Wobus U, Bäumlein H, Bogachev S S, Borisevich I V, Panitz R, Kolesnikov N N
Zentralinstitut für Genetik und Kulturpflanzenforschung, Academy of Sciences, Gatersleben.
Mol Gen Genet. 1990 Jul;222(2-3):311-6. doi: 10.1007/BF00633834.
A 1.7 kb long transposable element called TECth1 was found in the 3' flanking region of a Chironomus thummi Balbiani ring gene. As shown by sequence comparison with a second copy, TECth1 is characterized by a perfect terminal inverted repeat of 17 bp flanked by a duplicated target site of 8 bp, four internal imperfect inverted repeats of 17 to 26 bp and terminal regions of about 0.25 kb with a high number of short direct repeats of the consensus sequence ACTTT or permutated and mutated forms such as TTTAC or ACTAT. The terminal inverted repeats and the 8 bp target site duplication are reminiscent of Drosophila P and hobo elements but no long open reading frame starting with ATG is present, suggesting that the two TECth1 copies studied represent deletion derivatives of a longer element coding for its own transposase. In situ hybridization revealed about 75 labelled sites distributed over all chromosomes with the Balbiani ring locus most strongly labelled. Fifty percent of the sites are specific for a given individual, and these variable sites are often heterozygous for the element.
在摇蚊Balbiani环基因的3'侧翼区域发现了一个名为TECth1的1.7 kb长的转座元件。与第二个拷贝的序列比较表明,TECth1的特征是有一个17 bp的完美末端反向重复序列,两侧是一个8 bp的重复靶位点,四个17至26 bp的内部不完美反向重复序列,以及约0.25 kb的末端区域,其中有大量一致序列ACTTT的短正向重复序列或其置换和突变形式,如TTTAC或ACTAT。末端反向重复序列和8 bp靶位点重复让人联想到果蝇的P元件和hobo元件,但不存在以ATG开头的长开放阅读框,这表明所研究的两个TECth1拷贝代表了一个编码自身转座酶的较长元件的缺失衍生物。原位杂交显示约75个标记位点分布在所有染色体上,其中Balbiani环位点标记最强。50%的位点对特定个体是特异的,这些可变位点的元件通常是杂合的。