Osheim Y N, Mougey E B, Windle J, Anderson M, O'Reilly M, Miller O L, Beyer A, Sollner-Webb B
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
J Cell Biol. 1996 Jun;133(5):943-54. doi: 10.1083/jcb.133.5.943.
Enhancers could, in principle, function by increasing the rate of reinitiation on individual adjacent active promoters or by increasing the probability that an adjacent promoter is activated for transcription. We have addressed this issue for the repetitive metazoan rDNA enhancer by microinjecting Xenopus oocytes with enhancer-less and enhancer-bearing genes and determining by EM the frequency that each gene type forms active transcription units and their transcript density. We use conditions where transcription requires the normal rDNA promoter and is stimulated 30-50-fold by the enhancer. (In contrast, at saturating template conditions as used in previous EM studies, an aberrant mode of transcription is activated that is not affected by the rDNA enhancer or by the generally recognized rDNA promoter). The active transcription units on enhancer-less genes are found to be as densely packed with nascent transcripts and polymerases as those on enhancer-bearing genes and on the endogenous rRNA genes. Significantly, the enhancer-bearing genes are approximately 30-50-fold more likely to form such active transcription units than enhancer-less genes, consistent with their amounts of transcript. Complementary studies confirm that the enhancer does not affect elongation rate, the stability of the transcription complex, or transcript half-life. These data demonstrate that the repetitive metazoan rDNA enhancer causes more genes to be actively transcribed and does not alter the reinitiation rate on individual active genes.
原则上,增强子可以通过提高单个相邻活性启动子上的重新起始速率,或者通过增加相邻启动子被激活进行转录的概率来发挥作用。我们通过向非洲爪蟾卵母细胞显微注射无增强子基因和含增强子基因,并通过电子显微镜确定每种基因类型形成活性转录单位的频率及其转录本密度,来研究后生动物重复rDNA增强子的这个问题。我们使用的条件是转录需要正常的rDNA启动子,并且增强子可将其刺激30 - 50倍。(相比之下,在先前电子显微镜研究中使用的饱和模板条件下,会激活一种异常的转录模式,这种模式不受rDNA增强子或普遍认可的rDNA启动子的影响)。结果发现,无增强子基因上的活性转录单位与含增强子基因以及内源性rRNA基因上的活性转录单位一样,都密集地充满了新生转录本和聚合酶。值得注意的是,含增强子基因形成这种活性转录单位的可能性比无增强子基因大约高30 - 50倍,这与其转录本数量一致。补充研究证实,增强子不会影响延伸速率、转录复合物的稳定性或转录本半衰期。这些数据表明,后生动物重复rDNA增强子会使更多基因被积极转录,并且不会改变单个活性基因上的重新起始速率。