Neigeborn L, Warner J R
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Nucleic Acids Res. 1990 Jul 25;18(14):4179-84. doi: 10.1093/nar/18.14.4179.
In the yeast Saccharomyces cerevisiae, each of the tandemly repeated ribosomal RNA genes carries a 5S gene within the 'non-transcribed' spacer region. These 5S RNA genes lie between the rDNA enhancer and the promoter of rRNA transcription. Since there is roughly equimolar synthesis of 5S RNA and the 35S rRNA precursor transcript we asked whether the enhancer plays a role in regulating the transcription of 5S RNA. A marked 5S gene was inserted into plasmids designed to test rDNA enhancer function. The enhancer failed to stimulate 5S RNA synthesis even though it stimulated transcription of a distal rRNA test gene greater than 10-fold. This failure is consistent with a model of enhancer function that proposes specific interactions between the enhancer and the 35S rRNA promoter via a looping out of the intervening 5S RNA gene.
在酿酒酵母中,每个串联重复的核糖体RNA基因在“非转录”间隔区内都携带一个5S基因。这些5S RNA基因位于rDNA增强子和rRNA转录启动子之间。由于5S RNA和35S rRNA前体转录本的合成大致等摩尔,我们不禁要问增强子是否在调节5S RNA的转录中发挥作用。将一个标记的5S基因插入到用于测试rDNA增强子功能的质粒中。尽管增强子能将一个远端rRNA测试基因的转录刺激10倍以上,但它未能刺激5S RNA的合成。这一结果与增强子功能模型一致,该模型认为增强子与35S rRNA启动子之间通过中间的5S RNA基因环出而发生特异性相互作用。