Yoshioka K, Kanda H, Akiba H, Enoki M, Shiba T
Laboratory of Molecular Biology, School of Hygienic Sciences, Kitasato University, Kanagawa, Japan.
Gene. 1991 Jul 22;103(2):179-84. doi: 10.1016/0378-1119(91)90271-c.
The Drosophila melanogaster transposable element copia is usually 5 kb long with long terminal repeats (LTRs), and its major transcripts are a full-length 5-kb RNA and a 2-kb RNA. We have previously shown that the 2-kb RNA is generated through splicing. Here, we have cloned a genomic intronless copia using an oligodeoxyribonucleotide probe which is specific for the junction of the two exons. The unusual copia is bounded by two LTRs and lacks precisely the intron of the 2-kb copia RNA. Identification of genomic intronless copia strongly suggests that copia transposes through an RNA intermediate. Moreover, we have found that copia virus-like particles (VLPs), in which reverse transcription of copia RNA seems likely to occur, packages the spliced copia RNA much less efficiently than the full-length copia RNA. This result leads to the suggestion that much lower copy number of genomic intronless copia, as compared with that of 'normal' copia, may be responsible for the inefficient packaging of the spliced copia RNA into the VLP.
果蝇转座因子copia通常长5 kb,带有长末端重复序列(LTRs),其主要转录本是一个全长5 kb的RNA和一个2 kb的RNA。我们之前已表明,2 kb的RNA是通过剪接产生的。在此,我们使用了一种针对两个外显子连接处的寡脱氧核糖核苷酸探针克隆了一个基因组无内含子copia。这个不同寻常的copia由两个LTRs界定,且恰好缺少2 kb copia RNA的内含子。基因组无内含子copia的鉴定强烈表明copia是通过RNA中间体进行转座的。此外,我们发现copia病毒样颗粒(VLPs),其中copia RNA的逆转录似乎可能发生,其包装剪接后的copia RNA的效率远低于全长copia RNA。这一结果表明,与“正常”copia相比,基因组无内含子copia的拷贝数低得多,这可能是剪接后的copia RNA包装到VLP中效率低下的原因。