Moschetti R, Marsano R M, Barsanti P, Caggese C, Caizzi R
Sezione di Genetica, Dipartimento di Anatomia Patologica e di Genetica, Università di Bari, Via G. Amendola 165/A, 70126 Bari, Italy.
Mol Genet Genomics. 2004 May;271(4):394-401. doi: 10.1007/s00438-004-1007-7. Epub 2004 Apr 2.
Foldback ( FB) elements are transposable elements found in many eukaryotic genomes; they are thought to contribute significantly to genome plasticity. In Drosophila melanogaster, FBs have been shown to be involved in the transposition of large chromosomal regions and in the genetic instability of some alleles of the white gene. In this report we show that FB mediated transposition of w(67C23), a mutation that deletes the promoter of the white gene and its first exon, containing the start codon, can restore expression of the white gene. We have characterized three independent events in which a 14-kb fragment from the w(67C23) locus was transposed into an intron region in three different genes. In each case a local promoter drives the expression of white, producing a chimeric mRNA. These findings suggest that, on an evolutionary timescale, FB elements may contribute to the creation of new genes via exon shuffling.
回文(FB)元件是在许多真核生物基因组中发现的可转座元件;它们被认为对基因组可塑性有重大贡献。在黑腹果蝇中,FB已被证明参与大染色体区域的转座以及白色基因某些等位基因的遗传不稳定性。在本报告中,我们表明,FB介导的w(67C23)转座,即一种缺失白色基因启动子及其包含起始密码子的第一个外显子的突变,能够恢复白色基因的表达。我们对三个独立事件进行了表征,其中来自w(67C23)位点的一个14 kb片段被转座到三个不同基因的内含子区域。在每种情况下,一个局部启动子驱动白色基因的表达,产生嵌合mRNA。这些发现表明,在进化时间尺度上,FB元件可能通过外显子洗牌促成新基因的产生。