Suppr超能文献

在哈氏红酵母U1和U5小核RNA基因保守序列中的剪接体内含子。

Spliceosomal introns in conserved sequences of U1 and U5 small nuclear RNA genes in yeast Rhodotorula hasegawae.

作者信息

Takahashi Y, Tani T, Ohshima Y

机构信息

Department of Biology, Faculty of Science, Kyushu University, Fukuoka.

出版信息

J Biochem. 1996 Sep;120(3):677-83. doi: 10.1093/oxfordjournals.jbchem.a021465.

Abstract

U1, U2, U4, U5, and U6 small nuclear RNAs are essential for precursor mRNA splicing. We previously found one and four mRNA-type, or spliceosomal introns, in the U2 and U6 genes, respectively, of yeast Rhodotorula hasegawae (Erythrobasidium hasegawianum). We proposed that U2 and U6 RNAs form a catalytic core for precursor mRNA splicing and that the introns in those small nuclear RNA genes may have been acquired through reverse splicing of an intron from a precursor mRNA into a catalytic site in small nuclear RNAs. In the present study, we analyzed U1, U4, and U5 genes in R. hasegawae. One spliceosomal intron was found in the U1 region forming base-pairs with a 5' splice site of a precursor mRNA. The U5 gene has two spliceosomal introns in the region that interacts with 5' and 3' splice sites. In contrast, the gene for U4 RNA, which is released from the spliceosome prior to the first step of the splicing reaction, has no intron. These results lend a further support to the proposed relation between presence and position of an intron in an small nuclear RNA gene and the function of the encoded small nuclear RNA.

摘要

U1、U2、U4、U5和U6小核RNA对于前体mRNA剪接至关重要。我们之前分别在哈氏红酵母(长孢红冬孢酵母)的U2和U6基因中发现了一个和四个mRNA型或剪接体内含子。我们提出,U2和U6 RNA形成了前体mRNA剪接的催化核心,并且那些小核RNA基因中的内含子可能是通过内含子从前体mRNA反向剪接到小核RNA的催化位点而获得的。在本研究中,我们分析了哈氏红酵母中的U1、U4和U5基因。在U1区域发现了一个与前体mRNA的5'剪接位点形成碱基对的剪接体内含子。U5基因在与5'和3'剪接位点相互作用的区域有两个剪接体内含子。相比之下,在剪接反应第一步之前从剪接体释放的U4 RNA基因没有内含子。这些结果进一步支持了小核RNA基因中内含子的存在和位置与所编码的小核RNA功能之间的拟议关系。

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