Jeppesen C, Stebbins-Boaz B, Gerbi S A
Brown University, Division of Biology and Medicine, Providence, RI 02912.
Nucleic Acids Res. 1988 Mar 25;16(5):2127-48. doi: 10.1093/nar/16.5.2127.
Using a combination of RNA sequencing and construction of cDNA clones followed by DNA sequencing, we have determined the primary nucleotide sequence of U3 snRNA in Xenopus laevis and Xenopus borealis. This molecule has a length of 219 nucleotides. Alignment of the Xenopus sequences with U3 snRNA sequences from other organisms reveals three evolutionarily conserved blocks. We have probed the secondary structure of U3 snRNA in intact Xenopus laevis nuclei using single-strand specific chemical reagents; primer extension was used to map the positions of chemical modification. The three blocks of conserved sequences fall within single-stranded regions, and are therefore accessible for interaction with other molecules. Models of U3 snRNA function are discussed in light of these data.
通过结合RNA测序、构建cDNA克隆并随后进行DNA测序,我们确定了非洲爪蟾和北美爪蟾中U3小核RNA的初级核苷酸序列。该分子长度为219个核苷酸。将爪蟾序列与其他生物的U3小核RNA序列进行比对,发现了三个进化上保守的区域。我们使用单链特异性化学试剂探测了完整非洲爪蟾细胞核中U3小核RNA的二级结构;采用引物延伸法来定位化学修饰的位置。这三个保守序列区域位于单链区域内,因此可与其他分子相互作用。根据这些数据对U3小核RNA的功能模型进行了讨论。