Mori I, Benian G M, Moerman D G, Waterston R H
Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110.
Proc Natl Acad Sci U S A. 1988 Feb;85(3):861-4. doi: 10.1073/pnas.85.3.861.
The frequency of movement of Tc1, a 1.6-kilobase transposable element in the nematode Caenorhabditis elegans, is under genetic control, and Tc1 insertion sites are widely but nonrandomly distributed. The usually high frequency of insertions at multiple sites in the gene unc-22 suggested that this gene might be particularly rich in preferred target sites. To discover the features of Tc1 target sites, we have sequenced the sites of seven independent Tc1 transpositions into unc-22 and three other sites. Our comparison of these and two other sites from the literature indicates that in all cases Tc1 integrates at the dinucleotide T-A when it is flanked both 5' and 3' by particular preferred nucleotides. Our analysis revealed the following consensus target for Tc1 integration: G-A-K-A-T-A-T-G-T, in which K = G or T. This target site sequence specificity has implications both for the mechanism of Tc1 transposition and the use of Tc1 in cloning genes by transposon-tagging.
Tc1是线虫秀丽隐杆线虫中一个1.6千碱基对的转座元件,其移动频率受遗传控制,并且Tc1插入位点分布广泛但并非随机分布。在基因unc-22的多个位点通常出现的高频率插入表明,该基因可能特别富含优先靶位点。为了发现Tc1靶位点的特征,我们对七个独立的Tc1插入到unc-22及其他三个位点的位点进行了测序。我们将这些位点与文献中的另外两个位点进行比较,结果表明,在所有情况下,当Tc1两侧5'和3'均为特定优先核苷酸时,它会整合到二核苷酸T-A处。我们的分析揭示了Tc1整合的以下共有靶序列:G-A-K-A-T-A-T-G-T,其中K = G或T。这种靶位点序列特异性对Tc1转座机制以及通过转座子标签法克隆基因中Tc1的使用均有影响。