Jensen S, Heidmann T
Unités de Biochimie - Enzymologie et de Physicochimie Macromoléculaire, Institut Gustave, Villejuif, France.
EMBO J. 1991 Jul;10(7):1927-37. doi: 10.1002/j.1460-2075.1991.tb07719.x.
We have marked a cloned Drosophila transposable element--the I element--with an engineered neomycin-containing indicator gene, whose expression is conditioned by passage of the transposon through an RNA intermediate. Mobility of the marked element introduced into Drosophila as a transgene could be detected in vivo, upon in toto selection of developing embryos on G418-containing medium. For resistant individuals, Southern blot analysis and nucleotide sequencing after PCR amplification disclosed transposition of the marked element into new loci, with target site duplications and splicing out of the intron in the indicator gene. It demonstrates that the I element, which is closely related to the widespread mammalian LINEs, transposes through an RNA intermediate, as up to now only conjectured from sequence singularities of this class of 'non-viral retrotransposons'. The developed indicator gene provides a potent new genetic tool for detection and quantitative analysis of retrotransposon mobility and its regulation as it occurs in vivo.
我们用一个经过改造的含新霉素指示基因标记了一个克隆的果蝇转座元件——I元件,该基因的表达取决于转座子通过RNA中间体的过程。作为转基因导入果蝇的标记元件的移动性,在含G418培养基上对发育中的胚胎进行全选时可在体内检测到。对于抗性个体,PCR扩增后的Southern印迹分析和核苷酸测序揭示了标记元件已转座到新位点,并伴有靶位点重复以及指示基因中内含子的剪接。这表明与广泛存在的哺乳动物LINEs密切相关的I元件通过RNA中间体进行转座,到目前为止这仅从这类“非病毒逆转录转座子”的序列特征推测而来。所开发的指示基因提供了一种强大的新遗传工具,用于检测和定量分析逆转录转座子在体内发生的移动性及其调控。