Gu J, Patton J R, Shimba S, Reddy R
Baylor College of Medicine, Department of Pharmacology, Houston, Texas 77030, USA.
RNA. 1996 Sep;2(9):909-18.
The specific and dynamic RNA:RNA interactions between pre-mRNA and small nuclear RNAs (snRNAs), especially U2, U5, and U6 snRNAs, form the catalytic core and are at the heart of the spliceosome formation. The functionally important regions in the snRNAs correspond to the highly modified regions in snRNAs from human, rat, and plant cells. To better understand the importance of the modifications of snRNAs, we identified and localized the modified nucleotides in the five spliceosomal snRNAs of Schizosaccharomyces pombe cells. Twenty-two modified nucleotides, including base methylations, 2'-O-methylations, and pseudouridines, were found in the five spliceosomal snRNAs. The conservation of modified nucleotides between human and S. pombe snRNAs is striking. In addition, most of the modified nucleotides are in or around positions that form hydrogen bonds with the pre-mRNA or with other snRNAs. The results are consistent with the suggestion that modified nucleotides are clustered around functionally important regions of the spliceosomal snRNAs. These data provide the basis for further functional studies on posttranscriptional modifications in spliceosomal snRNAs.
前体信使核糖核酸(pre-mRNA)与小核核糖核酸(snRNA),尤其是U2、U5和U6 snRNA之间特异性且动态的RNA:RNA相互作用形成了催化核心,是剪接体形成的关键所在。snRNA中功能重要的区域与来自人类、大鼠和植物细胞的snRNA中高度修饰的区域相对应。为了更好地理解snRNA修饰的重要性,我们鉴定并定位了粟酒裂殖酵母细胞五种剪接体snRNA中的修饰核苷酸。在这五种剪接体snRNA中发现了22种修饰核苷酸,包括碱基甲基化、2'-O-甲基化和假尿苷。人类和粟酒裂殖酵母snRNA之间修饰核苷酸的保守性十分显著。此外,大多数修饰核苷酸位于与前体信使核糖核酸或其他snRNA形成氢键的位置或其周围。这些结果与修饰核苷酸聚集在剪接体snRNA功能重要区域周围的观点一致。这些数据为进一步研究剪接体snRNA转录后修饰的功能提供了基础。