Labhart P, Reeder R H
Cell. 1984 May;37(1):285-9. doi: 10.1016/0092-8674(84)90324-6.
The spacer region of the Xenopus laevis ribosomal gene contains blocks of repetitive sequence elements that are 60 or 81 bp long. These 60/81 bp elements function as enhancer elements for the RNA polymerase I promoter at the 5' end of the gene. An RNA polymerase I promoter adjacent to a block of 60/81 bp elements is always dominant over a promoter on a second plasmid when both are coinjected into oocyte nuclei. If two promoters are placed on the same plasmid containing enhancers, both promoters come under their influence and are codominant. The influence of the enhancers can be transmitted through several kilobases of plasmid sequence, through a potentially active promoter, and is independent of the orientation of the enhancers. The enhancers appear to compete with promoters for the same transcription factor(s); however, the enhancers can only compete when they are on a circular plasmid.
非洲爪蟾核糖体基因的间隔区包含长度为60或81 bp的重复序列元件块。这些60/81 bp元件作为基因5'端RNA聚合酶I启动子的增强子元件发挥作用。当将与60/81 bp元件块相邻的RNA聚合酶I启动子和第二个质粒上的启动子共注射到卵母细胞核中时,前者总是占主导地位。如果将两个启动子置于含有增强子的同一质粒上,两个启动子都会受到其影响并呈共显性。增强子的影响可以通过质粒序列的几千个碱基、通过一个潜在活跃的启动子进行传递,并且与增强子的方向无关。增强子似乎与启动子竞争相同的转录因子;然而,增强子只有在位于环状质粒上时才能竞争。