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通过对原核生物和真核生物核糖体5S RNA序列的比较分析得出的普遍结构特征。

Universal structural features of prokaryotic and eukaryotic ribosomal 5S RNA derived from comparative analysis of their sequences.

作者信息

Böhm S, Fabian H, Welfle H

出版信息

Acta Biol Med Ger. 1982;41(1):1-16.

PMID:7113541
Abstract

An extensive comparative analysis of more than fifty available sequences of ribosomal 5S RNA has been made. Both for prokaryotic and eukaryotic 5S RNA a generalized secondary structure is presented which is similar to that suggested by Nishikawa and Takemura modified in few positions only. Both generalized secondary structures contain five main helical regions and a high base-pairing content of about 65 +/- 5%. The general structural architecture of prokaryotic and eukaryotic 5S RNA molecules appears to be very similar with minor modifications within particular subgroups of organisms. Conserved and semiconserved nucleotides are accumulated in the single stranded parts of 5S RNA. Functional importance was suggested for some of these regions; other short conserved nucleotide stretches may be involved in the folding of 5S RNA molecules. In particular, we propose a tertiary base-pairing interaction between the universal invariant GUA sequence (positions 76-78 and 75-77 in prokaryotic and eukaryotic 5S RNA, respectively) and the complementary conserved CPuU sequence (positions 38-40 and 36-38) in a parallel manner. A molecular model of the 5S RNA of human KB cells was constructed, which verifies the proposed tertiary interaction, probably stabilizing the two neighboured helices E and D and a stacking arrangement of the bases in the sequence positions 67-108 (and 70-106) in eukaryotic (and prokaryotic) 5S RNAs, respectively.

摘要

对五十多条核糖体5S RNA的可用序列进行了广泛的比较分析。针对原核生物和真核生物的5S RNA,都给出了一个通用的二级结构,该结构与西川和武村提出的结构相似,只是在少数位置有所修改。这两种通用二级结构都包含五个主要螺旋区域,碱基配对含量较高,约为65±5%。原核生物和真核生物5S RNA分子的总体结构架构似乎非常相似,只是在特定生物亚群中有微小修改。保守和半保守核苷酸聚集在5S RNA的单链部分。其中一些区域被认为具有功能重要性;其他短的保守核苷酸片段可能参与5S RNA分子的折叠。特别是,我们提出了通用不变GUA序列(原核生物和真核生物5S RNA中分别位于76 - 78位和75 - 77位)与互补保守CPuU序列(位于38 - 40位和36 - 38位)之间以平行方式的三级碱基配对相互作用。构建了人类KB细胞5S RNA的分子模型,该模型验证了所提出的三级相互作用,可能稳定了两个相邻的螺旋E和D,以及真核生物(和原核生物)5S RNA中序列位置67 - 108(和70 - 106)处碱基的堆积排列。

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