Michels P A, Bernards A, Van der Ploeg L H, Borst P
Nucleic Acids Res. 1982 Apr 10;10(7):2353-66. doi: 10.1093/nar/10.7.2353.
We have analysed the gene for variant surface glycoprotein 118 in eight independent clones of Trypanosoma brucei, two of which express the 118 gene. Expression of this gene is strictly coupled to the presence of an extra copy of the gene. In both clones the expression-linked copy is transposed to the same (or a very similar) expression site elsewhere in the genome, but the length of the sequences flanking the transposed segment in the expression site differs markedly. By means of S1 nuclease protection experiments we demonstrate that the 3'-ends of the messenger RNAs for variant surface glycoproteins 118a and 118b are different, in agreement with the hypothesis that the generation of an expression-linked copy involves a recombination between the 3' segment of the basic gene copy and a homologous region present in the expression site.
我们分析了布氏锥虫八个独立克隆中的变异表面糖蛋白118基因,其中两个克隆表达该118基因。该基因的表达与基因的额外拷贝的存在严格相关。在这两个克隆中,与表达相关的拷贝都转座到基因组中其他位置的相同(或非常相似)的表达位点,但表达位点中转座片段两侧的序列长度明显不同。通过S1核酸酶保护实验,我们证明变异表面糖蛋白118a和118b的信使核糖核酸的3'末端不同,这与以下假设一致:与表达相关的拷贝的产生涉及基本基因拷贝的3'片段与表达位点中存在的同源区域之间的重组。