Tsuda M, Iino T
Laboratory of Genetics, Department of Biology, Faculty of Science, University of Tokyo, Japan.
Mol Gen Genet. 1990 Aug;223(1):33-9. doi: 10.1007/BF00315794.
A 37.5 kb region encompassing a set of the naphthalene degrading genes on the Pseudomonas plasmid NAH7 was found to be transposable only in the presence of the transposase encoded by the Tn1721 subgroup of the class II transposons. This newly identified mobile element, designated Tn4655, contained short (38 bp) terminal inverted repeats which shared extensive sequence homology with those of members of the Tn1721 subgroup. Tn4655 transposed by a two-step process involving formation of the cointegrate followed by its subsequent resolution. In contrast to the defect in the trans-acting factor for the first step, a functional system for the latter step was encoded within a 2.4 kb region in Tn4655. Analysis of deletion and insertion mutants demonstrated that the 2.4 kb region contained the cis-acting (res) site and the gene for a trans-acting factor (resolvase); complementation analysis indicated that Tn4655 resolvase function was not interchangeable with those of other well-studied class II transposons, including the Tn1721 subgroup. Tn4655 had no DNA sequences that were hybridizable with the transposase or resolvase genes of the Tn1721 subgroup.
一个包含假单胞菌质粒NAH7上一组萘降解基因的37.5 kb区域被发现仅在II类转座子Tn1721亚组编码的转座酶存在时才可转座。这个新鉴定出的可移动元件,命名为Tn4655,含有短的(38 bp)末端反向重复序列,与Tn1721亚组成员的末端反向重复序列具有广泛的序列同源性。Tn4655通过两步过程进行转座,第一步涉及共整合体的形成,随后是其分解。与第一步中反式作用因子的缺陷相反,第二步的功能系统由Tn4655中的一个2.4 kb区域编码。对缺失和插入突变体的分析表明,2.4 kb区域包含顺式作用(res)位点和一个反式作用因子(解离酶)的基因;互补分析表明,Tn4655解离酶功能与其他经过充分研究的II类转座子(包括Tn1721亚组)的解离酶功能不可互换。Tn4655没有与Tn1721亚组的转座酶或解离酶基因可杂交的DNA序列。