Yakovlev A G, Ruffo M, Jurka J, Krueger K E
Fidia-Georgetown Institute for the Neurosciences, Georgetown University School of Medicine, Washington, DC 20007, USA.
Gene. 1995 Apr 3;155(2):201-5. doi: 10.1016/0378-1119(94)00817-c.
The third intron of the mitochondrial benzodiazepine receptor (MBR)-encoding gene was sequenced from hamster, mouse and human. The rodent species were found to include an Alu-like sequence, as was first discovered in the rat gene. Differences with the rat intron were evident by an insertion of an additional B1 element in the hamster and the introduction of a complete and two partial B2 sequences in the mouse intron. The human intron contained a cluster of four Alu sequences; however, all of these repetitive elements were found to be in the opposite orientation relative to the Alu-like sequence present in the rodent genes. These findings support the possibility that the rodent Alu-like sequence is a remnant of a retropositional insertion in this gene prior to the divergence of rodent species. Because the human intron does not contain the same Alu remnant, it cannot be concluded that the rodent sequence represents an insertion of a primordial Alu element prior to the divergence of rodent and primate lineages.
对仓鼠、小鼠和人类线粒体苯二氮䓬受体(MBR)编码基因的第三个内含子进行了测序。结果发现啮齿动物物种包含一个类似Alu的序列,这是首次在大鼠基因中发现的。仓鼠内含子中额外插入了一个B1元件,小鼠内含子中引入了一个完整的和两个部分的B2序列,这使得与大鼠内含子的差异很明显。人类内含子包含一组四个Alu序列;然而,所有这些重复元件的方向都与啮齿动物基因中存在的类似Alu序列相反。这些发现支持了这样一种可能性,即啮齿动物类似Alu的序列是该基因在啮齿动物物种分化之前逆转座插入的残余物。由于人类内含子不包含相同的Alu残余物,因此不能得出啮齿动物序列代表啮齿动物和灵长类谱系分化之前原始Alu元件插入的结论。