Burke W D, Calalang C C, Eickbush T H
Mol Cell Biol. 1987 Jun;7(6):2221-30. doi: 10.1128/mcb.7.6.2221-2230.1987.
Two classes of DNA elements interrupt a fraction of the rRNA repeats of Bombyx mori. We have analyzed by genomic blotting and sequence analysis one class of these elements which we have named R2. These elements occupy approximately 9% of the rDNA units of B. mori and appear to be homologous to the type II rDNA insertions detected in Drosophila melanogaster. Approximately 25 copies of R2 exist within the B. mori genome, of which at least 20 are located at a precise location within otherwise typical rDNA units. Nucleotide sequence analysis has revealed that the 4.2-kilobase-pair R2 element has a single large open reading frame, occupying over 82% of the total length of the element. The central region of this 1,151-amino-acid open reading frame shows homology to the reverse transcriptase enzymes found in retroviruses and certain transposable elements. Amino acid homology of this region is highest to the mobile line 1 elements of mammals, followed by the mitochondrial type II introns of fungi, and the pol gene of retroviruses. Less homology exists with transposable elements of D. melanogaster and Saccharomyces cerevisiae. Two additional regions of sequence homology between L1 and R2 elements were also found outside the reverse transcriptase region. We suggest that the R2 elements are retrotransposons that are site specific in their insertion into the genome. Such mobility would enable these elements to occupy a small fraction of the rDNA units of B. mori despite their continual elimination from the rDNA locus by sequence turnover.
两类DNA元件中断了家蚕部分rRNA重复序列。我们通过基因组印迹和序列分析对其中一类元件进行了分析,我们将其命名为R2。这些元件约占家蚕rDNA单位的9%,似乎与在黑腹果蝇中检测到的II型rDNA插入序列同源。家蚕基因组中约存在25个R2拷贝,其中至少20个位于典型rDNA单位内的精确位置。核苷酸序列分析表明,4.2千碱基对的R2元件有一个单一的大开放阅读框,占元件总长度的82%以上。这个1151个氨基酸的开放阅读框的中心区域与逆转录病毒和某些转座元件中的逆转录酶具有同源性。该区域的氨基酸同源性与哺乳动物的移动性L1元件最高,其次是真菌的线粒体II型内含子和逆转录病毒的pol基因。与黑腹果蝇和酿酒酵母的转座元件同源性较低。在逆转录酶区域之外,还发现了L1和R2元件之间另外两个序列同源区域。我们认为R2元件是逆转座子,其插入基因组具有位点特异性。这种移动性将使这些元件能够占据家蚕rDNA单位的一小部分,尽管它们通过序列更新不断从rDNA位点被清除。