Hernandez N, Lucito R
Cold Spring Harbor Laboratory, NY 11724.
EMBO J. 1988 Oct;7(10):3125-34. doi: 10.1002/j.1460-2075.1988.tb03179.x.
Formation of the human U1 and U2 snRNA 3' ends requires both a conserved sequence, the 3' box, located downstream of the snRNA termini and sequences within the snRNA promoter regions. Indeed, replacement of the U1 snRNA promoter by mRNA promoters inhibits U1 3' end formation. We have now mutated the 5' flanking region of the human U2 gene and assayed the effects on initiation of transcription and 3' end formation. The 5' flanking region of the U2 gene contains two major promoter elements, a previously characterized distal element that enhances the efficiency of transcription and a proximal element, which our analysis localizes between positions -59 and -43 in a segment conserved in vertebrate snRNA genes. The 5' flanking region does not contain an element required solely for 3' end formation. However, when enhancer elements from an mRNA-encoding gene are introduced into a U2 promoter lacking its distal element, 3' end formation is inhibited. Together, these results suggest that the U2 promoter elements themselves are involved in 3' end formation, presumably by directing the formation of a unique transcription complex which is compatible with 3' end formation at the 3' box. Alteration of the composition of this transcription complex results in increased read-through at the 3' box.
人类U1和U2小核RNA(snRNA)3'末端的形成既需要一个保守序列(位于snRNA末端下游的3'框),也需要snRNA启动子区域内的序列。实际上,用mRNA启动子替换U1 snRNA启动子会抑制U1 3'末端的形成。我们现在已经对人类U2基因的5'侧翼区域进行了突变,并检测了其对转录起始和3'末端形成的影响。U2基因的5'侧翼区域包含两个主要的启动子元件,一个是先前已表征的增强转录效率的远端元件,另一个是近端元件,我们的分析将其定位在脊椎动物snRNA基因保守片段中-59至-43位之间。5'侧翼区域不包含仅用于3'末端形成所需的元件。然而,当将来自编码mRNA的基因的增强子元件引入缺乏其远端元件的U2启动子时,3'末端的形成会受到抑制。总之,这些结果表明,U2启动子元件本身参与了3'末端的形成,大概是通过指导形成一种独特的转录复合物,该复合物与3'框处的3'末端形成兼容。这种转录复合物组成的改变会导致在3'框处通读增加。