Suppr超能文献

U2小核RNA的一级和二级结构

Primary and secondary structure of U2 snRNA.

作者信息

Reddy R, Henning D, Epstein P, Busch H

出版信息

Nucleic Acids Res. 1981 Nov 11;9(21):5645-58. doi: 10.1093/nar/9.21.5645.

Abstract

With the improved rapid sequencing techniques, the earlier sequence of U2 RNA of Novikoff hepatoma (Shibata et al, J. Biol. Chem. 250, 3909-3920, 1975) was reanalyzed and modified. The improved sequence of U2 RNA is 188 (or 189) nucleotides long and is in register with a characterized U2 RNA pseudogene (Denison et al, PNAS 78, 810-814, 1981) except for an 11 nucleotide sequence (nucleotides 147-157) which is absent from the pseudogene. From these results, a secondary structure of U2 RNA is proposed which is supported by the preferred cleavage sites with T1-RNase, RNase A and S1 nuclease. Isolated U2 RNA was cleaved by T1-RNase preferentially at positions 64 and 164, whereas U2 RNA in U2-snRNP was cleaved only at position 64, indicating that position 164 is protected in U2-snRNP. As with U1 RNA (Epstein et al, PNAS 78, 1562-1566, 1981) the 5'-end of isolated U2 RNA was not preferentially cleaved by T1-RNase.

摘要

随着快速测序技术的改进,对诺维科夫肝癌U2 RNA的早期序列(柴田等人,《生物化学杂志》250,3909 - 3920,1975)进行了重新分析和修正。改进后的U2 RNA序列长度为188(或189)个核苷酸,除了一个11个核苷酸的序列(核苷酸147 - 157)在假基因中不存在外,与一个已鉴定的U2 RNA假基因(丹尼森等人,《美国国家科学院院刊》78,810 - 814,1981)相符。基于这些结果,提出了U2 RNA的二级结构,该结构得到了T1 - 核糖核酸酶、核糖核酸酶A和S1核酸酶的优先切割位点的支持。分离的U2 RNA在T1 - 核糖核酸酶作用下优先在64位和164位被切割,而U2 - snRNP中的U2 RNA仅在64位被切割,这表明164位在U2 - snRNP中受到保护。与U1 RNA(爱泼斯坦等人,《美国国家科学院院刊》78,1562 - 1566,1981)一样,分离的U2 RNA的5'端在T1 - 核糖核酸酶作用下没有被优先切割。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d92/327549/b087f379a62e/nar00414-0144-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验