Branlant C, Krol A, Ebel J P, Gallinaro H, Lazar E, Jacob M
Nucleic Acids Res. 1981 Feb 25;9(4):841-58. doi: 10.1093/nar/9.4.841.
Chicken, rat and human U1A RNAs in solution, were examined for secondary structure, using several methods including hydrolysis by various nucleases, hybridization to DNA oligomers and analysis of fragment interactions. The experimental results showed that the three U1A RNAs have the same structure, stable over a wide range of pH and ionic conditions. They allowed the selection of one out of several possible models constructed from the data of primary structure. This model is characterized by 4 hairpins and two single-stranded regions, the two hairpins from the 3' part of the molecule bearing very stable stems. In addition, the experimental results showed that in contrast to the 5' half of the molecule, the 3' half has a compact conformation probably stabilized by tertiary interactions. The 5' end of U1A RNA is accessible and free of base-pairing so that it might base-pair with regions of other RNA molecules, for instance, with the extremities of introns as has been recently proposed in a model of splicing.
对溶液中的鸡、大鼠和人类U1A RNA进行了二级结构检测,采用了多种方法,包括用各种核酸酶水解、与DNA寡聚物杂交以及片段相互作用分析。实验结果表明,这三种U1A RNA具有相同的结构,在广泛的pH和离子条件下都很稳定。根据一级结构数据构建的几种可能模型中,它们能确定其中一种。该模型的特征是有4个发夹结构和两个单链区域,分子3'部分的两个发夹结构具有非常稳定的茎。此外,实验结果表明,与分子的5'半部分不同,3'半部分具有紧凑的构象,可能通过三级相互作用得以稳定。U1A RNA的5'端易于接近且没有碱基配对,因此它可能与其他RNA分子的区域进行碱基配对,例如,正如最近在剪接模型中所提出的,与内含子的末端进行碱基配对。