Tronik D, Ekker M, Rougeon F
LA CNRS 361, Département d'Immunologie, Institut Pasteur, Paris, France.
Gene. 1988 Sep 15;69(1):71-80. doi: 10.1016/0378-1119(88)90379-4.
The two renin genes of the mouse (Ren1 and Ren2) are expressed at different levels in the submaxillary gland (SMG). In contrast to mice, there is no detectable renin gene expression in the rat SMG. To determine the molecular basis for these different levels of renin expression, we have compared the 5'-flanking regions of the rat and mouse genes. The sequence of mouse, but not rat, genes reveals the presence in Ren1 and Ren2 of a large insertion, probably a new class of transposable elements. A second, apparently unrelated shorter insertion is present only in Ren2. Otherwise, the mouse and rat 5'-flanking sequences are well conserved and resemble the corresponding region of the human Ren gene, indicating that the insertions occurred after the separation of the rat and mouse species but before the duplication of the mouse Ren gene. We suggest that these structural differences may have a role in the differential expression of the Ren genes in mice and other animals.
小鼠的两个肾素基因(Ren1和Ren2)在颌下腺(SMG)中的表达水平不同。与小鼠不同,在大鼠颌下腺中未检测到肾素基因表达。为了确定这些不同水平肾素表达的分子基础,我们比较了大鼠和小鼠基因的5'侧翼区域。小鼠基因(而非大鼠基因)的序列显示,Ren1和Ren2中存在一个大的插入片段,可能是一类新的转座元件。另一个明显不相关的较短插入片段仅存在于Ren2中。否则,小鼠和大鼠的5'侧翼序列保守性良好,且与人类肾素基因的相应区域相似,这表明这些插入发生在大鼠和小鼠物种分离之后,但在小鼠Ren基因复制之前。我们认为,这些结构差异可能在小鼠和其他动物中肾素基因的差异表达中起作用。