds). We have also analyzed nine spontaneous Sh revertant alleles. The sh-m5933 allele contains a 30 kb insertion at the Sh locus, as well as a duplication that includes part of the insertion and the Sh locus sequence on the 5' side of the insertion site. The revertants continue to show Ds-mediated chromosome breakage at the Sh locus, have an intact Sh locus from which the insertion has been excised, and retain the duplication. One of the nine revertant alleles has a 2 kb deletion at the junction between the Sh locus and the insertion sequence in the duplicated segment of the locus. The revertant also shows a temporal change in the pattern of somatic chromosome breakage, implicating the junction sequence as the site of Ds-mediated chromosome breakage.
我们分析了一个含有不稳定隐性突变sh-m5933的品系中皱缩(Sh)基因座的结构,该突变由转座控制元件解离(Ds)引起。我们还分析了九个自发的Sh回复等位基因。sh-m5933等位基因在Sh基因座处有一个30 kb的插入,以及一个重复序列,该重复序列包括插入序列的一部分和插入位点5'侧的Sh基因座序列。回复体在Sh基因座处继续表现出Ds介导的染色体断裂,具有一个完整的Sh基因座,插入序列已从该基因座切除,并保留了重复序列。九个回复等位基因中的一个在基因座重复片段中Sh基因座与插入序列的连接处有一个2 kb的缺失。该回复体在体细胞染色体断裂模式上也表现出时间变化,这表明连接序列是Ds介导的染色体断裂位点。