Sommer H, Cullum J, Saedler H
Mol Gen Genet. 1979 Aug;175(1):53-6. doi: 10.1007/BF00267855.
The sequence of two new IS2 alleles with promoter activity (IS2-43 and IS2-44) is reported. The alleles are identical and are formed by a 17 bp tandem duplication in an AT-rich region of IS2. This created a new RNA polymerase binding site. A mutation was found that increased the frequency of formation of these 17 bp duplications but not of another class of duplications, the "mini-insertions". This suggested that the mechanisms of formation of the two classes of duplications are different.
报道了两个具有启动子活性的新IS2等位基因(IS2-43和IS2-44)的序列。这些等位基因是相同的,由IS2富含AT区域中的17bp串联重复形成。这产生了一个新的RNA聚合酶结合位点。发现一个突变增加了这些17bp重复形成的频率,但没有增加另一类重复“小插入”的频率。这表明两类重复的形成机制是不同的。