Zhuang Y, Weiner A M
Cell. 1986 Sep 12;46(6):827-35. doi: 10.1016/0092-8674(86)90064-4.
Indirect evidence suggests that the 5' end of U1 snRNA recognizes the 5' splice site in mRNA precursors by complementary base pairing. To test this hypothesis, we asked whether point mutations in the alternative 12S and 13S 5' splice sites of the adenovirus E1A gene can be suppressed by compensatory base changes in human U1 snRNA. When the mutant E1A and U1 genes are contransfected into HeLa cells, we observe efficient suppression of one mutation at position +5 in the 12S splice site, but exceedingly weak suppression of another mutation at position +3 in the 13S splice site. These and other results suggest that base pairing between U1 and the 5' splice site is necessary but not sufficient for the splicing of mRNA precursors.
间接证据表明,U1 snRNA的5'端通过互补碱基配对识别mRNA前体中的5'剪接位点。为了验证这一假设,我们探究了腺病毒E1A基因的替代性12S和13S 5'剪接位点中的点突变是否能被人U1 snRNA中的补偿性碱基变化所抑制。当将突变的E1A和U1基因共转染到HeLa细胞中时,我们观察到12S剪接位点中+5位置的一个突变得到了有效抑制,但13S剪接位点中+3位置的另一个突变的抑制作用极其微弱。这些结果以及其他结果表明,U1与5'剪接位点之间的碱基配对对于mRNA前体的剪接是必要的,但并不充分。