Suppr超能文献

人U2小核RNA 3'末端形成所需的序列。

Sequences required for 3' end formation of human U2 small nuclear RNA.

作者信息

Yuo C Y, Ares M, Weiner A M

出版信息

Cell. 1985 Aug;42(1):193-202. doi: 10.1016/s0092-8674(85)80115-x.

Abstract

Xenopus oocytes injected with human U2 snRNA genes synthesize mature U2 as well as a U2 precursor with about 10 extra 3' nucleotides (human pre-U2 RNA). Formation of the pre-U2 3' end requires a downstream element located between position +16 and +37 in the U2 3'-flanking sequence. The distance between this element and the U2 coding region can be increased without affecting formation of the pre-U2 3' end. When the natural sequence surrounding the pre-U2 3' end is changed, novel 3' ends are still generated within a narrow range upstream from the element. The 3' terminal stem-loop of U2 snRNA is not required for pre-U2 3' end formation. A sequence within the 3' element (GTTTN0-3AAAPuNNAGA) is conserved among snRNA genes transcribed by RNA polymerase II. Our results suggest that the 3' ends of pre-U2 RNA and histone mRNA may be generated by related but distinct RNA processing mechanisms.

摘要

注射了人类U2小核RNA基因的非洲爪蟾卵母细胞可合成成熟的U2以及带有大约额外10个3'核苷酸的U2前体(人类前体U2 RNA)。前体U2 3'末端的形成需要位于U2 3'侧翼序列中+16至+37位之间的一个下游元件。该元件与U2编码区之间的距离可以增加,而不会影响前体U2 3'末端的形成。当前体U2 3'末端周围的天然序列发生改变时,新的3'末端仍会在该元件上游的一个狭窄范围内产生。U2小核RNA的3'末端茎环结构对于前体U2 3'末端的形成并非必需。3'元件内的一个序列(GTTTN0 - 3AAAPuNNAGA)在由RNA聚合酶II转录的小核RNA基因中是保守的。我们的结果表明,前体U2 RNA和组蛋白mRNA的3'末端可能由相关但不同的RNA加工机制产生。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验